Designing A World-Class Quality Management System For FDA Regulated Industries
Quality System Requirements (QSR) For cGMP
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The QSR (Quality system Regulations) define a Quality Management system as follows:
“The organizational structure, responsibilities, processes, procedures, and resources for implementing quality management”
Source: 21CFR820.39 (v)
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About the Book
Having a robust and functional Quality Management system is a QSR requirement for all Pharmaceutical,Biomedical,and Medical Device companies.This book does the following for you:
1.It helps Managers in Startup companies design a Quality management system that meets and exceeds QSR requirements.
2.It helps you understand requirements for the design of a Quality Management system for Medical Device,Pharmaceutical,Tissue,and Biomedical industries
3.It provides the Quality system document structure
4.It helps you understand Quality system requirements for ISO 13485,and ISO 9001
5.It provides standard definitions for the Quality management system
6.It provides examples of Quality system related warning letters written by the FDA during onsite audits
7.It provides the reader several models of a Quality Management system
About the Author
David N.Muchemu is the author of "How to Design A World-Class Corrective Action and Preventive Action System for FDA regulated industries",and "Change Control for FDA Regulated Industries".Mr Muchemu has extensive experience in Pharmaceutical,Medical Device,Biomedical,and Tissue Industries.He has worked in different capacities at Boston Scientific,Johnson and Johnson,American Redcross Biomedical services,Guidant,Advanced Bionics , Applied Biosystems and Tissue Banks International.He is the founder of QSi (LLC),a Quality Management System/cGMP consulting firm in San Jose,California.