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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 David Muchemu
How to Design a World-class Corrective Action Preventive Action System for Fda-regulated Industries: a Handbook for Quality Engineers and Quality Managers
David Muchemu
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.
| Media | Books Paperback Book (Book with soft cover and glued back) |
| Released | August 17, 2006 |
| ISBN13 | 9781425950538 |
| Publishers | AuthorHouse |
| Pages | 104 |
| Dimensions | 210 × 279 × 6 mm · 254 g |
| Language | English |