Guidelines-for-safe-and-effective-NPT-2021-update.pdf

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Guidelines for safe and effective
near-patient testing (NPT)
2021 Update
Approved for soft release by the National Near-Patient Testing (NPT) Consultative Group, Dublin, Ireland
April 21, 2021
(This version 6.2 is valid until April 21, 2022)

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Table of contents
Foreword ................................................................................................................................................ 5
National NPT consultative group membership..................................................................................... 6
Version control....................................................................................................................................... 6
Glossary and abbreviations.................................................................................................................... 7
Chapter 1. Executive summary and recommendations for safe and effective NPT ..........................10
1.1 Overall aims of this Guideline.....................................................................................................10
1.2 Scope...........................................................................................................................................10
1.3 Key recommendations ................................................................................................................11
1.4 Definition of NPT.........................................................................................................................11
1.5 Accreditation of NPT...................................................................................................................12
1.6 Requirements for safe and effective NPT...................................................................................13
1.7 Conclusion...................................................................................................................................18
1.8 Chapter references .....................................................................................................................19
Chapter 2. Definition, uses and risk/benefit analysis for NPT............................................................20
2.1 Definition of NPT.........................................................................................................................20
2.2 Existing and emerging uses for NPT............................................................................................20
2.3 Risks and benefits of NPT and the need for confirmatory testing..............................................22
2.4 Unnecessary testing and financial risks ......................................................................................22
Chapter 3. Governance and management of NPT services: the role of the NPT steering group ......24
3.1 Responsibility for NPT services ...................................................................................................24
3.2 Terms of reference of the NPT steering group ...........................................................................25
3.3 NPT steering group membership................................................................................................25
3.4 Responsibilities of the NPT steering group.................................................................................26
3.5 Governance issues and the IVD industry ....................................................................................28

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3.6 Primary care................................................................................................................................28
3.7 Community pharmacists .............................................................................................................28
Chapter 4. Commissioning NPT services..............................................................................................29
4.1 Case of need and business case..................................................................................................29
4.2 Resources....................................................................................................................................30
4.3 Space...........................................................................................................................................31
Chapter 5. Implementing NPT services ...............................................................................................32
5.1 NPT operational teams ...............................................................................................................32
5.2 The role of the NPT operational team ........................................................................................32
5.3 Validation and verification of NPT IVDs......................................................................................33
5.4 Developing standard operating procedures for NPT ..................................................................34
5.5 Training .......................................................................................................................................34
5.6 Competence/proficiency testing of NPT operators....................................................................36
5.7 Quality assurance programme....................................................................................................36
5.8 Internal quality control ...............................................................................................................37
5.9 External quality assurance ..........................................................................................................37
5.10 Recording of results and audit trail...........................................................................................37
5.11 Reviewing results ......................................................................................................................37
5.12 Traceability and recall...............................................................................................................38
5.13 Maintenance and service..........................................................................................................39
5.14 Retention of records .................................................................................................................39
5.15 Health and safety......................................................................................................................39
5.16 Chapter references ...................................................................................................................40
Chapter 6. Regulatory requirements for NPT IVDs: the role of the HPRA .........................................41
6.1 The IVD Directive 98/79/EC and the IVD Regulation 2017/746/EU............................................41
6.2 Risk assessment of IVDs used for NPT ........................................................................................42
6.3 Key changes under the new IVD Regulation...............................................................................42
6.4 Clinical data supporting safety and performance of IVDs ..........................................................43
6.5 HPRA safety notices, HPRA information notices and manufacturer field safety notices ...........43

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6.6 Adverse incident reporting .........................................................................................................44
6.7 Unique device identification (UDI)..............................................................................................44
Chapter 7. ICT connectivity for NPT.....................................................................................................46
7.1 Connectivity and the national medical laboratory information system (MedLIS)......................46
7.2 Use of ICT for generating clinical alerts ......................................................................................48
Chapter 8. Implementing NPT in primary and community care settings...........................................50
8.1 Clinical and managerial governance of NPT outside of hospital settings...................................50
8.2 Recommendations for safe and effective NPT outside of hospital settings...............................51
8.3 Self-audit checklist ......................................................................................................................51
8.4 Training and competency assessment........................................................................................51
8.5 Premises......................................................................................................................................51
8.6 Recent organisational developments in the primary care sector...............................................53
8.7 Pharmacies..................................................................................................................................53
Concluding remarks..............................................................................................................................54
Bibliography..........................................................................................................................................55
Appendices ...........................................................................................................................................57
1 NPT steering group template.........................................................................................................57
2 User application form for a new NPT service ................................................................................59
3 Cost benefit analysis form..............................................................................................................63
4 Implementation checklist for an approved NPT service................................................................65
5 Patient evaluation form template (for non-GP based NPT settings).............................................72
6 GP referral letter template (for non-GP based NPT settings)........................................................73
7 NPT primary/community care checklist.........................................................................................74
8 Training record templates..............................................................................................................77

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Foreword
The National Near-Patient Testing (NPT) Consultative Group have been revising the Irish National
Near-Patient Testing Guidelines over the past two years. Due to the unique circumstances of the
coronavirus pandemic, we released a final Beta-Version on April 20, 2020 in the interests of having
an updated authoritative guideline available and to provide an opportunity for early feedback.
Further updates are now included in this version released on April 21, 2021 which is valid until
April 21, 2022. Comments on this version should be emailed to pathology@rcpi.ie.
Near-patient testing (NPT) aims to improve patient outcomes through provision of a laboratory
medicine service by healthcare professionals using small analytical devices provided near to the
patient rather than from a clinical laboratory.
The first Irish NPT guidelines were published in 2007 in two separate booklets covering hospital
settings and primary and community care. Terminology has also moved full-cycle with the term NPT
now re-introduced and replacing point of care testing (POCT) in the EU’s latest IVD Regulation. This
updated guideline uses the term NPT throughout, and it also covers all healthcare sectors in a single
guideline. Patient self-testing is not covered by the term “NPT” and is excluded from this guideline.
The present and previous Irish guidelines stem from the work of the National NPT Consultative
Group which convenes under the auspices of the Faculty of Pathology of the Royal College of
Physicians of Ireland and represents national laboratory medicine organisations and regulatory
bodies with an interest in NPT. Originally founded in 2006, this group now includes representatives
from the Faculty of Pathology of the Royal College of Physicians of Ireland, the Association of Clinical
Biochemists in Ireland, and the Academy of Clinical Science and Laboratory Medicine. The Health
Products Regulatory Authority (the regulator for medical devices and IVDs in Ireland) and the
pharmacy regulator (the Pharmaceutical Society of Ireland) are also represented. The National
Clinical Programme in Pathology has been represented by both its former and current clinical leads.
The terms of reference of the group are to maintain guidelines for safe and effective NPT in Ireland
and to disseminate the guidelines to the major stakeholders. The group also conducts surveys on
NPT including compliance with the guidelines. This revision of the guidelines is timely given the
recent updates to ISO 22870 in 2016, the imminent implementation of the new IVD Regulation
2017/746/EU in 2022, the introduction of NPT accreditation to ISO 15189/22870 standards by the
Irish National Accreditation Board, and the expected roll-out of the national medical laboratory
information system (MedLIS) in 2021.
These guidelines should be adopted by those responsible for NPT in Irish hospitals, to ensure that
risks to patient health and safety are minimised. Given the active development of primary care
centres with potential for on-site diagnostics capability, a framework for primary and community
care organisations, community pharmacists and the IVD industry is also included.
Finally, I wish to thank the current and past members of the consultative group who gave their time
generously and patiently during the original production and subsequent revision of these guidelines.
Gerard Boran
Chairperson, on behalf of the NPT Consultative Group, April 21, 2021

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National NPT consultative group membership
Paudy O’Gorman, Academy of Clinical Science and Laboratory Medicine
Bernadette Jackson, Academy of Clinical Science and Laboratory Medicine
Ruth O’Kelly, Association of Clinical Biochemists in Ireland
Paula O’Shea, Association of Clinical Biochemists in Ireland
Mary Keogan, National Clinical Programme in Pathology
Mari Fitzgerald, National Clinical Programme in Pathology
Anne Mannion, National Clinical Programme in Pathology
Orla Carroll, Pharmaceutical Society of Ireland
Patricia Howley, Irish External Quality Assessment Scheme
Anne Kane, Irish External Quality Assessment Scheme
Avril Aylward, Health Products Regulatory Authority
Karina O’Connell, Irish Society of Clinical Microbiologists
Richard Walsh, National Acute Medicine Programme, HSE
Rama Srinivasan, RCPI Faculty of Pathology
Gerard Boran, RCPI Faculty of Pathology (chair)
April 21, 2021
Version control
Soft Release (Beta) Version 5.7, released April 20, 2020. Valid until April 20, 2021
Soft Release Version 6.2, released April 21, 2021. Valid until April 21, 2022

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Glossary and abbreviations
CAP College of American Pathologists
CE Mark The CE mark that appears on an IVD or on its packaging means that the device satisfies
the relevant essential requirements of the IVD Directive 98/79/EC and is fit for its
intended purpose as specified by the manufacturer. Under the IVDR, the ‘CE marking of
conformity’ or ‘CE marking’ means a marking by which a manufacturer indicates that a
device is in conformity with the applicable requirements set out in this Regulation and
other applicable Union harmonisation legislation providing for its affixing.
CEN European Committee for Standardisation
CIC Connectivity Industry Consortium, formed by the IVD industry to address
connectivity solutions for NPT IVDs
CLSI Clinical Laboratory Standards Institute (USA), formerly the National Committee for
Clinical Laboratory Standards.
Competent
Authority
The competent authority is the body which has the authority to act on behalf of the
government of a member state to ensure that the requirements of the Medical
Device Directives / Regulations are carried out in that particular member state.
EN ISO An ISO (International Organisation for Standardisation) standard adopted in
Europe
EQA External Quality Assessment
EU European Union
EUDAMED A centralised electronic system which will allow manufacturers to report serious
incidents and other reportable events. This will also allow the public to be
adequately informed about devices on the European market.
FDA Food and Drugs Administration (USA)
FSCA Field Safety Corrective Action
FSN Field Safety Notice
GDPR General Data Protection Regulations 2016
GP General practitioner
HIV Human immunodeficiency virus
HL7 Health level 7 provides a framework for the exchange, integration, sharing, and
retrieval of electronic health information.

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HPRA Health Products Regulatory Authority
ICT Information and communication technologies
IEEE Institute of Electrical and Electronic Engineers
IEQAS Irish External Quality Assessment Scheme
IFCC International Federation of Clinical Chemistry
IFU Instructions for use
INAB Irish National Accreditation Board
IQC Internal quality control
ISO International Organisation for Standardisation
IVDR In-vitro Diagnostic Medical Device Regulation EU2017/746
IVD In-vitro diagnostic medical device. According to the IVD Directive 98/79/EC an IVD
is defined as any medical device which is a reagent, reagent product, calibrator,
control material, kit, instrument, apparatus, equipment or system, whether used
alone or in combination intended by the manufacturer to be used in vitro for the
examination of specimens, including blood and tissue donations, derived from the
human body, solely or principally for the purpose of providing information:
 concerning a physiological or pathological state, or
 concerning a congenital abnormality, or
 to determine the safety and compatibility with potential recipients, or
 to monitor therapeutic measures
Under the IVD Regulation 2017/746/EU (IVDR) ‘in vitro diagnostic medical
device’ means any medical device which is a reagent, reagent product,
calibrator, control material, kit, instrument, apparatus, piece of equipment,
software or system, whether used alone or in combination, intended by the
manufacturer to be used in vitro for the examination of specimens, including
blood and tissue donations, derived from the human body, solely or
principally for the purpose of providing information on one or more of the
following:
 concerning a physiological or pathological process or state
 concerning congenital physical or mental impairments
 concerning the predisposition to a medical condition or a disease
 to determine the safety and compatibility with potential recipients
 to predict treatment response or reactions
 to define or monitoring therapeutic measures
Specimen receptacles shall also be deemed to be in vitro diagnostic medical
devices.

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JCCLS Japanese Committee of Clinical Laboratory Standards
MedLIS National Medical Laboratory Information System
NIMIS National Integrated Medical Imaging System
NCCLS National Committee for Clinical Laboratory Standards
NPT Near-patient testing
POCT Point of care testing
POCT1-A,
POCT01-A2,
POCT02-A
This is an internationally accepted series of NPT connectivity standards described
in the Clinical and Laboratory Standards Institute (CLSI) Point-of-Care Connectivity
Approved Standard (POCT01-A2, and its predecessor POCT1-A). The standards
were developed by a co-operative effort of providers, manufacturers and
representatives of CLSI, HL7, IEEE, CAP, FDA, JCCLS, and the IFCC. POCT01-A2 is
the latest version of the standard in 2006, and POCT02-A is an implementation
guideline for NPT connectivity standards for healthcare providers released in
2008. As of April 2021, these standards remain valid.
PSI Pharmaceutical Society of Ireland
RICO Regional integrated care organisations
QRG Quick Reference Guide
SOP Standard operating procedure
UDI Unique Device Identifier
USA United States of America
Validation Confirmation, through the provision of objective evidence, that the requirements
for a specific intended use or application have been fulfilled. Examples of when
validation is required could include use of non-standard methods, use of
laboratory designed or developed methods, significant modification to validated
methods, use of standard methods outside their intended scope (such as sample
types not included in manufacturer’s specifications), changes involving new
technology, or significant parameter changes (e.g. reagents, equipment, time,
temperature).
Verification Confirmation, through provision of objective evidence, that specified
requirements have been fulfilled. However, verification is different to validation in
that it is the demonstration of the performance characteristics previously found
during method validation in the laboratory where it is intended to be used.
Verification will demonstrate that a validated method, kit, reagent or equipment
which is used without modification, can be satisfactorily performed by the user,
and meet defined criteria and end user requirements. Examples of when
verification is required could include: implementation of international, regional or
national standard methods, use of manufacturer validated kit, reagent or
equipment, used as specified and without deviation.

