HOW TO DESIGN A WORLD-CLASS Corrective Action Preventive

Description Specifications
Description
HOW TO DESIGN A WORLD-CLASS Corrective Action Preventive Action SYSTEM FOR FDA-REGULATED INDUSTRIES: A HANDBOOK FOR QUALITY ENGINEERS AND QUALITY MANAGERS
- Used Book in Good Condition
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:Â· Defines CAPAÂ· Provides cross-functional process flowsÂ· Provides requirements for a CAPA systemÂ· Provides examples for the document hierarchy neededÂ· Provides definitions for a CAPA systemÂ· Provides examples of work instructions, and standard operating procedures for a CAPA system.
Specifications
Country USA
Brand Authorhouse
Manufacturer AuthorHouse
Binding Paperback
UnitCount 1
EANs 9781425950538
ReleaseDate 0000-00-00

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