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LIMS 
Ammara Ahmed 
Roll no. 1010 
BS (Hons.) Botany(M) 3rd Semester 
University of Education Okara.
Table of Contents 
• References 
• LIMS 
• Information Technology 
• General Consideration 
• Types of Labs (Research Labs) 
• Testing & Manufacturing Labs 
• LIMS Aquisitions
Laboratory Information 
Management Systems (LIMS) 
Lindy A. Brigham 
Div of Plant Pathology and Microbiology 
Department of Plant Sciences 
PLS 595D Regulatory Issues in Laboratory 
Management 
February 2, 2006
LIMS 
• Definition: 
– A method a laboratory uses to manage its 
data and disperse the results to designated 
areas
Information Technology 
• Why? 
– Management of the Information Explosion 
– Quality Assurance 
• GLP, GMP, EPA, etc. 
– Reduction of data entry errors 
– Need for faster sample/results turnaround 
time
General Considerations 
• Different labs have different requirements 
• Procedures and outcomes differ 
• But all can use the systems approach to 
identifying their needs and implementing 
solutions
Types of Laboratories 
• Research 
• Analytical Services 
• Manufacturing
Research Lab 
• Many non-routine tests 
• Low sample volume 
• Flexibility between data and analyses 
performed 
• Specification checking (FDA reqs) 
• Traceability (calibration, distribution, data) 
• Change control procedures (documentation 
of changes eg SOPs, QA compliance)
Testing Services Laboratory 
• Tests performed at customer’s request 
• High sample volume 
• Routine tests 
• Variable workload 
• Prioritized samples
Manufacturing Laboratory 
• Perform testing for various materials 
including: 
– Final product testing 
– Stability testing 
– Work-in-progress testing 
– Environmental testing 
– Raw materials acceptance testing 
• Many tests per sample 
• Dynamic environment
LIMS Acquisition 
• How do you determine what you need and 
how to get it? 
• Systems Approach to defining needs and 
specifications for a LIMS
Acquisition Decisions 
• Buy or Build? All or Pieces? 
• Options 
– Design and build system ‘from scratch’ 
– Piece together existing and off the shelf 
components 
– Buy whole system from vendor 
• How do you decide?
By doing an Analysis 
• The build or buy or buy what decision is 
made based on an analysis of the needs 
and practices of the lab 
• The analysis itself can be of benefit to any 
lab to: 
– Clarify existing practices 
– Help eliminate non-essential practices 
– Organize and streamline existing procedures
Systems Analysis and Design 
• Project Definition 
– What is to be achieved, by whom and why 
• Functional Requirements 
– all user entry requirements and system output requirements described 
in detail 
• Functional Design 
– detailed documentation to describe the system and detail how the 
functional requirements are to be achieved – independent of hardware 
and software requirements 
• Implementation Design 
– selection of hardware and software 
• System Integration 
– Gather all required components, interface components, install software, 
go live 
• System Evaluation 
– Final phase 
– Project definition and functional requirements are revisited and 
compared to the final installed system to determine how well the 
requirements were met
Workflow Overview – Research
Workflow Overview – Analytical
Information Management System 
• Consists of: 
– Computer(s) 
– People 
– Procedures/Processes
LIMS Resources 
• Stand alone software 
– All purpose 
• Word Processing 
• Spreadsheets 
• Databases 
– Inventory 
– Document Management (Wolk) 
– Statistical Packages 
• Total systems 
– Lablynx http://www.lablynx.com/ 
– Starlims http://www.starlims.com/
Regulatory Requirements 
• ISO 9000 
– Management must define, implement, communicate and 
maintain quality objectives and assign personnel at all levels of 
the organization to be responsible for verifying the company’s 
quality system 
– Primarily effect manufacturing laboratories 
• ISO 25 
– Establishes labs technical competence 
• GALP (Good Automated Laboratory Practices) 
– Union of federal regulations, policies, and guidance documents 
establishing a uniform set of procedures to ensure the reliability 
and credibility of laboratory data (EPA) 
• 21 CFR 11 (1997) 
– Electronic signatures, Electronic records

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LIMS

  • 1. LIMS Ammara Ahmed Roll no. 1010 BS (Hons.) Botany(M) 3rd Semester University of Education Okara.
