Three-Day Training Course on Virtual Computer Systems (CSV) Validation: Principles, Methods and Best Practices

DUBLIN, December 6, 2021 / PRNewswire / – Last days to register for the “Computer system validation training (CSV)” training course has been added to offer. This course is designed to fully immerse you in the principles, methods and best practices of Computer System Validation (CSV).

You will learn about the regulations that impact your systems and practice writing validation documents. You’ll leave ready to lead efficient, effective, and inspection-ready validation projects, whether you choose to follow a traditional waterfall or agile methodology.

The training camp is difficult and stimulating. This is a comprehensive three-day immersion in the validation process, including industry best practices and the latest technological advancements. Participants will perform hands-on validation activities through instructions, exercises and case scenarios.

Learning objectives

  • Understanding of how to comply with key FDA and international CSV regulations and guidelines, such as 21 CFR Part 11 and Annex 11
  • The purpose of each validation deliverable and the practical practice of creating each deliverable, including the validation plan, specification of requirements, test plan, validation tests (IQ, OQ, PQ), trace, test summary and validation report
  • Understanding of risk-based validation techniques and how to take advantage of these techniques to create effective yet compliant validation approaches
  • Appropriate validation strategies for many types of applications including Cloud / SaaS, COTS, spreadsheets and custom developed systems
  • Knowledge of best practices and inspector expectations for computer systems validation and software quality assurance (SQA) programs

Main topics covered:

AGENDA – Day 1

  • Module 1: Computer System Validation Regulations (CSV) 12:30 p.m. EDT

    • FDA regulations and guidelines
    • Other regulations and directives (EMA, ICH, EU, MHRA, PIC / S)
    • Exercise: Explore the regulations using the website
  • Module 2: Method and models for validation of the computer system 1:30 p.m. EDT

    • Validation, verification and qualification
    • Common SDLC
    • Model GAMP 5 “V”
    • COTS, Cloud, SaaS, PaaS, IaaS
    • Validation of the worksheet

To break 2:45 p.m. EDT 15 minutes

  • Module 3: 21 CFR Part 11:00 a.m. – 3:00 p.m. EDT

    • 21 CFR Part 11 Guidelines
    • Requirements for electronic records / signatures
    • Exercise: FDA Guidelines for ER / ES
  • Data integrity and governance – 4:00 p.m. EDT

  • End of session time: 5:00 p.m. EDT

AGENDA – Day 2

  • Module 4: Planning for validation – 12:30 p.m. EDT

    • Validation Strategy Document
    • Components of the validation strategy
    • Justification of validation tests
    • Categorization of the GAMP 5 system
  • Module 5: Risk Based Validation – 2:15 p.m. EDT

    • Risk assessment
    • Risk mitigation
    • Exercise: Writing the validation plan

To break – 3:00 p.m. EDT

  • Module 6: Requirements – 3:15 p.m. EDT

    • Requirements development
    • User Requirements Specification (URS)
    • Functional Requirements Specification (FRS)
    • Exercise: URS / FRS requirements interviews and drafting
  • Module 7: System Design and Development – 3:40 p.m. EDT

    • System Design Configuration (SDS)
    • Configuration Management Specification (CMS)
  • Module 8: Protocols and execution IQ, OQ, PQ – 4:00 p.m. EDT

    • Validation test process
    • Objective and content of the IQ
    • Objective and content of the OQ
    • Purpose and content of the PQ
  • Module 9: Validation test plan

    • Principles of validation testing
    • Testing techniques
    • Objective and content of the test plan
    • Exercise: Writing a test plan
  • Module 10: IQ, OQ, PQ protocols

    • Structure and content of the protocol
    • Objective proof
    • Test good writing practices
    • Test the good practices of the structure
    • Exercise: writing IQ / OQ / PQ
  • Module 11: Running the Tests

    • Good test execution practices
    • Documentation of validation failure
    • Exercise: Running the validation test
  • End of session time: 5:00 p.m. EDT

AGENDA – Day 3

  • Module 12: Requirements Traceability Matrix (RTM) 12:30 p.m. EDT

    • Purpose and content of Trace Matrix
    • Exercise: writing the trace matrix
  • Module 13: Test and Validation Reports – 12:45 p.m. EDT

    • Objective and content of the test summary
    • Purpose and content of the validation report
    • Exercise: Writing the validation summary report
  • Module 14: Change management 1:00 p.m. EDT

Break at 2:30 p.m. EDT 15 minutes

  • Module 16: FDA warning letters 2:45 p.m. EDT

    • Current trends in compliance and enforcement
    • Case Study: FDA Law Enforcement
    • Exercise: Be the consultant
  • Module 17: Q / A session and CSV exam 4:00 p.m. EDT

    • Activity: Preparation for the exam
    • Final exam
    • Q&A session with the course instructor

End of session time: 5:00 p.m. EDT

For more information on this training, visit

Media contact:
Research and markets
Laura Wood, senior
[email protected]

For EST office hours, call + 1-917-300-0470
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Fax (outside the United States): + 353-1-481-1716

SOURCE Research and Markets

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