Description

Book Synopsis

Validation of computer systems is the process that assures the formal assessment and report of quality and performance measures for all the life-cycle stages of software and system development, its implementation, qualification and acceptance, operation, modification, requalification, maintenance and retirement (PICS CSV PI 011-3). It is a process that demonstrates the compliance of computer systems functional and non-functional requirements, data integrity, regulated company procedures and safety requirements, industry standards, and applicable regulatory authority's requirements. Compliance is a state of being in adherence to application-related standards or conventions or regulations in laws and similar prescriptions.





This book, which is relevant to the pharmaceutical and medical devices regulated operations, provides practical information to assist in the computer validation to production systems, while highlighting and efficiently integrating wo

Table of Contents

Preface

1. Introduction

2. What Is a Computer Systems Validation (CSV)?

3. CGMP Regulatory Requirements for Production Computer Systems

4. Maxims in CSV

5. General CSV Principles

6. System Life Cycle

7. SLC Documentation

8. Management of the Computer System Requirements

9. Risk Based Validation

10. CSV Plans and Schedules

11. Project Management, SLC, Production CSV, ITIL

12. Computer Systems Operational Life

13. Suppliers and Service Providers

14. Trustworthy Computer Systems

15. Control of Data and Records

16. Technologies Supporting Integrity of E-Records

17. Infrastructure Qualification Overview

18. Remediation Projects

19. Production CSV Program Organization

20. Integration Between Computer System and E-Records Life Cycles

21. Digital Date and Time Stamps

22. New Technologies and Critical Processes

23. All Together

Appendix I: Glossary of Terms

Appendix II: Abbreviations and/or Acronyms

Appendix III: Regulatory Cross Match

Appendix IV: Additional Readings

Appendix V: References Papers—E-Records Integrity

Appendix VI: Case Study—Cloud-Based SCADA

Index

Pharmaceutical and Medical Devices Manufacturing

    Product form

    £31.34

    Includes FREE delivery

    RRP £32.99 – you save £1.65 (5%)

    Order before 4pm tomorrow for delivery by Sat 27 Jun 2026.

    A Paperback by Orlando Lopez

    15 in stock


      View other formats and editions of Pharmaceutical and Medical Devices Manufacturing by Orlando Lopez

      Publisher: Taylor & Francis Ltd
      Publication Date: 6/30/2021 12:00:00 AM
      ISBN13: 9781032094700, 978-1032094700
      ISBN10: 1032094702

      Description

      Book Synopsis

      Validation of computer systems is the process that assures the formal assessment and report of quality and performance measures for all the life-cycle stages of software and system development, its implementation, qualification and acceptance, operation, modification, requalification, maintenance and retirement (PICS CSV PI 011-3). It is a process that demonstrates the compliance of computer systems functional and non-functional requirements, data integrity, regulated company procedures and safety requirements, industry standards, and applicable regulatory authority's requirements. Compliance is a state of being in adherence to application-related standards or conventions or regulations in laws and similar prescriptions.





      This book, which is relevant to the pharmaceutical and medical devices regulated operations, provides practical information to assist in the computer validation to production systems, while highlighting and efficiently integrating wo

      Table of Contents

      Preface

      1. Introduction

      2. What Is a Computer Systems Validation (CSV)?

      3. CGMP Regulatory Requirements for Production Computer Systems

      4. Maxims in CSV

      5. General CSV Principles

      6. System Life Cycle

      7. SLC Documentation

      8. Management of the Computer System Requirements

      9. Risk Based Validation

      10. CSV Plans and Schedules

      11. Project Management, SLC, Production CSV, ITIL

      12. Computer Systems Operational Life

      13. Suppliers and Service Providers

      14. Trustworthy Computer Systems

      15. Control of Data and Records

      16. Technologies Supporting Integrity of E-Records

      17. Infrastructure Qualification Overview

      18. Remediation Projects

      19. Production CSV Program Organization

      20. Integration Between Computer System and E-Records Life Cycles

      21. Digital Date and Time Stamps

      22. New Technologies and Critical Processes

      23. All Together

      Appendix I: Glossary of Terms

      Appendix II: Abbreviations and/or Acronyms

      Appendix III: Regulatory Cross Match

      Appendix IV: Additional Readings

      Appendix V: References Papers—E-Records Integrity

      Appendix VI: Case Study—Cloud-Based SCADA

      Index

      Recently viewed products

      © 2026 Book Curl

        • American Express
        • Apple Pay
        • Diners Club
        • Discover
        • Google Pay
        • Maestro
        • Mastercard
        • PayPal
        • Shop Pay
        • Union Pay
        • Visa

        Login

        Forgot your password?

        Don't have an account yet?
        Create account