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Chapter 1
Executive summary and recommendations for
safe and effective NPT
1.1 Overall aims of this guideline
This document provides guidance for safe and effective NPT, using IVDs that are fit for purpose and
operated by a competent individual on the correct patient, giving quality results which should
become part of the patient record.
1. All NPT in hospital settings should be accredited to ISO 15189/22870 standards and meet
the requirements as described in this guideline.
2. It is strongly recommended that community healthcare facilities including primary care
centres establish a close link with their local hospital pathology service to ensure NPT is
provided in a safe and effective manner and to be ultimately accredited to the required
ISO 15189/22870 standards. This can only be achieved in conjunction with the local
hospital pathology service.
3. Pharmacies providing NPT services should follow the Guidance on the Provision of Testing
Services in Pharmacies from the Pharmaceutical Society of Ireland, and should be aiming
for ISO 15189/22870 accreditation as an ultimate goal.
4. The date of application of the new IVDR is May 2022. The IVDR and role of the HPRA are
described in detail in Chapter 6. The role of the Irish National Accreditation Board (INAB)
in relation to accreditation is also outlined in this chapter.
1.2 Scope
The aim of this document is to provide guidance and recommendations on the implementation and
management of safe and effective NPT in both hospital and community settings.
It is intended to assist those responsible for the delivery of NPT and to ensure that risks to patient
health and safety are minimised. Patient self-testing is not within the scope of this document.

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1.3 Key recommendations
Governance
Commissioning
Implementation
Regulation
1. Establish an NPT Steering Group and organisation-wide NPT Policy
2. Consult with local laboratory
3. Document Case of Need involving all stakeholders
4. Establish an NPT operational team
5. Ensure all IVDs are CE marked, adequately validated and independently verified
6. Develop standard operating procedures and protocols for all NPT
7. Ensure that anyone performing NPT is trained and demonstrated on-going
competence
8. Implement a quality assurance programme, including performance of internal
quality control and external quality assessment for all NPT
9. Ensure patient results are reviewed and interpreted by appropriately qualified
persons
10. Ensure full traceability of all IVDs used, including reagents and consumables*
11. Ensure health and safety, and waste management training for staff*
12. Ensure all IVDs meet national and European IVD legislative requirements*
13. Report adverse incidents to the designated hospital committee, the
manufacturer and the HPRA
14. Include all NPT results in patient’s health record, ideally by implementing ICT
connectivity
* Recommendations 10, 11 and 12 are required for safe implementation of NPT, and are also regulatory requirements
1.4 Definition of NPT
A device for NPT is defined in Article 2 of the IVDR1
as “any device that is not intended for self-
testing but is intended to perform testing outside a laboratory environment, generally near to, or at
the side of, the patient by a health professional”. NPT has replaced POCT as the preferred
terminology in the EU’s IVD Regulation1
. NPT aims to improve patient outcomes through patient
Key Recommendations for Safe and Effective NPT

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testing using small analytical devices (such as test kits, single-use devices and analysers), provided
near to the patient rather than from a central clinical laboratory.
Advances in technology have resulted in compact, easy-to-use IVDs that make it possible to carry out
a range of examinations at, or close to, the patient in either a hospital or community setting. NPT
may improve patient outcomes, test turn-around times and facilitate early decision making.
With the increasing use of NPT it is important that testing performed outside of a central laboratory
is assured of the same quality and standards and does not represent a patient safety risk.
1.5 Accreditation of NPT
Accreditation is the process in which certification of competency, authority, or credibility is
presented and enhances public confidence in medical test results. Standards for accreditation of
medical testing are set by the International Organisation for Standardisation (ISO) and ISO 15189
(Medical Laboratories - Requirements for quality and competence)2
is the standard for laboratories.
ISO 22870 (Point-of-care testing (POCT) - Requirements for quality and competence)3
gives specific
requirements applicable to NPT and is intended to be used in conjunction with ISO 15189.
Increasingly regulators require laboratory tests (European Tissues & Cell Directive 2004/23/EU)4
to
be accredited to ISO 15189. With increasing use of NPT it is important that patients and health care
providers have confidence that NPT results are of similar quality to laboratory tests. NPT can only be
accredited to ISO 22870 in conjunction with ISO 15189.
INAB is the national body with responsibility for accreditation of laboratories and NPT and is the sole
accreditation body for Ireland in line with regulation EC/765/20085
. Its policy for the conduct of NPT
assessment visits is outlined in document PS316
Accreditation of laboratories and NPT ensures that any risk to the patient and to the facility can be
managed by a well-designed, fully implemented quality management system that facilitates:
 evaluation of new or alternative NPT instruments and systems,
 evaluation and approval of end-user proposals and protocols,
 purchase, installation and maintenance of equipment,
 maintenance of consumable supplies and reagents,
 training, certification and recertification of laboratory / NPT system operators,
 quality control and quality assurance,
 connectivity.

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1.6 Requirements for safe and effective NPT
Both national guidelines and ISO standards require that every facility which provides NPT should
have a NPT policy consistent with these guidelines.
There are still significant gaps in accreditation throughout all healthcare sectors, for both NPT and
central laboratory testing. Whereas it is acknowledged that many healthcare facilities are on a
journey towards full accreditation of all laboratory and NPT services, full accreditation is
nevertheless the goal to minimise risk and ensure optimal patient safety.
The advent of the more stringent IVD Regulation 2017/746/EU1
and the imperative to provide safe
and effective pathology services regardless of location or technology used further emphasises this
requirement.
Services in Pharmacies7
from the Pharmaceutical Society of Ireland (updated October
2019), and should be aiming for ISO 15189/22870 accreditation as an ultimate goal.
Recommendation 1: Establish an NPT steering group and organisation-wide NPT policy.
Where NPT services are provided, a system for clinical and managerial governance should be
established including a person designated as responsible and accountable for the service.
- Satisfactory accountability for NPT services is achieved by the establishment of a
multidisciplinary NPT steering group with responsibility to develop and oversee an
organisation-wide NPT policy.
- In hospital settings, the NPT steering group is usually accountable to the executive
management team via the director of pathology and chaired by a laboratory consultant.

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- In all settings, regular consultation and representation from appropriate local laboratory
disciplines (inclusive of all users) play a vital role in this group.
- The NPT steering group should implement a NPT policy to ensure compliance with relevant
legislation, regulations, and current accreditation standards governing the use of NPT
services:
 Relevant European and National legislation,
 Laboratory accreditation standards (EN ISO 15189 and EN ISO 22870),
 HSE requirements, e.g. medical records,
 Risk management requirements,
 Infection control and prevention requirements,
 Data protection regulations.
- NPT service development requests should be evaluated by the NPT steering group to ensure
that clinical need and effectiveness are defined before a NPT service is introduced and that
quality objectives are defined and subsequently evaluated.
- The NPT steering group should review and monitor quality objectives as required and have
the authority to withdraw and/or suspend a service in the event of a safety-related or
performance issue or lack of clinical effectiveness.
Recommendation 2. Consult with local laboratory.
The clinical laboratory is a source of expertise on NPT and has an essential role in the leadership and
co-ordination of NPT, in hospital settings and for local general practitioners (GP). Proposals for new
NPT in the hospital setting should always involve detailed consultation with the local laboratory.
In community and primary care settings, it is advisable that providers of NPT are aware of laboratory
services in their locality which can provide specialist advice and expertise if required.
Communication between the hospital and primary and community care sectors is advised.
- NPT should not be considered when the local laboratory can provide a result in a timely
manner appropriate to the clinical condition.
- Note that confirmatory testing in the local accredited laboratory may be required in certain
conditions (such as for out-of-range or critical NPT results).
Recommendation 3. Document the case of need involving all stakeholders.
A case of need should be prepared by those proposing a new NPT service in conjunction with all
relevant stakeholders including the laboratory. For example, dialogue and close cooperation may be
required between local hospitals, GPs, pharmacies, patients, and representative bodies depending
on the nature of the NPT under consideration to ensure the proposed NPT is fit for purpose and all
patient safety risks have been considered.

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Clear evidence of clinical need and effectiveness must be available before a new NPT service is
introduced. A business case and cost-benefit analysis is also usually required, either as part of or
separate from the case of need.
Recommendation 4. Establish an NPT operational team.
NPT operational team(s) with relevant personnel should be appointed to oversee the day-to-day
operation of NPT. Each operational team must be adequately resourced to enable them to
implement, monitor and audit the day-to-day NPT policy.
Recommendation 5. Ensure all IVDs are CE marked, adequately validated and independently
verified.
In compliance with ISO 15189 test procedures should be subjected to independent verification
before being introduced to provide objective evidence that the test procedure and/or IVD used is fit
for purpose.
-Test methods are verified under conditions of normal use by use of blank samples, control
samples, duplicate samples, calibration checks, IQC monitoring and EQA performance.
- Aspects of verification should include sensitivity and specificity, accuracy and precision,
repeatability, reproducibility, limits of detection, limit of quantitation and comparability to
existing laboratory methods if available.
- Where possible, a backup laboratory method should be available for any NPT to provide
confirmatory testing, and the comparability of NPT results with central laboratory results
should be established. If none available an alternative system of verification should be
considered.
NPT should be subject to on-going monitoring to verify accuracy and comparability of the results to
those of the central laboratory.
Recommendation 6. Develop standard operating procedures and protocols for all NPT.
Protocols should be developed and implemented for all NPT services. Standard operating procedures
(SOP) should be developed and implemented for all aspects of the NPT service, including the
performance of the test, record keeping, interpretation of results, patient referral criteria, expert
laboratory guidance, quality assurance, patient and staff health and safety.
Recommendation 7. Ensure that anyone performing NPT is trained and on-going competence is
assessed.

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It is imperative that all staff performing NPT receive documented training and are competent in the
use of the test. Records should be kept of staff who have been trained in carrying out and/or
interpreting test results.
- Implement a mandatory staff training and competency programme.
Recommendation 8. Implement a quality assurance programme, including internal quality control
and external quality assessment for all NPT.
Accreditation requires all laboratories and NPT users to have a rigorous quality management system
in place, including at a minimum internal quality control (IQC) and external quality assessment
(EQA). IQC must be performed on IVDs in accordance with the manufacturer’s instructions, to ensure
the accuracy of the test result generated. NPT providers must also participate in an appropriate EQA
scheme. In the event that a suitable NPT EQA scheme is not available commercially, an equivalent
arrangement must be developed with the local laboratory. Both IQC and EQA are key to assuring the
accuracy and reliability of a NPT service. The two procedures are complementary.
- IQC primarily monitors day to day reproducibility (precision) and detects systematic errors in
any one day’s procedures. IQC samples are commercially available with known
concentrations of analytes. Mean values are established for both normal and abnormal
levels by repeated estimations by the laboratory or NPT operational team. Patient samples
should only be run when controls are within the acceptable range.
- EQA aims to ensure that test results are reliable and comparable no matter where they are
performed. Participants in an EQA scheme test samples with unknown values and the
result(s) are returned to the EQA organiser. A report is then provided to participants that
compares the submitted result with a target value. The participant can also see how they
compare to other sites. Analytical quality is determined by assessing the difference between
the result and the target value. There are national and international schemes available.
Recommendation 9. Ensure patient results are reviewed and interpreted by appropriately
qualified persons.
Patient results should only be reviewed or interpreted by appropriately trained personnel whose
identity should be recorded in all cases.
Appropriate referral criteria should be in place which may include referral to a local hospital or GP.
Confirmatory laboratory testing is also required for some conditions such as diabetes mellitus where
NPT is not considered acceptable for diagnosis8-9
.
A procedure for communication of critical NPT results should be in place. For many tests, grossly
abnormal or clinically unexpected NPT values require confirmatory testing using a laboratory
method. Appropriate referral criteria should be in place to ensure that confirmatory testing is
performed and patients are referred for further medical attention as necessary.

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All patient and quality control results should be recorded appropriately either via paper or electronic
format in accordance with defined procedures and the General Data Protection Regulations
(GDPR)10
. This should also include specific test batch numbers as appropriate, the date and time of
analysis and operator identification. Patient results must be recorded in the patient’s health record.
Recommendation 10. Ensure full traceability of all IVDs used (including reagents and
consumables).
NPT should be reviewed and monitored on an on-going basis and a test should be withdrawn or
suspended in the event of a safety corrective action, for example, a recall.
Unique Device Identification (UDI) is a system used to identify and facilitate traceability and incident
reporting of IVDs within the healthcare supply chain. Under the IVDR, manufacturers shall assign and
maintain unique UDIs for their IVDs.
- There should be full traceability of all NPT IVDs, reagents and consumables used to facilitate
incident reporting and to ensure appropriate action is taken in the event of a Field Safety
Corrective Action (for example a recall or other market action for safety reasons).
- Recording of specific batch numbers is important in the event of a recall by the manufacturer or
other market action for safety reasons.
- A system to review and take action on Field Safety Notices (FSNs) issued by IVD manufacturers
should be in place.
- In addition, systems should be in place to review and take action where appropriate on safety
notice / information notices and any other communications issued by the HPRA and any other
relevant bodies.
Recommendation 11. Ensure health and safety and waste management training for staff using
NPT.
Appropriate health and safety training and waste management training should be provided to staff
performing NPT.
The organisation must provide appropriate facilities, premises, and NPT service delivery areas which
are fit for purpose and comply with relevant health and safety legislation, building and fire
regulations.
A procedure must be in place for the safe disposal of biological waste and/or sharps in accordance
with the appropriate health and safety and/or infection control legislation.
Recommendation 12. Ensure all IVDs meet national and European IVD legislative requirements.

