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HOW TO DESIGN A WORLD-CLASS Corrective Action Preventive Action SYSTEM FOR FDA-REGULATED INDUSTRIES: A HANDBOOK FOR QUALITY ENGINEERS AND QUALITY MANAGERS - Couverture souple

Muchemu, David

 
9781425950538: HOW TO DESIGN A WORLD-CLASS Corrective Action Preventive Action SYSTEM FOR FDA-REGULATED INDUSTRIES: A HANDBOOK FOR QUALITY ENGINEERS AND QUALITY MANAGERS

Synopsis

The CAPA (Corrective Action/Preventive Action) Quality subsystem is the most audited by FDA inspectors. This book is designed to help Quality management professionals in Biomedical, Pharmaceutical, Tissue, and Medical Device industries design a CAPA Quality subsystem that meets and exceeds CAPA requirements in 21CFR 820.100(J).This book accomplishes the following:· Defines CAPA· Provides cross-functional process flows· Provides requirements for a CAPA system· Provides examples for the document hierarchy needed· Provides definitions for a CAPA system· Provides examples of work instructions, and standard operating procedures for a CAPA system.

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Biographie de l'auteur

Mister Muchemu has a degree in Biology and chemistry from Warren Wilson College in North Carolina. He is an MBA with over twenty years of experience in Medical Device, Biomedical, Tissue banking, and Pharmaceutical organizations. Over the years the Mister Muchemu has worked as a Quality Engineer, Quality manager, Supplier Quality Engineer, and Change control manager. His passion is Quality management, and Quality control. Mister Muchemu career path has taken him through various Quality Control and Quality management positions in the following organizations:· Johnson and Johnson· Boston scientific· American Red cross Biomedical services· Tissue Banks international· Abbott laboratories· Applied Biosystems

Présentation de l'éditeur

The CAPA (Corrective Action/Preventive Action) Quality subsystem is the most audited by FDA inspectors. This book is designed to help Quality management professionals in Biomedical, Pharmaceutical, Tissue, and Medical Device industries design a CAPA Quality subsystem that meets and exceeds CAPA requirements in 21CFR 820.100(J).This book accomplishes the following:· Defines CAPA· Provides cross-functional process flows· Provides requirements for a CAPA system· Provides examples for the document hierarchy needed· Provides definitions for a CAPA system· Provides examples of work instructions, and standard operating procedures for a CAPA system.

Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.