  • 2. Table of Contents • References • LIMS • Information Technology • General Consideration • Types of Labs (Research Labs) • Testing & Manufacturing Labs • LIMS Aquisitions
  • 3. Laboratory Information Management Systems (LIMS) Lindy A. Brigham Div of Plant Pathology and Microbiology Department of Plant Sciences PLS 595D Regulatory Issues in Laboratory Management February 2, 2006
  • 4. LIMS • Definition: – A method a laboratory uses to manage its data and disperse the results to designated areas
  • 5. Information Technology • Why? – Management of the Information Explosion – Quality Assurance • GLP, GMP, EPA, etc. – Reduction of data entry errors – Need for faster sample/results turnaround time
  • 6. General Considerations • Different labs have different requirements • Procedures and outcomes differ • But all can use the systems approach to identifying their needs and implementing solutions
  • 7. Types of Laboratories • Research • Analytical Services • Manufacturing
  • 8. Research Lab • Many non-routine tests • Low sample volume • Flexibility between data and analyses performed • Specification checking (FDA reqs) • Traceability (calibration, distribution, data) • Change control procedures (documentation of changes eg SOPs, QA compliance)
  • 9. Testing Services Laboratory • Tests performed at customer’s request • High sample volume • Routine tests • Variable workload • Prioritized samples
  • 10. Manufacturing Laboratory • Perform testing for various materials including: – Final product testing – Stability testing – Work-in-progress testing – Environmental testing – Raw materials acceptance testing • Many tests per sample • Dynamic environment
  • 11. LIMS Acquisition • How do you determine what you need and how to get it? • Systems Approach to defining needs and specifications for a LIMS
  • 12. Acquisition Decisions • Buy or Build? All or Pieces? • Options – Design and build system ‘from scratch’ – Piece together existing and off the shelf components – Buy whole system from vendor • How do you decide?
  • 13. By doing an Analysis • The build or buy or buy what decision is made based on an analysis of the needs and practices of the lab • The analysis itself can be of benefit to any lab to: – Clarify existing practices – Help eliminate non-essential practices – Organize and streamline existing procedures
  • 14. Systems Analysis and Design • Project Definition – What is to be achieved, by whom and why • Functional Requirements – all user entry requirements and system output requirements described in detail • Functional Design – detailed documentation to describe the system and detail how the functional requirements are to be achieved – independent of hardware and software requirements • Implementation Design – selection of hardware and software • System Integration – Gather all required components, interface components, install software, go live • System Evaluation – Final phase – Project definition and functional requirements are revisited and compared to the final installed system to determine how well the requirements were met
  • 16. Workflow Overview – Analytical
  • 17. Information Management System • Consists of: – Computer(s) – People – Procedures/Processes
  • 18. LIMS Resources • Stand alone software – All purpose • Word Processing • Spreadsheets • Databases – Inventory – Document Management (Wolk) – Statistical Packages • Total systems – Lablynx http://www.lablynx.com/ – Starlims http://www.starlims.com/
  • 19. Regulatory Requirements • ISO 9000 – Management must define, implement, communicate and maintain quality objectives and assign personnel at all levels of the organization to be responsible for verifying the company’s quality system – Primarily effect manufacturing laboratories • ISO 25 – Establishes labs technical competence • GALP (Good Automated Laboratory Practices) – Union of federal regulations, policies, and guidance documents establishing a uniform set of procedures to ensure the reliability and credibility of laboratory data (EPA) • 21 CFR 11 (1997) – Electronic signatures, Electronic records