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NPT devices must be CE marked as this is an indication that the device meets the requirements of
the relevant legislation.
- Only IVDs that are approved by the NPT steering group should be used for NPT. This
requirement should apply to all IVDs irrespective of whether they have been purchased, loaned,
gifted or leased to the organisation.
Recommendation 13. Report adverse incidents to the designated committee, the manufacturer
and the HPRA.
All adverse incidents that occur with NPT devices must be reported to the designated hospital
committee, and should be reported to the manufacturer, the HPRA, and the appropriate regulatory
body if necessary. The HPRA website has an online tool and a downloadable form to facilitate
reporting of adverse incidents.
Recommendation 14. Include all NPT results in the patient’s health record, ideally by
implementing ICT connectivity.
Patient results must be recorded in the patient’s health record.
NPT IVDs should be password-protected and only accessible by certified users11
. Breeches of ICT
governance including password sharing precludes effective audit and is a risk to quality and patient
safety.
Connectivity allows central recording of patient results and quality parameters and should be
resourced to a level which avails of the latest technology including password-protection of analysers,
integration of results with the patient’s electronic healthcare record, operator identification, and
unique patient identification.
Connectivity also facilitates remote monitoring of NPT analysers from a hub in the local laboratory or
manufacturer for on-going analytical performance, fault diagnosis, preventative maintenance, and
trouble-shooting in the event of problems.
1.7 Conclusion
The implementation of the recommendations in this guideline, which replaces the two previous Irish
guidelines12-13,
should facilitate a well-managed and appropriately governed system for the provision
of NPT services which, if properly used, will deliver considerable benefits to the Irish health service
and will minimise risks for patients.

19
1.8 Chapter references
1. In-Vitro Diagnostic Medical Device Regulation 2017/746/EU. HPRA website. Accessed
14/4/2021.
2. I.S. EN ISO 15189:2016 (Medical Laboratories - Requirements for quality and competence).
NSAI website (purchase required). Accessed 14/4/2021.
3. I.S. EN ISO 22870:2016. Point-of-care testing (POCT) - Requirements for quality and
competence. NSAI website (purchase required). Accessed 14/4/2021.
4. European Tissues & Cell Directive 2004/23/EU. Accessed 14/4/2021.
5. Regulation (EC) No 765/2008. EUR-Lex (Access to European law). Accessed 14/4/2021.
6. Irish National Accreditation Board. Policy for accreditation of point of care testing (PS31).
INAB website. Accessed 14/4/2021
7. Guidance on the Provision of Testing Services in Pharmacies. Pharmaceutical Society of
Ireland, Version 3, October 2019. PSI website. Accessed 14/4/2021.
8. Definition, Diagnosis and Classification of Diabetes Mellitus and its Complications. Report of
a WHO Consultation. World Health Organisation, 1999. Accessed 14/4/2021.
9. Sacks DB, et al. Guidelines and recommendations for laboratory analysis in the diagnosis and
management of diabetes mellitus. Diabetes Care 34(6): e61-99, 2011. Accessed 14/4/2021
10. General Data Protection Regulation: Information on EU data protection rules and GDPR
download (as gaeilge), European Commission. Accessed 14/4/2021.
11. HSE Password Standards Policy. HSE website. Accessed 15/4/2021.
12. Guidelines for Safe and Effective Management and Use of Near Patient Testing in Primary
and Community Care, 2008. HPRA website. Accessed 14/4/2021.
13. Guidelines for Safe and Effective Management and Use of Point of Care Testing, 2007. HPRA
website. Accessed 14/4/2021.

20
Chapter 2
Definition, uses and risk/benefit analysis for
NPT
This chapter defines NPT and gives an overview of the current uses for NPT as well as a risk/benefit
analysis.
2.1 Definition of NPT
A device for NPT has recently been defined under the IVDR1
(Article 2) as any device that is not
intended for self-testing but is intended to perform testing outside a laboratory environment,
generally near to, or at the side of, the patient by a health professional. Accordingly, any NPT device
operated by any health professional and used in either hospital or primary care/community settings
is included.
Devices that are used by patients or other individuals for self-testing are not covered by the term
NPT and are outside the scope of this guideline.
Pending implementation of the new IVDR in 2022, all IVDs used for NPT are currently regulated
under the IVD Directive 98/79/EC2
. The HPRA is designated as the competent authority for medical
devices and IVDs in Ireland. Its role is to ensure that all IVDs placed on the Irish market comply with
the essential requirements of the IVD Directive and related national legislation.
There is a statutory obligation on manufacturers to notify the HPRA of all adverse incidents involving
IVDs. Direct user reporting to the HPRA, although not mandatory, is strongly encouraged. There is
also a requirement to report to risk management groups in accordance with the local organisation’s
policy.
2.2 Existing and emerging uses for NPT
NPT remains mostly confined to the hospital setting. However, the range of NPT tests in the hospital
sector has broadened and the volume of tests performed is now very large. It is now commonplace
for blood gas analysers, glucose-measuring devices (glucometers), blood ketones, pregnancy testing,
coagulometry, drugs of abuse and occult blood to be widespread throughout hospitals. Maternity
specific testing such as with fibronectin has been implemented.
Microbial testing by NPT is also on the increase generally, including for SARS-CoV-2. Interim guidances
concerning the advantages and drawbacks of the various types of NPT IVDs currently available for
SARS-CoV-2 applications have been issued by the HSE3
, NPHET4
, the HPSC5
, and the WHO6
. Rapid
health technology assessments have also been conducted by HIQA7
.
NPT devices produce a rapid test result in the immediate vicinity of the patient often in areas such as
the emergency department, intensive care unit or other designated areas of the hospital. The
rapidity of obtaining a result can increase clinical effectiveness and contribute to improved

21
outcomes for patients, but it is imperative that the result provided by the device is accurate, reliable
and visible in the patient’s health record.
NPT IVDs currently available on the market encompass all laboratory medicine disciplines. Table 2.1
provides examples of NPT currently in use in a hospital setting. The types of samples used for NPT
include whole blood, urine, serum, stool and saliva.
TABLE 2.1
Examples of applications available on NPT devices in a hospital setting
Blood gases, co-oximetry, electrolytes, lactate, renal function, haemoglobin
Cardiac biomarkers, renal markers, bilirubin, creatinine, ionized magnesium, procalcitonin
Cholesterol, triglyceride and high-density lipoprotein cholesterol (HDL-C)
Blood glucose
Blood ketone
Haemoglobin A1c
Alcohol and toxicology (paracetamol, drugs of abuse)
Intra-operative PTH measurement
Urinalysis (with or without a reader)
Urine albumin and albumin/creatinine ratio
Placental alpha microglobulin-1 (PAMG-1)
Detection of pregnancy and ovulation
Stool occult blood
Fibronectin
Anticoagulant therapy monitoring – INR
Activated clotting time
D-dimer
Thromboelastometry
Full blood count
Infections (chlamydia, human immunodeficiency virus, hepatitis B, Hepatitis C, influenza virus)
SARS-CoV-2
The improved reliability and range of NPT devices is leading to an increased use in community clinics
and GP surgeries. Table 2.2 provides examples of NPT currently in use in a community setting.
TABLE 2.2
Examples of applications available on NPT devices in a community setting
Blood glucose
Haemoglobin A1c
Cholesterol, triglyceride and high-density lipoprotein cholesterol (HDL-C)
Detection of pregnancy and ovulation
Urinalysis (with or without a reader)
Stool occult blood
Anticoagulant therapy monitoring

22
Infections (chlamydia, human immunodeficiency virus)
SARS-CoV-2
2.3 Risks and benefits of NPT and the need for confirmatory testing
When a healthcare professional undertakes a pathology test adjacent to the patient rather than
sending samples to a central laboratory, there is an expectation that the faster result turnaround will
improve patient care. However, a faster result is only better when it is an accurate result i.e. no pre –
analytical errors, equipment fit for purpose and operated by a fully trained and competent operator.
This document provides guidance for safe and effective NPT, using IVDs that are fit for purpose and
delivered by a competent individual for appropriate patients, producing quality results which
become part of the patient record.
The major risks to the delivery of safe and effective NPT arise from:
 poor operator training and lack of competency assessment
 lack of appropriate supervision, governance and accreditation of the NPT service
 failure to use internal quality control and/or external quality assessment schemes
 inappropriate testing by inexperienced personnel
 uncertainty on how to act on results
Advances in technology and legislative control have also resulted in more reliable instrumentation.
However, users need to be aware that NPT is rarely a replacement for the conventional laboratory
services, but rather a supplement to it.
In situations where critical clinical decisions are made on NPT results and where out-of-range results
are obtained, confirmatory testing by the central laboratory may be required by the local NPT policy.
Though analytical results are provided more rapidly with NPT there are concerns about the reliability
of results obtained by non-laboratory personnel.
Incorrectly performed testing or inappropriately interpreted results can put patients at risk. In some
situations, it may be more appropriate to have analyses performed in a clinical laboratory. The
provision of NPT should not be considered when the laboratory can provide the result in a timely
manner, appropriate to the clinical condition.
2.4 Unnecessary testing and financial risks
There are financial risks associated with excessive or unnecessary NPT. The cost per test of NPT
generally exceeds that of the clinical laboratory so inappropriate or excessive testing can
significantly increase expenditure.
Staff costs for NPT can be substantial but are rarely identified as such in hospital budgets. Higher
NPT costs may however be offset by more efficient use of resources in other areas of healthcare

23
delivery. A comprehensive cost benefit analysis addressing these matters should be undertaken
before deciding to implement a new NPT service.
1. In-Vitro Diagnostic Medical Device Regulation 2017/746/EU. HPRA website. Accessed
14/4/2021
2. Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in
vitro diagnostic medical devices. Accessed 14/4/2021
3. Antigen testing for COVID-19. HSE website. Accessed 14/4/2021
4. National Public Health Emergency Team Subgroup - Diagnostic Testing Approaches: A
Strategic Framework. Department of Health, Irish Government website. Accessed
14/4/2021.
5. Interim guidance on use of Antigen Detection Tests in the public health system in Ireland.
HPSC website. Accessed 14/4/2021
6. Advice on the use of point-of-care immunodiagnostic tests for COVID-19. WHO website.
Accessed 14/4/2021
7. Health Information and Quality Authority. COVID -19 evidence synthesis publications. HIQA
website. Accessed 14/4/2021

24
Chapter 3
Governance and management of NPT
services: the role of the NPT steering group
Clinical governance is a systematic approach to maintaining and improving the quality of patient care
and controlling clinical risk. It is an essential part of any NPT service and is best delivered by
establishing a multidisciplinary NPT steering group. The overall approach and inter-relationship
between NPT steering group and other stakeholders is summarised in Figure 1 which applies to all
healthcare sectors considering NPT.
Figure 1. Clinical governance schema for NPT
3.1 Responsibility for NPT services
The primary purpose of the NPT service is to facilitate timely, evidence-based decision making in the
diagnosis and treatment of patients by ensuring the delivery of safe, effective, quality-oriented tests
at or near to the patient’s bedside.
The NPT steering group will be accountable for the delivery of all NPT services. The chairperson of
this group will usually be a laboratory consultant. Laboratory consultants from participating
disciplines will provide direction for their particular NPT service. A person with overall responsibility
for co-ordination must be designated for each NPT service, whether existing or proposed. This will
usually be a senior laboratory scientist from the appropriate pathology discipline and will be a
member of the NPT steering group.

25
The NPT steering group should be accountable to the organisation’s executive management team,
whether in the hospital sector or a primary or community care organisation. A formal link with the
local pathology directorate is desirable. A template for the NPT steering group including terms of
reference can be found in Appendix 1.
Note that the existence of this governance structure does not negate the responsibility of the
individual analyst to work in a competent manner. The onus is on the nurse manager or head of
department of each unit utilising NPT to ensure that all authorised operators have been trained and
have demonstrated competence. The individual conducting the analysis is accountable for
maintaining their competence and for the results they generate using NPT devices.
Recommendation 1: Establish an NPT steering group and organisation-wide NPT policy.
3.2 Terms of reference of the NPT steering group
The NPT steering group should have the objectives set out in Table 3.1.
TABLE 3.1
Objectives of the NPT Steering Group
1. Ensure safe delivery of NPT for patients.
2. Provide clinical governance for NPT services through the development and
implementation of an organisation-wide NPT policy.
3. Establish NPT operational team(s) to oversee the day-to-day running of individual NPT
services.
4. Advise the organisation’s executive management team on all aspects of NPT, including
risk, benefits, resources required, new proposals and present and future strategy.
The NPT steering group needs to document its system for clinical and managerial governance in an
NPT policy, including a person designated as responsible and accountable for the service. This should
also ensure the organisation is compliant with relevant legislation, regulations, and accreditation
standards governing the use of NPT services, i.e.
 relevant European and National legislation,
 laboratory accreditation standards (EN ISO 15189 and EN ISO 22870),
 HSE requirements, e.g. medical records,
 risk management requirements,
 infection control and prevention requirements,
 data protection regulations.
3.3 NPT steering group membership
The minimum recommended membership is shown in Table 3.2.

26
TABLE 3.2
Minimum membership of the NPT Steering Group
A laboratory consultant from participating pathology disciplines.
NPT manager.
A senior management representative.
A senior scientist from participating pathology disciplines.
The manager of each or all NPT operational teams.
Clinical risk manager.
Senior medical representatives from participating services.
Senior nursing representatives from participating services.
IT representative.
Risk manager.
Financial advisor.
Additional members may be included or co-opted (e.g. pharmacy, supplies, clinical engineering,
infection control) depending on the needs of the local service.
3.4 Responsibilities of the NPT steering group
The range of responsibilities of the NPT steering group are given in Table 3.3. Whereas the steering
group must have competence and provide oversight in all of these areas, the day-to-day operational
aspects may be delegated to an NPT operational team for implementation (see Chapter 5).
TABLE 3.3
Responsibilities of the NPT steering group
1. To evaluate and approve all NPT services within the organisation against the
recommendations in this guideline (including new NPT proposals and existing “legacy”
NPT services), regardless of whether the NPT IVDs concerned are new, gifted, loaned, or
existing.
2. Both new NPT service proposals and existing NPT services should also be evaluated to
ensure that clinical need and effectiveness are defined and that there are auditable
quality objectives which can be monitored.
3. NPT services which are substandard or ineffective should either be rejected or, where
appropriate, recommendations can be made to achieve the required standard.
4. To review and monitor quality objectives as required and have the authority to withdraw
and/or suspend service in the event of a safety-related or performance issue or lack of
clinical effectiveness.
5. To ensure that only approved CE marked IVDs suitable for their intended use are used for
NPT.

