EU Variations & Renewals

REGULATORY AFFAIRS – EUROPE
EU: Variations to Marketing Authorisation
- By Mr. Sachin M. Chede
- Date : 18-12-2014

VARIATION
 What is a Variation….?
A variation to the terms of a marketing authorization is an amendment to the contents of
the documents of the approved dossier.
Variations in European Union (EU) are regulated by following regulations and Guidelines:
• Commission Regulation (EC) No. 712/2012 of 3 August 2012 amending Regulation (EC)
No. 1234/ 2008 concerning examination of variations to the terms of marketing authorisations
for medicinal products for human use and veterinary medicinal products.
Annex I – Extensions of marketing authorisations.
Annex II – Classification of variations.
Annex III – Cases for grouping variations.
Annex IV – Elements to be submitted.
Annex V – Variations concerning a change to or addition of therapeutic indication, addition of
non-food producing target species, replacement or addition of a stereotype, strain, antigen etc.
• Guidelines of 16.05.2013 on the details of the various categories of variations, on the
operation of the procedures laid down in Chapters II, IIa, III and IV of Commission Regulation
(EC) No 1234/2008 of 24 November 2008 concerning the examination of variations to the
terms of marketing authorisations for medicinal products for human use and veterinary
medicinal products and on the documentation to be submitted pursuant to those procedures.
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Variation classification guideline for European Union
3
http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/q_and_a/q_and_a_detail_000019.js
p&mid=WC0b01ac0580023b12

VARIATION
In general changes are categorized into three types:
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TYPES OF VARIATIONS
Variations are classified into following types -
5
Variations
Type IB
(Minor
variation)
Type II
(Major
variation)
Extension
(new
application)
Type IA
(Minor
variation)

TYPES OF VARIATIONS
 Variations are broadly classified in to two categories:
• Minor Variations: Type-1A & Type-1B variations
• Major Variations: Type-II variations
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Type IA variations
 Type lA variations: Type lA variations are the minor variations which have only a minimal impact or no
impact at all, on the quality, safety or efficacy of the medicinal product, and do not require prior approval
before implementation ("Do and Tell" procedure).
Such a minor variations are “classified” two subcategories, which impact on their submission:
• Type lA variations requiring immediate notification (‘IA IN‘)
• Type lA variations NOT requiring immediate notification (‘lA’) (Variations which do not require immediate
notification may be submitted by the marketing authorisation holder (MAH) within 12 months after
implementation).
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Type IA variations
 Why certain minor variations of Type IA require immediate notification ?
Certain minor variations of Type IA require immediate notification after implementation, in order to ensure
the continuous supervision of the medicinal product.
 When should I submit my Type IAINvariation?
This should be submitted immediately and generally within 2 weeks of implementation of the change.
 What is meant by 'implementation' for Type IA variations?
For quality changes, implementation is when the company makes the change in its own quality system.
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EXAMPLES OF TYPE IA VARIATIONS
Type IA Changes - Only a minimal impact or no impact at all, on the quality, safety or efficacy of the
medicinal product ("Do and Tell" procedure ):
 Examples of Type IAIN variation:
 Change in the name and/or address of the marketing authorisation holder
 Change in the name and/or address of a manufacturer/importer of the finished product (including batch
release or quality control testing sites)
 Changes in imprints, bossing or other markings
 Change in the shape or dimensions of the pharmaceutical form perticularly Immediate release tablets,
capsules, suppositories and pessaries.
 Examples of Type IAvariation:
 Addition of physico-chemical test in specification.
 Deletion of non-significant test (ex: Identification test in Stability study).
 Tightening of specification limits (ex: Tightening of test limit for water content, Residual solvents and Related
substances..etc.
 CEP updates/renewal.
 API and FP Batch size increase/decrease within 10 fold.
9

Type IB variations
• Commission Regulation (EC) No 1234/2008 ('the Variations Regulation') defines a minor variation or Type
1B as a variation which is neither a Type lA variation nor Type II variation nor an Extension.
• Such minor variations must be notified to the National Competent Authority/European Medicines Agency by
the Marketing Authorisation Holder (MAH) before implementation.
• However, the MAH must wait a period of 30 days to ensure that the notification is acceptable by the Agency
before implementing the change (Tell, Wait and Do procedure).
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EXAMPLES OF TYPE IB VARIATIONS
Type IB Changes - Min to moderate impact on product quality (Tell, Wait and Do procedure):
 Major change the approved Analytical method
 FP Mfg. site changes
 Shelf-life extension
 Change in storage condition
 Minor changes to approved manufacturing process
 Change in batch size beyond 10 fold category
 SmPC /PIL changes in-line with innovator product
11

