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Pharmaceutical Equipment Validation
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Pharmaceutical Equipment Validation : The Ultimate Qualification Guidebook

Book Details

Format Hardback or Cased Book
ISBN-10 1574910795
ISBN-13 9781574910797
Publisher Taylor & Francis Inc
Imprint CRC Press Inc
Country of Manufacture US
Country of Publication GB
Publication Date Aug 31st, 1998
Print length 450 Pages
Weight 1,768 grams
Dimensions 29.00 x 22.30 x 2.90 cms
Product Classification: Biology, life sciences
Ksh 42,300.00
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Comprehensively covering equipment qualification and process validation for pharmaceutical process equipment, this text shows readers how to demonstrate compliance, what data to use, and how to produce the appropriate documentation. The author demonstrates how to prepare, test, and complete equipment qualification protocols. He also explains how to perform qualification testing and whether to test the equipment for a worst-case scenario. The thirty-eight completed protocol templates cover specific equipment types, provide instant answers to most protocol writing and testing questions, show how to qualify each piece of equipment, and provide a check for readers'' own protocols.
While FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide guidelines on how to produce that documentation. Pharmaceutical Equipment Validation gives details on how to demonstrate compliance, what data to use, and how to produce the appropriate documentation. This book''s user-friendly diagrams and other clear graphics illustrate key ideas throughout each protocol, offering a bird''s-eye view of what is coming next-and they quickly guide you through the equipment validation. The author provides a thorough understanding of how to prepare, test, and complete equipment qualification protocols. He also explains how to perform qualification testing and whether to test the equipment for a worst case scenario.

No other book deals exclusively with the key issues of equipment qualification and process validation for pharmaceutical process equipment-and provides instructions on how to achieve it. With pragmatic approach, this book includes 38 useful protocol templates, already completed, that provide instant answers to most protocol writing and testing questions. These templates cover specific equipment types, such, and provide accurate, industry acceptable equipment qualification protocols. Step-by-step, they show how to qualify each piece of equipment, and they provide a check for readers own protocols.

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