Orlando Lopez

Pharmaceutical and Medical Devices Manufacturing Computer Systems Validation

• Broschiertes Buch

Produktbeschreibung

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. Compliance is a state of being in

---

Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.

Produktdetails

• Verlag: Taylor & Francis Ltd
• Seitenzahl: 344
• Erscheinungstermin: 30. Juni 2021
• Englisch
• Abmessung: 175mm x 254mm x 32mm
• Gewicht: 648g
• ISBN-13: 9781032094700
• ISBN-10: 1032094702
• Artikelnr.: 62153114

Autorenporträt

Orlando López E-records Integrity SME Durham North Carolina USA Orlando Lopez has significant understanding and experience with worldwide regulatory authorities regarding CSV, e-records integrity, and related requirements/guidelines related to Production Manufacturing Systems, IT Systems, Analytics, and Business Intelligence. He has knowledge and experience in the development of governance and SLC deliverables. Wrote and deployed CSV methodology to computer infrastructure J&J worldwide. Several times he had re-engineered the computer validation methodology to regulated companies. Orlando Lopez has experience with direct participation in FDA agency remedial action plans, regulatory inspections, response activities, and consent decree remediation related verifications. He is published in the Encyclopedia of Pharmaceutical Science and Technology, 4th Edition - Chapter 56 Computer Systems Validation (Taylor & Francis Group, LLC) and had written 25+ publications, including 9 computer compliance related books - amazon.com/author/orlandolopez/ Familiar with gap assessment, remediation planning and remediation execution activities.

Inhaltsangabe

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