27
TABLE 3.3
Responsibilities of the NPT steering group
6. To ensure that IVDs are procured and commissioned in an appropriate manner and
according to the organisation’s policies.
7. To establish a register of all approved NPT sites along with an asset register of all IVDs,
consumables and reagents used at these sites within the organisation, which can also
facilitate incident reporting and device traceability for example in the event of a Field
Safety Corrective Action (FSCA)
8. To ensure that NPT devices fulfil the requirements of National and European legislation,
laboratory and hospital accreditation standards (for example: JCI, ISO) and other relevant
standards.
9. To comply with HSE requirements in relation to data protection, patient confidentiality,
risk management and procurement.
10. To ensure that there is a procedure to document all patient results appropriately and to
transfer them to the permanent healthcare record. Results should be traceable to the
location where the analysis is performed, and the operator reporting the analysis.
11. To ensure an effective system for clinical review of results, including communication of
critical results and confirmatory testing.
12. To monitor and review patient-safety related incidents, including adverse incident
reporting and review of safety/information notices issued by manufacturers and the
HPRA.
13. To ensure that the NPT IVDs are operated only by trained and competent users using
password protected access.
14. To define criteria for taking action against unsatisfactory operator performance,
inappropriate use and poor quality assurance practices and for withdrawal of the IVD
where appropriate.
15. To review overall NPT performance and trends identified through audit and quality
assurance.
16. To ensure that there is adequate support and appropriate use of resources for NPT.
17. To support the NPT manager(s) and operational team(s).
18. Traceability. To advise the organisation regarding the need to recall/withdraw an IVD in
the event of a safety or performance issue until appropriate remedial action is taken, such
as a field safety corrective action.
More information on the role of NPT operational groups is provided in Chapter 5.

28
Traceability (see also Chapter 5) is an important role for the NPT steering group who will need to be
in a position to advise the organisation of any actions needed in the event of a recall or patient
safety-related issue involving an NPT IVD.
3.5 Governance issues and the IVD industry
It is strongly advised that IVD industry representatives present proposals initially to the NPT steering
group preferably through the chairman, or through the NPT manager, instead of approaching
individual end users directly.
It will be the responsibility of the individual contacted to inform the relevant specialties concerned.
No NPT device must be put in place without the prior approval of the NPT steering group.
The IVD industry has a role in supporting the operational team with commissioning, operator
training, development of documentation, auditing and on-going operation of NPT services and
equipment.
3.6 Primary care
GPs should be aware of the expertise in NPT available from the local hospital laboratory service and
should make use of this by obtaining advice before commissioning any NPT in their practices. The
local hospital laboratory should provide support and quality assurance monitoring and should be
willing to do this, resources permitting. Regional integrated care organisations (RICOs) and other
primary and community care organisations should also avail of the expertise of the local hospital
laboratory.
3.7 Community pharmacists
Community pharmacists should avail of the expertise in NPT available from the local hospital
laboratory service and should make use of this by obtaining advice before commissioning any NPT in
their practices. The local hospital laboratory should provide support and quality assurance
monitoring and should be willing to do this, resources permitting.
Community pharmacists should be aware of the governance issues set out in this document and
their universal applicability as well as the latest version of the Guidance on the Provision of Testing
Services in Pharmacies issued by the Pharmaceutical Society of Ireland1
.
NPT should form part of a collaborative network of care with other relevant healthcare providers.
The same quality standards should apply in pharmacies as elsewhere. Hence, pharmacists should
give consideration to discussing their plans with the local pathology service and GPs.
Particular attention should be given to the use of clinically and analytically validated assays,
recognised units of measurement, standardised methods and comparability of results with the local
laboratory.
1. Guidance on the Provision of Testing Services in Pharmacies. Pharmaceutical Society of
Ireland, Version 3, October 2019. PSI website. Accessed 14/4/2021

29
Chapter 4
Commissioning NPT services
NPT services (both new proposals and existing services) should only be introduced in consultation
with the NPT steering group and have the approval of the laboratory consultant from the
appropriate discipline.
Recommendation 2. Consult with local laboratory.
4.1 Case of need and business case
All new proposals must be justified by a case of need and supported by a full business case. The
commissioning process up to the point of receiving approval from the NPT steering group is
illustrated in Figure 2.
Recommendation 3. Document the case of need involving all stakeholders.
Figure 2. NPT commissioning process up to approval by NPT steering group
Appendix 2 contains an application form suitable for new NPT proposals which is intended to be
completed by the end-user proposing the new NPT service, however with assistance for the more
technical aspects from the laboratory. The finance department of the organisation should also assist
with the business case development. Appendix 3 contains a template to help with cost-benefit
analysis.

30
The case of need/application from should include an assessment of all options available to deliver
the required pathology service, including the costs of all staff involved, training, external quality
assessment schemes, equipment, reagents used, servicing and repairs. A specification of
requirements (suitable for tender) and a scheduled implementation plan should be presented. It is
acknowledged that increased costs associated with NPT may be offset by clinical benefits and/or
cost savings achieved elsewhere in the organisation. It is also the case that improvements in
turnaround time to the central laboratory frequently obviate the need for NPT.
4.2 Resources
It is important to recognise that adequate resources are required for the implementation and on-
going support of NPT. A NPT manager is key to the overall operation. Link nurses are also required at
ward level and a training coordinator is recommended for large organisations. Depending on the
complexity and scope of NPT services, it is envisaged that the NPT management team would require
dedicated staff of at least 2 whole time equivalents. These staff would often be a laboratory trained
senior or specialist scientist. Ideally staff numbers should include cover for leave. The grade of chief
medical scientist should be considered for very large services. A further 1 whole time equivalent
designated training specialist (preferably with clinical experience i.e. nurse / pharmacist /
radiographer /advanced practitioner) would also be required to coordinate the day-to day operation
of NPT at ward or clinic level.
Figure 3 provides an overview of the various ongoing tasks that arise once a new NPT service has
been commissioned and the equipment supplied. An integrated quality management system which
includes the users is of course central to this, with documentation and follow-up of errors and non-
conformances. Evidence1
suggests these are more likely to occur during test analysis than in the case
of a test carried out in the central laboratory, emphasising the need for close teamwork with users.

31
Figure 3. Various tasks involved post-approval of a new NPT service (SOP= standard operating procedure; QRG = quick
reference guide; EQA = external quality assessment; IQC = internal quality control)
4.3 Space
Space available must be adequate to accommodate the equipment, consumables and
documentation. The location must minimise risks to the health and safety of staff and patients. It
should have sufficient electrical sockets and network points or Wi-Fi coverage for the equipment.
The environment should be controlled to comply with legislation and manufacturers’
recommendations. A dedicated refrigerator and possibly a freezer for reagent storage should be
available, if required, with temperature monitoring capability. A safe sturdy area to locate a
centrifuge may also be required if serum separation is necessary. Equipment should be arranged to
allow for operation in a manner that supports high quality work, internal quality control, external
quality assessment, result documentation and maintenance. Provision must be made for safe
disposal of sharps, clinical and non-clinical waste, and confidential information. Space requirements
will vary for particular tests or groups of tests but should be defined by the laboratory discipline.
1. O’Kane MJ, McManus P, McGowan N, Lynch PLM. Quality Error Rates in Point-of-Care
Testing. Clinical Chemistry 2011; 57(9): 1267–1271. Accessed 14/4/2021

32
Chapter 5
Implementing NPT services
This chapter details the implementation for NPT in all settings that would be usual in order to
achieve full ISO 15189/22870 accreditation (see also appendix 4 for a checklist). The NPT operational
teams are responsible for implementing NPT services. All NPT services should be documented in
appropriate standard operating procedures, which should be approved by the NPT steering group.
5.1 NPT operational teams
One or more NPT operational teams may be appointed by the NPT steering group to oversee the
day-to-day operation of NPT services. One or more NPT managers may lead the teams.
The developmental phase of establishing operational teams may be led by a senior scientist, who
may, in the established phase of NPT, hand it over to a specifically appointed laboratory scientist as
NPT manager.
Recommendation 4. Establish an NPT operational team.
5.2 The role of the NPT operational team
The role of the teams is described in Table 5.1.
TABLE 5.1
Role of the NPT operational teams
1. To develop standard operating procedures for pre-analytical, analytical and post-
analytical processes for each NPT device.
2. To develop a system for training, competence assessment, certification and registration of
operators which includes maintaining a register of certified trained users and provision of
secure operator identity codes for the NPT service access.
3. To implement and monitor quality assurance programmes, both internal and external
(where available), for the IVD and review on-going performance using a quality
management system.
4. To validate and compare the NPT method with the current laboratory method and
provide comparative data for review by the NPT steering group.
5. To ensure that audits are conducted and appropriate corrective action is implemented
where necessary.

33
TABLE 5.1
Role of the NPT operational teams
6. To ensure that the adverse incident reporting policy is adhered to and that non-
conformance reports are completed and reviewed.
7. To establish a procedure for service and maintenance of IVDs in accordance with
manufacturers’ instructions.
8. To maintain a system to support Field Safety Corrective Actions (FSCA) - market actions
undertaken by a manufacturer for safety reasons. For example, a recall or withdrawal of
an IVD or its associated reagents and consumables.
9. To advise the NPT steering group on appropriate actions (e.g. whether to
withdraw/quarantine NPT IVDs) due to a safety or performance issue, until appropriate
remedial action is taken, such as a Field Safety Corrective Action (FSCA) by a
manufacturer.
5.3 Validation and verification of NPT IVDs
Recommendation 5. Ensure all IVDs are CE marked, adequately validated and independently
verified.
It is essential that all NPT IVDs carry a CE mark – this marking is described further in Chapter 6
(Regulatory requirements). ISO 15189 also requires that test procedures are adequately validated
and undergo verification by the laboratory (independently of the manufacturer) before being
introduced to provide objective evidence that the IVD is fit for purpose.
 Test methods are verified under conditions of normal use by use of blank samples, control
samples, duplicate samples, calibration checks, IQC monitoring and EQA performance.
 Aspects of verification should include sensitivity and specificity, accuracy and precision,
repeatability, reproducibility, limits of detection, limit of quantitation.
 Uncertainty of measurement should be established for each NPT method
 Where possible, a backup laboratory method should be available for any NPT to provide
confirmatory testing, and the comparability of NPT results with central laboratory results should
be established.
NPT should undergo on-going verification of IVD results and on-going monitoring to ensure
continued accuracy and comparability of the results to those of the central laboratory.
A QMS should ensure there is on-going verification of IVD results.

34
5.4 Develop standard operating procedures for NPT
Recommendation 6. Develop standard operating procedures and protocols for all NPT.
Protocols should be developed and implemented for all NPT services. Written operational
procedures (including quick reference guides) must be available for all point of care analyses. These
procedures must include instructions on the operation and maintenance of the equipment, internal
quality control procedures, safe working practice and identified risks, the interpretation of error
messages and the recording of results. Procedures should clearly identify mechanisms for
communication of failures and spurious results to the NPT operational team. These operational
procedures should be controlled documents and should be linked to the laboratory or other quality
management systems.
5.5 Training
Recommendation 7. Ensure that anyone performing NPT is trained and demonstrates on-going
competence.
All staff involved in NPT must be trained and competent in the use of the IVD (see Appendix 8 for a
training record template). The training and certification of NPT users should be overseen and
monitored by the NPT operational team.
Training may be provided by the NPT operational team directly, by dedicated staff members as part
of a cascade trainer programme under guidance of the NPT operational team and /or the
manufacturer or manufacturer’s representative again under guidance of the NPT operational team.
All trainers should undergo witness audits to ensure conformity of training for all devices. Many of
the vendors have established training programmes. Externally provided training tools such as
presentations and documentation should be reviewed, modified to suit local needs and approved by
the local NPT operational team.
Advantage could be taken of e-learning programmes.
Only staff whose training and competence has been established and recorded should be permitted
to perform NPT and access to the equipment must be restricted to these staff. It is the responsibility
of all users of NPT devices to attend the training sessions provided and to attain and maintain
competence on the relevant NPT devices at intervals as defined by the NPT operational team.
The topics described in Table 5.2 should be included in the staff-training programme for NPT.

35
TABLE 5.2
Components of a NPT staff training programme
Instructions on safe working practices.
Principles of operation of the IVD including daily maintenance requirements
Action on improper and unsafe use of a NPT IVD.
Review of the manufacturer’s instructions for use, basic principles of the analysis, limitations of
the IVD, interferences including drugs and antibodies, unsuitability for use scenarios (e.g. patient
perfusion, surgical intervention).
Review and understanding of error messages, interpretation and appropriate responses.
Calibration and internal quality control requirements, to include performance, appropriate record
keeping and required actions for failed results.
Patient preparation, sample collection and handling according to health and safety regulations
and the manufacturer’s stated requirements and the effects of pre-analytical interferences
including site preparation, pre-existing infusions, air bubbles and time from draw analysis.
Recording of patient results, interpretation of results, appropriate responses to critical results,
confirmatory testing procedures, contacting the NPT operational team, and obtaining clinical
advice for out-of-range and spurious results.
Facilitating the assignment of operator identification numbers to trained certified NPT users
Inclusion in the register of certified trained users and notification of the programme for retraining
and monitoring.
Inventory management for NPT IVDs and their associated reagents and consumables and all
operators including retraining intervals and ongoing competency assessment processes
Procedure for recording of adverse incidents with IVDs including documentation, investigation,
reporting to the NPT operational team, NPT steering group, and manufacturer where required.
Procedures for receiving and actioning Safety and Information Notices from the HPRA and Field
Safety Notices (FSNs) from manufacturers.
Procedures for recording of non-conformance and change control forms and recall/traceability of
IVDs and their associated reagents and consumables when required.
ICT connectivity and its availability
Many of the vendors have established training programmes, which must be reviewed and modified
to suit local needs. Advantage could be taken of e-learning programmes.