Type II variations
• Commission Regulation (EC) No 1234/2008 ('the Variations Regulation') defines a major variation of Type II
as a variation which is not an extension and which may have a significant impact on the Quality, Safety or
Efficacy of a medicinal product.
EXAMPLES OF TYPE II VARIATIONS
Type II Changes (Significant impact on product quality, safety & efficacy):
 Addition of alternate/new API DMF supplier
 Relaxation of approved specification
 Major change in approved manufacturing process
 Major change in approved composition
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Extension Applications
• Definition for Extension of marketing authorisation:
Changes to a marketing authorisation listed in Annex I of Commission Regulation (EC) No 1234/2008
are regarded as "extensions" of the marketing authorisation.
Examples of extension changes:
1. Changes to the active substance(s)
- replacement of a chemical active substance by a different salt/ester complex/derivative. with the same
therapeutic moiety, where the efficacy/safety characteristics are not significantly different;
2. Change to strength, pharmaceutical form, route of administration
• Change of bioavailability;
• Change of pharmacokinetics e.g. change in rate of release;
• Change or addition of a new strength/ potency;
• Change or addition of a new pharmaceutical form;
• Change or addition of a new route of administration.
• Such applications will be evaluated in accordance with the same procedure as for the granting of the initial
marketing authorisation to which it relates.
• The extension can either be granted as a new marketing authorisation or will be included in the initial
marketing authorisation to which it relates.
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CHANGE/VARIATION IMPLEMNTATION CRITERIA
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Grouping of variations
• It is possible to group variations of different categories the same marketing authorisation (MA) and submit
them in one submission, under a single application form, to the same relevant authority. This is permissible
where variations are covered under the cases listed in Annex Ill to the variations regulation.
• Examples are any group of lA changes, a group comprising a Type IB or Type II change plus one or more of
the same or lower category which are consequential to the first, and a group of administrative changes to
labelling.
• If a projected group is not listed in Annex Ill, the regulation and supporting guidances permit the MAH to
request agreement of the relevant authority(ies) to grouping of related changes where a single data package
and evaluation are meaningful.
• 14 cases of Groupings listed in Annex Ill
• CMDh Guidance for Examples for Acceptable and Not-Acceptable Groupings for MRP/DCP Products
-Doc. Ref: CMDh/173/2010/Rev.10 July 2013
15

Documentation required for variation filling
 The following documents should be submitted for filing of Variations applications:
• Cover letter.
• The completed EU variation application form
• Reference of variation guidelines, indicating that all conditions and documentation requirements are met.
• Relevant documentation in support of the proposed variation including any documentation specified in the
Annex to these guidelines.
• In case that the variations affect the summary of product characteristics, labelling or package leaflet:
the revised product information presented in the appropriate format.
• Update or Addendum to the detailed critical summaries (quality, safety, efficacy as appropriate)
Examples of the variation applications:
Type IA
Type IB
Type II
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VARIATION APPROVAL TIMELINE
How shall my Type IA/ IAin notification be processed (timetable) by
Health Authority?
A ‘notification of receipt’ letter would be issued by the Agency within five days of receipt of a Type IA
application.
Within 30 days of receipt, the notification would be reviewed. The Health authority will check the correctness of
the application form, ensure the required documentation is present and compliance with the required
conditions.
The outcome of the process, an approval and/or refusal, would be communicated to the MAH via the post or
the portal.
There will be no interaction with the marketing authorisation holder (MAH) during the procedure, and no
request to provide missing information
Type IA notification is a ‘Do and tell’ procedure, therefore changes must be implemented prior to submission of
notification.
17

How shall my Type IB notification be processed (timetable) by Health
Authority?
For Type IB notifications, the target pre-assessment processing time is 14 days.
Substantive assessment is done within 30 days, and leads either to approval or a request for further
information (RFI) letter within that 30 days.
The company’s response to the RFI letter needs to be received within 30 days.
Assessment of that response is within a further 30 days.
18

How shall my Type II notification be processed (timetable) by Health
Authority?
Type II variations follow a 30-day, 60-day or 90-day procedure (Depending upon complexity of the variation
application)
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Important Links
MHRA FAQs for variations submitted after 1 January 2010:
http://www.mhra.gov.uk/Howweregulate/Medicines/Licensingofmedicines/Marketingauthorisations/Variationstoli
cences/FAQsforvariationssubmittedafter1January2010/Administrativechanges/
MHRA Variations to licences: Administrative FAQs:
cences/FAQsforvariationssubmittedafter1January2010/Administrative/index.htm
MHRA Variations to licences: Quality changes FAQs:
cences/FAQsforvariationssubmittedafter1January2010/Qualitychanges/index.htm
MHRA Variations to licences: MHRA experiences:
cences/Experiencetodate/index.htm
MHRA Variations to licences: Grouping & work-sharing:
cences/QualityAuditReportofNewTIANotifications/index.htm
CMDH Variation Procedure:
http://www.hma.eu/96.html
EMEA post authorisation Question & Answers:
http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/q_and_a/q_and_a_detail_000019.jsp&mid=W
C0b01ac0580023b12
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REGULATORY AFFAIRS – EUROPE
Marketing Authorisation Renewals in EU
Date:

EU: Renewals
Introduction
• A marketing authorisation is valid for five years, and is renewable upon application by the Marketing
Authorisation Holder.
• Once renewed the marketing authorisation will be valid for an unlimited period, unless the competent
authority decides, on justified grounds relating to pharmacovigilance.
• The authorisation may be renewed upon application by the marketing authorisation holder at least nine
months before its expiry.
• In the case a MAH does not submit the renewal application, the MA will expire by law
• Certain changes to the marketing authorisation particulars may be made at renewal, and these changes
shall not trigger a variation procedure.
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EU: Renewals
Renewal applications should be submitted in EU-CTD format and have to contain following modules:
 Module 1
 Module 2
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EU Variations & Renewals

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