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Often considered a necessary evil by the pharmaceutical industry, validation is still understood by many as unrestrained bureaucracy, paperwork, and procedures whose roots and logic are obscure and only serve to slow down progress. Thoroughly defining the philosophy, application, and processes, Facility Validation: Theory, Practice, and Tools explores the validation issues relevant to the start-up of a new or upgraded manufacturing facility. The author describes policies, guidelines, and regulations relating to GMPs in the pharmaceutical industry and explores the relationship between these GMPs and the validation process. He outlines the theory and clarifies the philosophy and key principles of validation such as life-cycle approach and qualification practices. The book includes coverage of common pitfalls and how to avoid them, the difficulties and constraints a validation team has to manage, and the dangers of not adopting and following the recommended best practices. Facility validation has, in fact, become good business. It can be a tool for enhancing reliability, cost, and quality. This book makes the case that design, engineering, commissioning, and validation activities can be integrated and streamlined to accelerate a pharmaceutical manufacturing plant start-up effort, and demonstrates how to use best practices to achieve the results you desire in your organization.
About the Author: Graham C. Wrigley
Title: Facility Validation : Theory, Practice, and ...
Publisher: CRC Press
Publication Date: 2004
Binding: Hardcover
Condition: As New
Seller: Books Puddle, New York, NY, U.S.A.
Condition: New. pp. 160 1st Edition. Seller Inventory # 26542582
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Hardcover. Condition: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book. Seller Inventory # ERICA75808493234015
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Condition: New. Print on Demand pp. 160 Illus. This item is printed on demand. Seller Inventory # 8386729
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Condition: New. PRINT ON DEMAND pp. 160. Seller Inventory # 18542588
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