36
5.6 Competence/proficiency testing of NPT operators
The NPT operational team should assess the competence of new NPT operators and should
periodically re-assess existing NPT operators. This may be done by observing an operator carrying
out an actual test and assessing performance against the SOP. Deviations observed in technique
from that specified in the SOP should be corrected immediately, in which case the operator can be
re-certified as competent. Defects in theoretical knowledge should be addressed by appropriate
educational sessions.
The advantage of this approach is that all aspects of actual NPT practice can be observed, assessed
and corrected (e.g. pre- analytical considerations, specimen collection, analysis, interpretation of
results and further action). The assessment should be conducted as a peer-based practice
improvement measure rather than an examination.
Competence/proficiency testing is supplemental to the standard laboratory quality assurance
measures. Ideally, all NPT operators should be assessed and re-certified annually, or more frequently
where usage of NPT is low.
5.7 Quality assurance programme
Recommendation 8. Implement a quality assurance programme, including internal quality control
and external quality assessment for all NPT.
Quality assurance is an integral component of any NPT service and includes all the measures taken
to ensure the reliability and accuracy of the patient result. It is important that all NPT IVDs are
included in a quality assurance programme and that this is operational prior to patient testing at
each site. The quality assurance programme should be overseen and monitored by the NPT
operational team and appropriate action should be taken if adherence to quality standards is not
maintained. The role of the laboratory is integral to the implementation and management of the
analytical quality assurance for NPT. Table 6.2 illustrates the elements which should be considered.
TABLE 5.3
Elements of quality assurance
Performance and documentation of appropriate internal quality control and / or calibration.
Correct patient identification.
Selection of the appropriate test.
Obtaining a satisfactory sample and sample integrity.
Performance of the test in accordance with the manufacturer’s instruction.
Correct interpretation of the result and appropriate action taken.
Recording of the test result in the patient record.

37
5.8 Internal quality control
IQC is a means of determining that the IVD is performing correctly at that specific time and that the
patient result is likely to be reliable before it is released and acted on.
The SOP for each IVD should outline the material to be used, specify the frequency at which the IQC
is performed and define the acceptable limits for the IQC material prior to testing a patient sample.
All NPT users should be educated as to the importance of the IQC procedures, appropriate action to
take in the event of failed quality control, and the implications when quality control is not performed
according to the stated protocol.
It should be noted there are two main types of IQC – electronic and liquid. An effective quality
management system requires correct use of both types.
5.9 External quality assessment
EQA is a means of determining how a particular IVD is performing in comparison to similar IVDs at
different sites and to other manufacturers IVDs or other laboratory analysers.
The EQA material is a sample of an unknown value, which may be provided by an external quality
assessment scheme such as the Irish External Quality Assessment Scheme (IEQAS), other
international schemes, or alternatively prepared by the laboratory or manufacturer for provision to
all NPT sites within the organisation. The laboratory should be responsible for the implementation
and management of the EQA and provide feedback to the NPT operational team.
Quality assurance performance should be reviewed under the governance of a quality management
system.
5.10 Recording of results and audit trail
All patient results must be recorded in the patient’s permanent record. The date and time of
analysis, NPT operator identity, reagent lot/batch number and the UDI should be included with the
patient result to allow full traceability for NPT. A permanent record of all quality control data should
be maintained.
5.11 Reviewing results
Recommendation 9. Ensure patient results are reviewed and interpreted by appropriately
qualified persons.
Patient results should only be interpreted and reviewed by appropriately trained personnel and the
operator identity should be recorded in all cases. A procedure for communication of critical NPT
results should be in place. Grossly abnormal NPT values or values inconsistent with the patient
clinical history may require confirmatory testing using a laboratory method. Confirmatory laboratory
testing is also required for some conditions where NPT is not acceptable for diagnosis, such as
diabetes mellitus1-2
.

38
Appropriate patient referral criteria should be in place, which may include referral to a local hospital
or GP.
5.12 Traceability and recall
Traceability and recall of NPT IVDs including any reagents and consumables used must be possible in
any NPT implementation. The NPT steering group will need to be in a position to advise the
organisation of any actions needed in the event of a recall or patient safety-related issue involving
an NPT IVD.
Recommendation 10. Ensure full traceability of all IVDs used (including reagents and
consumables).
In turn, the NPT operational teams will need to establish and maintain a system to support
traceability, for example in the event of a recall, and which will usually be linked to the
organisation’s asset register.
NPT should be reviewed and monitored on an on-going basis and a test should be withdrawn or
suspended in the event of a safety related issue e.g. a recall.
Unique device identification (UDI) is a system used to identify and facilitate traceability of
IVDs within the healthcare supply chain. The UDI is a series of numeric or alphanumeric characters
created through internationally accepted device identification and coding standards and allows
unambiguous identification of specific IVDs on the market. Under the IVDR, manufacturers shall
assign and maintain unique UDIs for their IVDs.
The introduction of UDI under the IVDR should lead to improved incident reporting, targeted field
safety corrective actions (FSCAs) and better monitoring by competent authorities.
It should also help to reduce medical errors and to fight against falsified IVDs. Use of the UDI system
should also improve purchasing and waste disposal policies and stock-management by health
institutions and other economic operators and, where possible, be compatible with other
authentication systems already in place in those settings.
 There should be full traceability of all NPT IVDs, reagents and consumables used to ensure
appropriate action can be taken in the event of a recall.
 Recording of specific batch numbers is important in the event of a recall by the
manufacturer or other market action for safety reasons.
 A system to review and take action on FSNs issued by NPT IVD manufacturers should be in
place.
 In addition, systems should be in place to review and take action where appropriate on
safety notice / information notices and any other communications issued by the HPRA and
any other relevant bodies.
5.13 Maintenance and service

39
A maintenance and incident logbook (paper or electronic) should be maintained for each NPT device
to record details of maintenance, faults, repairs and corrective action. The NPT operational team
should nominate an individual who is responsible for responding to issues logged and recording the
corrective actions taken in this logbook.
The preventative maintenance and servicing of NPT devices is essential to ensure a functional and
reliable NPT service within the organisation. It is important therefore that the NPT operational team
identifies persons to be responsible for the day-to-day care of an IVD for each NPT site and that this
is communicated to users. Responsibility for other maintenance should be clearly identified by the
NPT operational team and could be the device’s manufacturer/supplier, the clinical engineering staff
and/or appropriate laboratory staff. All such maintenance and servicing should be conducted in
accordance with the manufacturer’s instructions.
A service contract with the NPT device supplier to ensure engineering support and supply of
consumables is essential.
It is recommended that a register, based on the organisations asset register for all IVDS used at NPT,
be used to update the maintenance and servicing records for these devices, as appropriate.
The day-to-day maintenance of a NPT device may include some of the following elements:
 ensure that the device is kept clean and in good and safe working order
 ensure good stock control of all reagents, consumables, calibrators and controls within their
shelf-life
 temporarily withdraw any device from the NPT service that is not performing to the
manufacturer’s specification and ensure that it is not used again until the appropriate
remedial action has been taken and the NPT steering group has been informed
 suspend/withdraw any NPT service in the event of a safety issue as directed by the NPT
operational team
5.14 Retention of records
Records of instrument maintenance, faults and corrective action, training records, quality control
records and medical records should all be retained for the length of time specified in the HSE’s Code
of Practice for Healthcare Records Management3
.
5.15 Health and safety
Recommendation 11. Ensure health and safety, and waste management training for staff using
NPT.
A risk assessment of hazards associated with the NPT IVDs needs to be completed. Special attention
must be given to avoidance of contamination of devices and the surrounding environment and
disposal of waste including sharps. Protocols for decontamination of devices and their immediate
environment should be available. All testing must be carried out in accordance with health and
safety regulations.

40
 Appropriate health and safety training and waste management training should be provided
to staff performing NPT.
 The organisation must provide facilities, premises, and NPT service delivery areas which are
fit for purpose and comply with relevant health and safety legislation, building and fire
regulations.
 A procedure must be in place for the safe disposal of biological waste and/or sharps in
accordance with the appropriate health and safety and/or infection control legislation.
1. Definition, Diagnosis and Classification of Diabetes Mellitus and its Complications. Report of
a WHO Consultation. World Health Organisation, 1999. Accessed 14/4/2021.
management of diabetes mellitus. Diabetes Care 34(6): e61-99, 2011. Accessed 14/4/2021.
3. HSE standards for healthcare records management. HSE website. Accessed 14/4/2021.

41
Chapter 6
Regulatory requirements for NPT: the role of
the HPRA
6.1 The IVD Directive 98/79/EC and the IVD Regulation 2017/746/EU
The majority of analytical devices (e.g. test kits and analysers) that are used for NPT fulfil the
definition of an IVD. Broadly, an IVD is a device intended by a manufacturer for the in-vitro
examination of specimens derived from the human body to provide information regarding a
physiological, pathological or therapeutic state.
All IVDs are currently regulated under the IVD Directive 98/79/EC and related Irish regulations. The
IVD Directive became mandatory in December 2003 and was implemented in Ireland via the
statutory instrument S.I. No. 304 of 2001, European Communities (In-vitro Diagnostic Medical
Devices) Regulations, 2001.
All IVDs available on the European market must meet the essential requirements in Annex I of the
IVD Directive and conformity to the directive is indicated by the presence of a CE mark on the device
labelling.
Recommendation 12. Ensure all IVDs meet national and European IVD legislative requirements.
NPT devices must be CE marked as this is an indication that the device meets the requirements of
the relevant legislation.
- Only IVDs that are approved by the NPT steering group should be used for NPT. This
requirement should apply to all IVDs irrespective of whether they have been purchased, loaned,
gifted or leased to the organisation.
The essential requirements of the IVD Directive aim to ensure that IVDs do not compromise the
health and safety of patients and users and are designed to achieve the performance specified by
the manufacturer for its intended purpose. This legislation introduces common regulatory
requirements dealing specifically with the safety, quality and performance of IVDs across Europe.

42
Figure 4. Representation of the CE mark that should be displayed on a medical device.
The HPRA is designated as the competent authority for medical devices in Ireland. Its primary role as
competent authority is to ensure that all IVDs placed on the Irish market comply with the medical
device legislation.
The regulatory system for IVDs has recently undergone substantial revision at European level. A new
European regulation on IVDs was published in May 2017 (Regulation 2017/746/EU), the IVD
Regulation (IVDR). This regulation will replace the existing IVD Directive and national SI and will be
fully applicable five years after entry into force (May 2022). This will bring about a number of
important changes to ensure safe access to new and innovative therapeutic and diagnostic devices
for patients. Some key changes include the classification rules for IVDs, conformity assessment
routes to be applied to demonstrate safety and performance and detailed requirements for
performance studies. A ‘device for near-patient testing’ is defined in Article 2 of the IVDR as “any
device that is not intended for self-testing but is intended to perform testing outside a laboratory
environment, generally near to, or at the side of, the patient by a health professional”. Of note
specific provisions are now made for near patient tests under the IVDR. It is important to note that
some of the provisions of the IVDR become applicable prior to 2022 and there are important
changes that manufacturers of NPTs should be aware of.
6.2 Risk assessment of IVDs used for NPT
An IVD is classified on the basis of the risk associated with the device and the relative dangers to the
public and/or a patient treatment/diagnosis by an IVD failing to perform as intended. The IVD
Directive requires manufacturers to perform a risk assessment for all devices. This risk assessment
should consider the use of an IVD in the NPT setting and any additional safeguards that should be
applied considering that the device is used outside the conventional laboratory setting and by
individuals who are not professionally trained in laboratory techniques.
The essential requirements in Annex I of the IVD Directive also specify the information to be supplied
by manufacturers with an IVD, to ensure it is used in a safe and proper manner. Paragraph 8.1 of this
annex states that the information should consider the training and knowledge of potential users.
Manufacturers should therefore ensure that this requirement is met for IVDs used as NPT, an
environment distinct from the laboratory setting.
6.3 Key changes with the new IVD Regulation
One of the key changes with the introduction of the IVD Regulation will be a move away from the list
based classification system currently in place under the IVD Directive. The regulation introduces a
new risk-based rule-based classification system.

43
Seven classification rules (Annex VIII Section 2) will divide IVDs into Class A (lowest-risk) to D
(highest-risk). Annex VIII Rule 4 states that devices intended for near patient testing will be classified
in their own right, thus they can be classified as Class A, B, C or D devices depending on the
associated risk. Application of the classification rules will be governed by the intended purpose and
inherent risk of the device (or the result generated by it). For example the detection of a
transmissible agent that causes a life-threatening disease (e.g. HIV) with a high or currently
undefined risk of propagation will be classified as Class D, whereas devices for testing blood glucose
will be classified as Class C. The level of regulatory oversight will be relative to the risk of the device.
For high risk devices, the notified body will request a reference laboratory to verify by laboratory
testing the claimed performance and compliance with the regulation.
The requirements for near-patient tests regarding performance, design and manufacture have been
strengthened under the IVDR to ensure they are appropriate for their intended use and in the
environment in which the device is intended to be used. Annex I, Chapter II, Section 19 specifically
discusses NPT and outlines how to protect patients and users from the risk posed by these devices.
Devices must be designed and manufactured in such a way that they perform appropriately for their
intended purpose taking into account the skills of the intended user and the potential for variation in
the user's technique and environment. The information and instructions for use (IFU) provided by
the manufacturer must be easy for the intended user to understand and apply in order to correctly
interpret the result provided by the device. Information regarding the level of training and
qualifications required by the user should also be provided in the IFU. Furthermore where feasible,
manufacturers must specify how the intended user can verify the device is performing as intended
by the manufacturer and provide information regarding detection of device failure. Any information
supplied must be provided in the language of the user. Finally a device must clearly state that the
device is for near patient testing and instructions for use must be supplied in paper format and not
only electronically.
6.4 Clinical data supporting safety and performance of IVDs
The IVDR sets high standards of quality and safety for IVDs by ensuring, among other things, that
data generated in performance studies is reliable and robust and that the safety of subjects
participating in performance studies is protected. The manufacturer must specify and justify the
level of clinical evidence necessary to demonstrate compliance with the relevant safety and
performance requirements which will be appropriate to the characteristics of the device, the
classification and its intended purpose. The manufacturers will then plan, conduct and document a
performance evaluation in accordance with Article 56 and with Part A of Annex XIII. The
performance evaluation is a continuous process and will need to assess and analyse three types of
clinical evidence; scientific validity, analytical performance and clinical performance.
6.5 HPRA safety notices, HPRA information notices and manufacturer field safety notices
The HPRA periodically issues safety notices in connection with issues that arise with NPT devices.
Information notices and other communications may also be issued.

