Developing an ISO 13485-certified quality management system : an implementation guide for the medical-device industry /
This book details the lessons learned from a real-world project focusing on building an ISO 13485:2016 Quality Management System (QMS) from scratch and then having it officially certified. It is a practical guide to building or improving your existing QMS with tried and tested solutions. The book ta...
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| Format: | eBook |
| Language: | English |
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New York, NY :
Routledge, Taylor & Francis Group,
2022.
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| Online Access: | Connect to the full text of this electronic book |
Table of Contents:
- Chapter 1: About this bookChapter 2: IntroductionChapter 3: What to know before getting startedChapter 4: Getting startedChapter 5: Writing the quality manualChapter 6: Writing the Standard Operating ProceduresChapter 7: QMS documentation (SOP-1)Chapter 8: CAPA, monitoring & improvement (SOP-2)Chapter 9: Infrastructure (SOP-3)Chapter 10: Human resources (SOP-4)Chapter 11: Suppliers & distributors (SOP-5)Chapter 12: Auditing (SOP-6)Chapter 13: Communication, marketing & sales (SOP-7)Chapter 14: Risk management (SOP-8)Chapter 15: Clinical evidence (SOP-9)Chapter 16: Product realization (SOP-10)Chapter 17: Regulatory affairs (SOP-11)Chapter 18: Post-market surveillance (SOP-12)Chapter 19: Finalizing all the SOPsChapter 20: Writing templates, forms, records, and registriesChapter 21: Writing meeting agendas and minutesChapter 22: QMS software validationChapter 23: The launchChapter 24: TrainingChapter 25: Document reviewChapter 26: AuditsChapter 27: Management reviewChapter 28: CertificationChapter 29: Business as usualChapter 30: What to know when you are up and runningChapter 31: Conclusion