44
In addition, manufacturers of NPT devices regularly issue FSNs (field safety notices) and other
instructions or information notices.
A system to review and take action on safety notices and other communications issued by the HPRA
and FSNs issued by NPT IVD manufacturers must be in place.
This includes procedures for traceability and implementation of Field Safety Corrective Actions for
NPT equipment, consumables and reagents where necessary.
6.6 Adverse incident reporting
An adverse incident is an event that causes, or has the potential to cause, unexpected or unwanted
effects. In the NPT environment this may involve the health and safety of patients, users or other
persons. For example, an incorrect result could lead to a delay in treatment, a life-threatening illness
or injury or a serious deterioration in the state of health, or even death.
All adverse incidents, in the first instance, should be made known as soon as possible to the NPT
operational team and to the designated NPT committee. The NPT IVD manufacturer will also be
informed where appropriate.
The manufacturer has a legal requirement in accordance with Article 11 of the IVD Directive
98/79/EC to report all adverse incidents that occur with IVDs on the Irish market to the HPRA. Any
adverse incident involving an IVD should also be reported by the organisation to the HPRA. Direct
reporting of adverse incidents by users to the HPRA is not mandatory but is strongly encouraged. It is
important that users are aware of the reporting requirements for adverse incidents under IVD
legislation and the key role they play to ensure that all incidents that occur on the Irish market are
reported to and investigated by the manufacturer.
With the introduction of the IVDR there will be a centralised electronic system called EUDAMED which
will allow manufacturers to report serious incidents and other reportable events. This will also allow
the public to be adequately informed about devices on the European market.
Recommendation 13. Report adverse incidents to the designated committee, the manufacturer
and the HPRA.
Further information including the HPRA form for reporting safety-related issues and adverse
incidents can be found on the HPRA website.
6.7 Unique Device Identification (UDI)
UDI is a system used to identify and facilitate traceability of IVDs within the healthcare supply chain.
Under the IVDR, manufacturers shall assign and maintain unique UDIs for their IVDs.

45
The UDI is a series of numeric or alphanumeric characters created through internationally accepted
device identification and coding standards and allows unambiguous identification of specific IVDs on
the market. Each IVD will have a UDI composed of two parts: a device identifier (UDI-DI) specific to
the model and packaging of the device, and a production identifier (UDI-PI) to identify the point of
manufacture.
The introduction of UDI under the IVDR should improve incident reporting, facilitate targeted field
safety corrective actions and lead to better monitoring by competent authorities.
It should also help to reduce medical errors and to fight against falsified IVDs. Use of the UDI system
should also improve purchasing and waste disposal policies and stock-management by health
institutions and other economic operators and, where possible, be compatible with other
authentication systems already in place in those settings.
Article 24 of the IVDR states in respect of UDIs:
 as part of the technical documentation referred to in Annex II, the manufacturer shall keep
up-to-date a list of all UDIs that it has assigned,
 economic operators shall store and keep, preferably by electronic means, the UDI of the
devices which they have supplied or with which they have been supplied,
 member states shall encourage, and may require, health institutions to store and keep,
preferably by electronic means, the UDI of the devices with which they have been supplied,
 member states shall encourage, and may require, healthcare professionals to store and
keep, preferably by electronic means, the UDI of the devices with which they have been
supplied with.
Although it has not yet been determined nationally what will be required of health institutions and
healthcare professionals in this regard, it is certainly preferable that local NPT managers would track
this information as good practice. In due course, the HPRA may issue further clarification on national
policy in this area. Further useful information is available at this link.
1. Unique Device Identification (UDI) System under the EU medical devices Regulations
2017/745 and 2017/746. European Commission website. Accessed 14/4/2021.

46
Chapter 7
ICT connectivity for NPT
Patient results must be recorded in the patient’s health record either manually or preferably
electronically.
Information and communication technologies (ICT) connectivity allows central recording of patient
results and quality parameters and should be resourced to a level which avails of the latest
technology including password-protection of equipment, operator identification, unique patient
identification, and integration of results with the patient’s electronic healthcare record. NPT IVDs
should be password-protected and only accessible by certified users.
Connectivity also facilitates remote monitoring of NPT equipment from a hub in the local laboratory
or manufacturer for quality assurance, governance, fault diagnosis, preventative maintenance, and
trouble-shooting in the event of problems.
7.1 Connectivity and the national medical laboratory information system (MedLIS)
Recommendation 14. Include all NPT results in the patient’s health record, ideally by
implementing ICT connectivity.
Connectivity between disparate computer systems and NPT analysers is an essential component for
provision of an effective NPT service within an organisation. In particular, it allows NPT IVDs to be
controlled and managed centrally and facilitates exchange of information from the remote NPT site
to the laboratory/hospital information system. Such connectivity is generally achieved through
deployment of a device management system, commonly referred to as “NPT middleware”. Key
connectivity goals are given in Table 7.1.
It is anticipated that the new national medical laboratory information system (MedLIS) will go-live in
2020. MedLIS aims to deliver a complete national pathology record for all patients in Ireland
including integration of NPT results. MedLIS will connect with NPT middleware systems and will not
interface directly to NPT IVD’s.
The national NPT consultative group recommends that a national NPT middleware system be
deployed such that all NPT results might be available in the national pathology record. Indeed,
without these results such a record would be incomplete. It is not financially viable, or technically
practical, for each organisation to procure, deploy and maintain its own NPT middleware.
Deployment of a national middleware solution would reduce duplication and mitigate redundancy in
connectivity systems. It would also enable integration of a patient’s NPT results from all settings so
as to be visible for clinicians in the patient’s pathology record.

47
Connectivity requirements for NPT were first identified as long ago as 2001 when a group of NPT
manufacturers known as the Connectivity Industry Consortium developed the POCT1-A standard
along with CLSI and other organisations. Though the groundwork for the original POCT1-A standard
was a USA initiative in 2000, a European initiative in 2001 led to internationalisation of the standard.
In 2006 the Clinical and Laboratory Standards Institute (CLSI) published an updated Point-of-Care
Connectivity Approved Standard POCT01-A2.
The objective of the standard is to allow seamless multi-vendor interoperability and communication
between NPT devices, data managers and clinical and/or laboratory information systems. The CLSI
asserts that this standard provides the framework for engineers to design devices, workstations, and
interfaces that allow multiple types and brands of NPT devices to communicate bi-directionally with
access points, data managers, and laboratory information systems from a variety of vendors.
Figure 5. ICT connectivity diagram for NPT
Also available from CLSI since 2008 is an implementation guideline on NPT connectivity for
healthcare providers (POCT02-A) which discusses the requirements of a connectivity-compliant
device, and it describes information that users should request from the supplier. These standards
remain relevant today and are a basis for multi-vendor interoperability and connectivity of NPT
devices if implemented by manufacturers.

48
TABLE 7.1
Key ICT connectivity goals
Positive identification of patient samples and patient demographics to the system.
Operator ID to allow traceability of results. Ideally the staff member’s bar-coded staff ID card,
registration number or similar device should be used.
Ideally identification of the UDI/equipment serial number should be captured.
Audit controls, logs, and accountability.
Password protected access to the system, login procedures and monitoring, and automatic logoff
settings.
Ability to clearly distinguish NPT results from other laboratory performed results on the
laboratory information system.
Integration of all results generated from NPT devices with the laboratory information system and
appropriate clinical information systems.
Appropriate data storage and backup.
Remote monitoring of NPT QC and IVD performance from the clinical laboratory.
Remote ability to temporarily block certified individuals who are not conforming to the stated IQC
protocol.
On-board decision support for order entry, and interpretation tailored to the analyser and
particular test.
Checking for data integrity.
Ability to perform patient audit and monitoring.
The extent to which this can be achieved depends on the particular NPT device, the number of
devices and the local healthcare IT services available. Use of laser technology to read bar-coded
patient identification on patient armbands, user identification badges and reagent/control
consumables has greatly reduced the risk of incorrect patient identification, uncertified user and
incorrect reagents/controls.
Incorrect transcribing of results or failure to record results is also being eliminated by the ability of
devices to transmit results to the laboratory information system/ electronic patient record.
7.2 Use of ICT for generating clinical alerts
Most NPT databases can be configured to generate user-friendly reports for clinicians, including daily
or periodic lists of abnormal glucometric or other NPT alerts1
to guide clinical teams.

49
1. Seheult JN, Pazderska A, Gaffney P, Fogarty J, Sherlock M, Gibney J, Boran G. Addressing
inpatient glycaemic control with an inpatient glucometry alert system. International Journal
of Endocrinology 2015, Article ID 807310. Accessed 14/4/2021.

50
Chapter 8
Implementing NPT services in primary care
and community settings
8.1 Clinical and managerial governance of NPT outside of hospital settings
It is important that primary and community care settings have a clearly defined and well-structured
approach to NPT to ensure that it is performed in a safe and effective manner and that the results
generated are accurate, reliable and recorded in the patient’s health record.
The best-practice goal for all NPT, regardless of where it is taking place, should be full accreditation
using the ISO 15189/22870 standards as implemented by INAB in Ireland.
This goal has been stated already in Chapter 1:
Services in Pharmacies from the Pharmaceutical Society of Ireland, and should be aiming
for ISO 15189/22870 accreditation as an ultimate goal.
It is acknowledged however that many NPT services (perhaps the majority) are not accredited today,
even in the hospital sector. Nevertheless, progress has been made in all sectors since the first edition
of this guideline in 2007 and all sectors have embarked on a journey where full accreditation is the
ultimate goal to optimise clinical outcomes and patient safety.

51
8.2 Recommendations for safe and effective NPT outside of hospital settings
The fourteen recommendations described in Chapter 1 (also shown here in Table 8.1) set out the
principles that also apply in the primary and community care sector and should be considered along
with the PSI guidance in the pharmacy sector.
Nevertheless, it is acknowledged that some modifications to the approach will be necessary to
reflect the different settings. For example, the NPT steering group will contain personnel relevant to
the sector though the presence of laboratory expertise and a laboratory consultant is strongly
recommended. Full details for each recommendation are given in the earlier chapters.
Prior to the implementation of a NPT service for a specific test, careful consideration should be given
to the ability of the local hospital laboratory to provide this service in a timely manner.
On consultation with the laboratory it may be agreed that the provision of a regular reliable courier
service and / or electronic ordering and result reporting can provide a turnaround time for patient
results by the laboratory which meets the requirements of the practice.
This in turn may negate the need for a near-patient test to be established in primary and community
care settings. National and international guidance should also be considered.
8.3 Self-audit checklist
It is advisable for NPT service providers to conduct a self-audit on a regular basis to ensure that the
NPT service being provided is accurate and reliable. The guidance for pharmacies issued by the PSI is
also useful in this regard and it also contains a self-assessment checklist.
Additionally, the checklist for the primary and community care sector included in Appendix 5 is a
useful guide to ensure the NPT service being provided is optimal.
8.4 Training and competency assessment
Training and competency assessment should be carried out as described in Recommendation 7. The
local laboratory can provide suitable documentation to record training, and an example of such a
document modified for the primary and community care sectors is shown in Appendix 6.
8.5 Premises
It is necessary to ensure that a designated area is available for the provision of a NPT service. This
should have suitable facilities for sample collection, NPT test execution, instrument storage, safe
disposal of sharps and clinical waste and storage of consumables under the appropriate conditions
as defined by the manufacturer. The area shall also ensure dignity and privacy for the patient. A
refrigerator may also be required for storage of certain NPT reagents which should include
temperature monitoring capability. In addition, consideration should be given to the environmental
conditions in which the NPT test and/or instrument is stored and operated, as incorrect temperature
and/or power supply conditions may impact the performance of the NPT test and hence the test
result.

52
TABLE 8.1
Governance
Commissioning
Implementation
Regulation
1. Establish an NPT Steering Group and organisation-wide NPT Policy
2. Consult with local laboratory
3. Document Case of Need involving all stakeholders
4. Establish an NPT operational team
5. Ensure all IVDs are CE marked, adequately validated and independently
verified
6. Develop standard operating procedures and protocols for all NPT
7. Ensure that anyone performing NPT is trained and demonstrated on-going
competence
8. Implement a quality assurance programme, including performance of
internal quality control and external quality assessment for all NPT
9. Ensure patient results are reviewed and interpreted by appropriately
qualified persons
10. Ensure full traceability of all IVDs used, including reagents and
consumables*
11. Ensure health and safety, and waste management training for staff*
12. Ensure all IVDs meet national and European IVD legislative requirements*
13. Report adverse incidents to the designated hospital committee, the
manufacturer and the HPRA
14. Include all NPT results in patient’s health record, ideally by implementing
ICT connectivity
* Recommendations 10, 11 and 12 are required for safe implementation of NPT, and are also regulatory requirements

53
8.6 Recent organisational developments in the primary care sector
Recent years have seen the introduction of new primary care centres around the country. These are
staffed by healthcare professionals including general practitioners, practice nurses, community
nurses, and other practice staff on a much larger scale compared with the previous model which had
higher volumes of small single-handed GP premises.
These new facilities offer opportunities to establish primary care diagnostic centres which could
provide safe and effective NPT provided there is a close link with the local hospital laboratory. This
link would be essential to secure INAB ISO 15189/22870 accreditation.
Community healthcare programmes, such as diabetes management or anticoagulant monitoring,
would benefit from the availability of key laboratory investigations at these centres and patients
would benefit from NPT.
There may also be potential in the largest of these facilities to provide satellite laboratory services
again linked to the local hospital.
8.7 Pharmacies
Testing services in pharmacies, including laboratory testing, has been addressed in the PSI Guidance
on Testing Services in Pharmacies.
NPT is being carried out in community pharmacies in a number of ways including:
1. Members of the public visit a pharmacy for screening tests such as for cardiovascular risk
(including lipid tests) or diabetes screening (including glucose and haemoglobin A1c tests).
2. Some pharmacists are performing NPT as part of a community anticoagulant monitoring
scheme under the auspices of the local anticoagulation service.
NPT services such as these should aim for full accreditation as the best-practice goal however as
a minimum a quality assurance programme should be implemented.
Where NPT testing is being used primarily for screening purposes as is usually the case in a
pharmacy setting, then a robust system of patient consent, follow-up and referral should be put
in place.
Appendix 5 provides a template for a patient evaluation form (including consent and relevant
medical and drug history), a template for a GP referral letter is given in Appendix 6, a checklist
for NPT implementation in primary/community care can be found in Appendix 7, and Appendix 8
contains a training record template.
1. Pharmaceutical Society of Ireland. Guidance on the provision of testing services in
pharmacies. Version 3, October 2019. PSI website. Accessed 14/4/2021

54
Concluding remarks
NPT has an important role to play in the delivery of an efficient healthcare service because of its
ability to provide a rapid test result in a timely manner in the immediate vicinity to the patient. This
may lead to increased clinical effectiveness and improved outcome for patients. However, this is
only true if the result delivered is accurate and reliable.
It is important that organisations have a clearly defined and well-structured approach to NPT to
ensure that it is performed in a safe and appropriate manner and conforms to acceptable analytical
and clinical standards.
Because there is a paucity of published literature regarding evidence-based support for NPT in
clinical management, it is incumbent on users to establish that their proposed NPT service will be
effective at a local level. There is a need for well-designed studies to evaluate clinical effectiveness of
NPT in relation to patient outcome.
It is recommended that these guidelines should be adopted by those responsible for NPT in Irish
healthcare organisations.
The implementation of these guidelines will facilitate a well-managed and appropriately governed
system for the provision of NPT services, which in turn will deliver considerable benefits to the Irish
health service and to patients.

55
Bibliography
1. In-Vitro Diagnostic Medical Device Regulation 2017/746/EU. HPRA website. Accessed 14/4/2021.
2. I.S. EN ISO 15189:2016 (Medical Laboratories - Requirements for quality and competence). NSAI
website (purchase required). Accessed 14/4/2021.
3. I.S. EN ISO 22870:2016. Point-of-care testing (POCT) - Requirements for quality and competence.
NSAI website (purchase required). Accessed 14/4/2021.
4. European Tissues & Cell Directive 2004/23/EU. Accessed 14/4/2021.
5. Regulation (EC) No 765/2008. EUR-Lex (Access to European law). Accessed 14/4/2021.
6. Guidance on the Provision of Testing Services in Pharmacies. Pharmaceutical Society of Ireland,
Version 3, October 2019. PSI website. Accessed 14/4/2021.
7. Definition, Diagnosis and Classification of Diabetes Mellitus and its Complications. Report of a
WHO Consultation. World Health Organisation, 1999. Accessed 14/4/2021.
management of diabetes mellitus. Diabetes Care 34(6): e61-99, 2011. Accessed 14/4/2021
9. General Data Protection Regulation: Information on EU data protection rules and GDPR
download (Irish version), European Commission. Accessed 14/4/2021.
10. HSE Password Standards Policy. HSE website. Accessed 14/4/2021.
11. Guidelines for Safe and Effective Management and Use of Near Patient Testing in Primary and
Community Care, 2008. HPRA website. Accessed 14/4/2021.
12. Guidelines for Safe and Effective Management and Use of Point of Care Testing. 2007. HPRA
website. Accessed 14/4/2021.
13. HSE standards for healthcare records management. Accessed 14/4/2021.
14. Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro
diagnostic medical devices. Accessed 14/4/2021
15. Minimum verification requirements for ISO 17025 & ISO 15189 testing laboratories (PS24). Irish
National Accreditation Board, PS24, Issue 1, 2016. Accessed 14/4/2021.
16. Guidance for the Assessment of Laboratories against EN ISO 15189 and EN ISO 22870 Point-of-
Care Testing (POCT). European Accreditation (EA) publication reference EA-4/20 G: 2014,
December 2014. Accessed 14/4/2021

56
17. Point-of-Care blood glucose testing in acute and chronic care facilities; Approved Guideline - 3rd
Edition (POCT12-A3). Clinical and Laboratory Standards Institute, 2013. ISBN 1562388673.
Accessed 14/4/2021.
18. Price CP, Hicks JM. Point-of-Care Testing: making innovation work for patient-centered care.
AACC Press, Washington DC, 2012. ISBN 9781594251436
19. Price CP, et al. Point-of-Care Testing: Needs, Opportunity, and Innovation. 3rd Edition, AACC
Press, Washington DC, 2010. ISBN 9871594251030
20. Point-of-care testing: principles and clinical applications. Luppa PB, Junker R (eds). Springer,
Berlin, 2018. ISBN 978-3-662-54496-9
21. Point-of-Care Connectivity; Approved Standard - Second Edition. CLSI document POCT01-A2.
Wayne PA: Clinical and Laboratory Standards institute; 2006. Sample only. Accessed 14/4/2021
22. Implementation Guide of POCT01 for Healthcare Providers; Approved Standard. CLSI document
POCT02-A. Wayne PA: Clinical and Laboratory Standards institute; 2008. Sample only. Accessed
14/4/2021
23. O’Kelly RA, Byrne E, Mulligan C, Mulready KJ, O’Gorman P, O’Shea P, Boran G. Is point of care
testing in Irish hospitals ready for the laboratory modernisation process? An audit against the
current national Irish guidelines. Ir J Med Sci (2013) 182:663-668. Accessed 14/4/2021
24. O'Kelly RA, Brady JJ, Byrne E, Hooley K, Mulligan C, Mulready K, O'Gorman P, O'Shea P, Boran G.
A survey of point of care testing in Irish hospitals: room for improvement. Ir J Med Sci. 2011
Mar;180(1):237-40. Epub 2010 Jul 27. PubMed PMID: 20661779. Accessed 14/4/2021
25. Seheult JN, Pazderska A, Gaffney P, Fogarty J, Sherlock M, Gibney J, Boran G. Addressing
Inpatient Glycaemic Control with an Inpatient Glucometry Alert System. Int J Endocrinol. 2015;
2015:807310. doi: 10.1155/2015/807310. Epub 2015 Jul 28. PubMed PMID: 26290664; PubMed
Central PMCID: PMC4531187. Accessed 14/4/2021
26. Cheng MP, et al. Diagnostic testing for severe acute respiratory syndrome-related coronavirus-2:
a narrative review. Ann Intern Med, April 13, 2020. DOI: 10.7326/M20-1301 (online). Accessed
14/4/2021

57
Appendices
Appendix 1. NPT steering group template
1. Terms of reference
1.1 The steering group will advise the management team on all aspects of NPT.
1.2 The steering group will provide clinical governance for the NPT service by ensuring that the
organisation’s systems and processes for monitoring and improving the quality of NPT services are in
accordance with best practice.
1.3 The steering group will develop and recommend policies and procedures for the proper conduct
of NPT, will be responsible for the review and commissioning of NPT services and may recommend
or commission focused research or development on aspects of NPT.
1.4 The existing range of NPT services will fall within the remit of the steering group, including [list of
analyses: e.g. blood gas analysis, blood glucose monitoring, pregnancy testing, and other analyses
requiring instrumentation]. A survey will determine the extent and risk category (low/medium/high)
of existing NPT including manual tests/dipsticks.
1.5 To review existing NPT services and receive proposals for new NPT services; and to assess the
case of need and clinical effectiveness for patients compared with other options for service delivery;
and to make recommendations as to their appropriateness, taking account of:
indications, contraindications and workload implications for NPT,
suitability, accuracy, limitations and scope of testing for clinical needs,
risk management and risk stratification of the various devices,
financial implications,
health and safety implications,
ability to audit quality and clinical effectiveness,
ability to trace and recall all IVDs, regents and consumables if required.
1.6 To implement a quality assurance programme for NPT including systems for internal and blind-
sample external quality assessment and adverse incident reporting, and taking into account:
operator training,
machine calibration and maintenance,
correct interpretation of results,
correct recording of results, including integration with IT systems,
health and safety requirements.
1.7 To implement an education programme for clinical users of NPT and to keep a list of trained
operators.
2. Membership
2.1 The minimum membership shall be [number locally defined], (quorum [number locally defined])
and shall serve for [duration defined locally] years.

58
The minimum steering group membership should consist of:
• A laboratory consultant from participating pathology/laboratory medicine disciplines,
• A senior management representative,
• A senior scientist from participating pathology/laboratory medicine disciplines,
• The manager of each or all NPT operational teams,
• Clinical risk manager,
• Senior medical representatives from participating services,
• Senior nursing representatives from participating services,
• ICT representative.
2.2 Other members may be co-opted as necessary.
2.3 In the event of an appointed member being unable to attend, a deputy may attend in his or her
place.
2.4 Dr [name of nominee], [job title], is nominated as the chairperson for a defined period.
3. Meetings
3.1 The steering group shall meet on a quarterly basis.
3.2 Additional meetings may be convened at the discretion of the chairperson to deal with urgent or
specific matters.
4. Operational teams
4.1 The steering group may appoint operational (working) teams to deal with specific issues and with
defined terms of reference. These groups will meet on an ad hoc basis according to the needs of the
specific project.
5. Reporting and review
5.1 The steering group will report to the executive management team.
5.2 This document and the terms of reference will be reviewed every 2 years to gauge effectiveness.

59
Appendix 2. User application form for a new NPT service
Proposals for new NPT require detailed consultation with the local laboratory service including a
laboratory medicine consultant from the appropriate pathology discipline.
The form is intended for initial completion by the end-user proposing the service, with assistance as
required from the NPT Team for detailed technical aspects. Input may also be required from other
services, including ICT and finance.
Please ensure the following form is completed prior to submission.
Checklist
(Applications cannot be considered without submission of all data specified)
Tick
1 Section 1, 2 and 3 fully completed and signed off by all parties. 
2 Supporting clinical documentation/validation data attached. 
3 Analyser verification data attached (if applicable). 
4 Completed ICT project mandate attached (if applicable). 
5 Approved business plan (to include all associated costs) attached. 
Section 1 – General information
 What test/test profile do you wish to perform as NPT? Please also specify sample type
requirements (i.e. whole blood, urine etc.).
Click or tap here to enter text.
 What department/area is requesting the service and who is the clinical director?
 Is testing currently performed in your local laboratory? Please state the clinical need for a
NPT service rather than a conventional laboratory service. Please attach any published
data/ validation in support of your claim (see checklist item 2).
 Name the laboratory medicine consultant with whom you have discussed your proposal
and attach their written opinion as part of the evidence submitted (see checklist item 2)
 Is testing currently performed in laboratory? Please state the clinical need for a NPT service
rather than a conventional laboratory service. Please attach any published data/ validation
in support of your claim (see checklist).
 What workload is envisaged in terms of specimen numbers per year?

60
 Specify who will hold clinical governance over the NPT results?
 Who will perform the testing?
 Will testing be performed out of hours (outside 09.00-17.00, Monday-Friday)?
 Where exactly will this new NPT service be performed and where will the NPT equipment
be located? (specify room number, ward etc.)
 Will NPT staff and equipment service engineers have easy access to the device(s)?
 Please identify a liaison person(s) in the area who will assist the NPT department in
delivering the service.
 Is testing currently performed in laboratory? Please state the clinical need for a NPT service
rather than a conventional laboratory service. Please attach any published data/ validation
in support of your claim (see checklist).
 What benefit will accrue to staff or patients through implementation of this NPT service?
 Identify any infection control issues. Ensure hospital policy is adhered to.
 Identify any health & safety issues. A risk assessment will be required prior to introduction
of service.
Section 2 – Equipment and IT
 Has a suitable device/instrument been identified? If ‘yes’, please supply details.
If ‘no’ then skip to section 3.
 Is the device currently in use? If ‘yes’ please attach method verification data. Also attach
correlation data with laboratory method, if applicable. Note: only electronic verification
and correlation data will be accepted as several statistical calculations are required as
mandated by ISO 22870 and ISO 15189.
 Is it possible to restrict equipment access to trained operators only? Is the instrument
password protected?

61
 Can the device be monitored remotely by the NPT department through the middleware
currently in use in NPT or with new middleware software?
 Can patient results be stored/ backed-up? If ‘yes’ how is this done and in what format is it
stored?
 Can the device be interfaced with the LIS (both existing and MedLIS)/HIS? Note: laboratory
policy requires interfacing of NPT equipment (where possible) to ensure complete
electronic patient record. ICT interfacing requires an ICT mandate form to be submitted to
ICT. Include ICT contact details if they have been consulted prior to submission of this
document (see checklist).
 Does the device require network points/Wi-Fi & power sockets? Please detail
requirements for the device and are they currently available in the desired location?
Section 3 – Finance
 Attach the business plan and has it been approved by your finance officer to cover all
associated costs of introducing this service? This must include the following:
a. What staff costs are involved (additional or existing, laboratory and/or clinical staff)?
b. What is the capital cost of the device/system including VAT?
c. If interface capability, include the cost associated with interfacing?
d. Include the cost of any ancillary hardware (e.g. printer, barcode reader, etc.) and
software (updates).
e. Include the cost of annual maintenance and servicing costs.
 Include details and costs of the external quality assessment scheme.
 Based on the projected test numbers and IQC requirements, what are the annual costs for
consumables and reagents?
 Any additional costs that may be associated with the device.

62
Signatures:
Date of application
Signature of applicant
Title of applicant
Contact details
Clinical consultant (if not the applicant)
Laboratory consultant
Laboratory chief medical scientist
For NPT team use only
1. Would other departments within the hospital have similar requirements for this service?
Click here to enter text.
2. Is the device CE marked?
3. Is there sufficient storage space for the device(s), consumables and reagents in the location
suggested?
4. Will the device have an uninterrupted power supply (UPS) unit?
5. If equipment is already in place, has a maintenance contract been agreed with the supplier/
manufacturer?
6. What response time is guaranteed with the supplier regarding repairs/ replacement and is
this a 24hour/ seven days a week agreement?
7. Who will provide operator training and competency assessment?

63
Appendix 3. NPT cost benefit analysis form

65
Appendix 4. Implementation checklist for an approved NPT Service
This form may be used as a checklist for the NPT Operational Team to assist with implementation of
a new approved NPT service. It is not intended for completion by the end-user.
1. Name and Description of NPT service to be provided
2. Is the test available in the laboratory for confirmatory purposes?
Yes No
3. State the clinical need for NPT rather than being supplied by the central laboratory.
4. Why is the laboratory unable to meet the requirements?
5. What measurable benefits of the NPT service can be monitored?
6. What workload is envisaged in terms of specimen numbers/month?

66
Space
7. Where do you want to locate the NPT; is it a safe working environment?
8. What size area is available for NPT?
9. What is the distance to the nearest sink?
10. What space is available for storage of stock items?
11. Is the room air-conditioned?
Yes No
12. Can an engineer have easy access to instruments?
Yes No
Equipment
13. Details of IVD
14. Has the discipline/laboratory confirmed the choice?
Yes No
15. What is the life expectancy of the device?

67
16. Is there data comparing the proposed NPT with the laboratory method?
Yes No
17. Has a risk assessment been completed? If so please attach.
Yes No
Costs/risks associated with device/equipment
18. What is the capital cost of the instrument including VAT?
19. What is the annual consumable cost?
20. What is the maintenance/servicing cost after guarantee?
21. Is the cost of interfacing the device to the laboratory computer included in the cost?
Yes
No If no, what is the cost to interface?
22. Is the cost of software and hardware to monitor and control the device from the central
laboratory included?
Yes No
23. Have you funds sanctioned to cover these costs?
Yes No
24. Does it have to go to EU tender?
Yes No

68
25. Is it CE marked?
Yes No
26. Can the device be decontaminated?
Yes No
27. What are the infection control issues?
28. What are the health and safety and occupational health issues?
Maintenance of the device
29. What response time is guaranteed in the maintenance contract?
30. Is this a 7 day week, 24 hour response?
Yes No
31. What are the implications for other support departments (e.g. laboratory disciplines
providing support, pharmacy, bio-engineering, etc.)?

69
32. Has out of hours support been agreed with the named support departments?
Yes No
33. Is the proposed equipment compatible with similar results produced elsewhere in the
hospital?
Yes No
34. Does the device have a UPS (uninterrupted power supply unit)?
Yes No
Responsible personnel
35. Who will be the designated person in charge of the device day to day?
36. Who will perform the test(s)?
37. Will you have designated staff to cover absences of the designated person responsible for
the device and for performing the test(s)?
Yes No
38. Is the instrument password-protected?
Yes No
39. Who takes responsibility for issuing and maintaining passwords?
40. Who takes responsibility for internal quality control programme of users?
41. Who takes responsibility for external quality assessment?

70
42. Who takes responsibility for clinical action based on the NPT result?
Interfacing and patient record
43. Can the instrument be monitored through designated software in the central laboratory?
Yes No
44. Can the device be interfaced with the laboratory computer?
Yes No
45. How will the patient record be stored?
46. Do you need ICT connectivity and support?
Yes No
47. Has the ICT department agreed to your requirements?
Yes No
Clinical governance
48. Are you compliant with the hospital NPT policies for governance?
Yes No
Traceability and Field Safety Corrective Actions
49. Describe the system for traceability of the IVD and/or associated reagents and consumables
that will apply for this NPT. Attach the inventory.

71
50. Describe how the IVD and/or associated reagents and consumables will be identified and
quarantined in the event of a patient safety-related incident.
Signatures
--------------------------------------------- ------------------
NPT Manager Date
--------------------------------------------- ------------------
Clinical Director or Division Head Date
--------------------------------------------- ------------------
Laboratory Consultant Date

72
Appendix 5. Patient evaluation form template (for non-GP based NPT settings)
Title:
First name:
Surname:
Date of birth:
Address:
GP name and address:
Date of assessment:
Are you aware of the significance of the test being performed and the consequences of an abnormal result?
Is there any relevant medical history you would like to disclose?
Is there any relevant medication history you would like to disclose?
Test
performed
Result Units Within acceptable limits
(Yes/No/N/A)
Additional information
(Test batch number / N/A
etc.)
Referral to be made (Yes/No).
If yes include reason for referral
NPT service provider (print sign & date):
NPT service provider position:
Do you consent to a referral?
Patient (print, sign & date):

73
Appendix 6. GP Referral letter template (for non-GP based NPT settings)
Dear Dr
Please be advised that (patient’s name) presented at (NPT location) on (date) and received the
following test (test name).
The result of this test was as follows: XXXXX. The test was performed on xxxx manufactured by xxxx.
The following information was also provided by the patient: XXXXX.
Other comments: XXXXX
The patient was informed that this referral letter would be written and was advised to contact their
own GP for follow-up.
Referee: Signed:
Referee position: Date:

74
Appendix 7. NPT primary/community care checklist
The following is a useful checklist for NPT providers and SOP authors.
Points to Consider Yes No N/A
1 Is the premises appropriate for the test being
performed? 


2 Is the test carried out in a private dedicated area
suitable for patient counselling? 


3 Is a shredder provided for disposal of waste paper
containing confidential patient information? 


4 Is access to patient records and confidential
information controlled? 


5 Are information leaflets available to patients?



6 Is the necessary testing equipment available and of
appropriate quality? 


7 Is the equipment maintained regularly to ensure it is
operating correctly? 


8 Is there suitable storage space for consumables and
reagent components requiring specialised storage, e.g.
quality control samples?



9 Are all materials stored in a manner which minimises
risk and is legislatively compliant? 


10 Are the relevant safety data sheets available (if
required)? 


11 Are suitable bins provided and is the disposal
mechanism for NPT waste in compliance with
environmental provisions?



12 Is a sharps container available?




75
13 Is a written procedure available and are staff trained in
the management of possible contaminated spillages? 


14 Are suitable procedures in place for transportation of
patient samples if required? 


15 Is there a structured quality assurance programme in
place and is it reviewed regularly? 


16 Is a self-audit regularly carried out by the manager to
review all aspects of the NPT service? 


17 Is personal protective equipment available (e.g.
gloves)? 


18 Are all products checked on receipt for quality,
quantity and expiry date? 


19 Are all IVDs CE marked and in compliance with the
relevant legislation? 


20 Are the devices maintained, calibrated and within
expiry? 


21 Is the NPT service provider trained and adequately
competent to perform all aspects of the test? 


22 Are patients advised of the requirements in advance of
a test? 


23 Has the patient completed an evaluation form?



24 Is the significance of the test result explained in a clear
and understandable manner? 


25 Are written procedures (SOPs) in place for the
execution of each test? 


26 Is the current version of the manufacturer’s
instructions for use (IFU) available? 


27 Is the test procedure quality assured?



28 Are instructions available for performing calibration
and quality control, including details of the material to
be used and the defined acceptable limits?




76
29 Are guidelines available on interpretation of
instrument error codes? 


30 Are guidelines available for interpretation of test
results? 


31 Is there a process for documenting adverse incidents
and reporting of adverse incidents to the HPRA and/or
other appropriate regulatory body?



32 Are results provided to the patient in a documented
format? 


33 Is there a procedure in place to inform staff of the
requirements in respect of patient referral? 


34 Are appropriate patient result records maintained?



35 Is there a process for co-operation with Field Safety
Corrective Actions such as product recalls? 


36 Is a documented staff training record maintained?



37 Is an on-going training programme provided for all
staff? 


38 Does on-going evaluation and monitoring of NPT
service provider performance occur? 


39 Does the training assess current and future
requirements and developments in the area? 


40 Do newly appointed staff members receive adequate
training? 


41 Are all staff aware of their professional role, the
associated boundaries and accountabilities? 



77
Appendix 8. Training record templates
A8.1 Training Record Template- Blood Gas Analysis (Analyser; Cartridge)
Title of Training Competent
(Initials)
Name of Device:
Model:
Trainer – Name:
NPT Team / Vendor:
Procedure (SOP)
Edition / Revision number
Training Date(s)
Training Duration (hrs/mins)
Training Method
Instructor led / E – Learning /Self train
Has the Trainee reviewed the relevant manufacturer’s instructions for use, SOP,
video training, working instructions, daily maintenance logs, and documentation
required?
Equipment
Can the Trainee identify all elements of the general operation of the equipment:
Equipment overview, screens, scanners
Calibration intervals ( automatic)
IQC intervals – automatic / scheduled manual requirements
Parameters measured on the equipment, parameter failure indicators
Basic principles of analysis

78
Stored results and review
IT Connectivity to other systems e.g. PAS, LIS, EPR, ISIP
Reagent Storage
Is the Trainee aware of the storage requirements for all reagents, IQC, reagent
cartridges etc.
IQC Performance
Is the Trainee aware of IQC performance requirements and intervals
Is the Trainee adequately competent to perform manual IQC if required and can
identify and action failures?
Is the Trainee aware of the requirement to document manual IQC performance
Contraindications and Interferences
Is the Trainee aware of pre- analytical interferences:
Infusion in situ and the effect of sample dilution
Unsuitability of any parameter in certain clinical scenarios (e.g. effect of
haemolyis, lipaemia)
Is the Trainee aware of the unsuitability of the equipment for certain sample
types ( e.g. Bone Marrow stab, urines, other)
Test interferences ( e.g. Ethylene Glycol)
Has the trainee read the manufacturer’s guidance on interferences?
Operator and Patient ID
Is the Trainee aware of the importance of Operator ID use and protection?
Is the Trainee aware of the importance of correct patient demographic entry as
per hospital / local guidance?
Specimen Collection
Is the Trainee aware of correct specimen collection techniques and specimen
requirements:
Syringes in use for Blood Gas analysis from all patient sites

79
Sample Collection processes from all sites e.g. Arterial, Arterial lines, CVP lines
Order of draw
Sample volume required for analysis
Sample preparation following draw including mixing and removal of all air
bubbles
Time to analysis and sample unsuitability
Transport requirements
Performing the Analysis
Has the trainee been observed performing the test?
Is the Trainee sufficiently competent to execute the test unsupervised?
Is the Trainee aware of their responsibilities in performing the test correctly and
observing best practice guidance?
Results/ Out of Range Results/Troubleshooting
Is the Trainee aware of result recording, interpretation, and result storage as per
hospital/ local policy and the need to re - check out of range and clinically
unexpected/ discrepant results with a Laboratory measurement?
Contact Details of the NPT Team
Is the Trainee aware of contact details of the NPT team for general advice,
equipment failures, unusual / spurious results; adverse incident reporting
Safety and Cleaning
Adheres to infection control guidelines and correct PPE
Disposal of samples and equipment as per hospital/ local guidelines

80
Knows the correct cleaning procedure for the equipment
Signatures
Is the Trainee aware of ongoing competency assessments and retraining?
Is the Trainee aware of National Policy Guidance for NPT Testing?
Is the Trainee aware of ISO 22870 Standard for NPT Testing?
Trainee’s name (Print)
Trainee’s Signature / Date
Instructor’s Name (Print)
Instructor’s Signature / Date
Refresher Training Due Date

81
A8.2 Training Record Template- Meter using Strips or Cassettes (e.g. Glucose, Urinalysis, Pregnancy
Testing, INR)
Title of Training Competent
(Initials)
Name of Device:
Model:
Trainer – Name:
NPT Team / Vendor:
Procedure (SOP)
Edition / Revision number
Training Date(s)
Training Duration (hrs/mins)
Training Method
Instructor led / E – Learning /Self train
Has the Trainee reviewed the relevant manufacturer’s instructions for use, SOP,
video training, working instructions, daily maintenance logs, and documentation
required?
The Meter
Can the Trainee identify all elements of the general operation of the equipment:
Equipment overview, screens, scanners
Calibration intervals (automatic)
IQC intervals – automatic / scheduled manual requirements
Parameters measured on the equipment, parameter failure indicators
Basic principles of analysis

82
Stored results and review
IT Connectivity to other systems e.g. PAS, LIS, EPR, ISIP
Reagent Storage
Is the Trainee aware of the storage requirements for all reagents, IQC, reagent
cartridges etc.
IQC Performance
Is the Trainee aware of IQC performance requirements and intervals
Is the Trainee adequately competent to perform manual IQC if required and can
identify and action failures?
Is the Trainee aware of the requirement to document manual IQC performance
Contraindications and Interferences
Is the Trainee aware of pre-analytical interferences:
Infusion in situ and the effect of sample dilution
Unsuitability of any parameter in certain clinical scenarios (e.g. effect of
haemolysis, peripheral infusion, limitations of urine hCG testing, hCG fragments
in molar pregnancy, antiphospholipid antibodies in INR)
Has the trainee read the manufacturer’s guidance on interferences?
Operator and Patient ID
Is the Trainee aware of the importance of Operator ID use and protection?
Is the Trainee aware of the importance of correct patient demographic entry as
per hospital / local guidance?
Specimen Collection and Performing a Blood Test
Is the Trainee aware of correct specimen collection techniques and specimen
requirements:
Sample volume required
Can insert strip/cassette correctly
Knows the recommended sampling times and rationale

83
Explains the procedure to patient as appropriate
Demonstrates the ability to use lancet correctly
Test interferences (e.g. use of alcohol swabs; manipulation of the test area –
squeezing the finger/site)
Performing the Analysis
Has the trainee been observed performing the test?
Is the Trainee sufficiently competent to execute the test unsupervised?
Is the Trainee aware of their responsibilities in performing the test correctly and
observing best practice guidance?
Results/ Out of Range Results/Troubleshooting
Is the Trainee aware of result recording, interpretation, and result storage as per
hospital/ local policy and the need to re - check out of range and clinically
unexpected/ discrepant results with a Laboratory measurement?
Contact Details of the NPT Team
Is the Trainee aware of contact details of the NPT team for general advice,
equipment failures, unusual / spurious results; adverse incident reporting
Safety and Cleaning
Adheres to infection control guidelines and correct PPE
Disposal of samples and equipment as per hospital/ local guidelines
Knows the correct cleaning procedure for the equipment

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Signatures
Is the Trainee aware of ongoing competency assessments and retraining
Is the Trainee aware of National Policy Guidance for NPT Testing?
Is the Trainee aware of ISO 22870 Standard for NPT Testing?
Trainee’s name (Print)
Trainee’s Signature / Date
Instructor’s Name (Print)
Instructor’s Signature / Date
Refresher Training Due Date
R31 G153 B51

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