Author: Phil Cloud
Edition: 1
Publisher: CRC Press
Binding: Hardcover
ISBN: 1574910795
Pharmaceutical Equipment Validation: The Ultimate Qualification Guidebook
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. Medical books Pharmaceutical Equipment Validation. 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 Medical books Pharmaceutical Equipment Validation: The Ultimate Qualification Guidebook. Categories: Pharmaceutical technology. Contributors: Phil Cloud - Author. Format: Hardcover
Download link for Pharmaceutical Equipment Validation The Ultimate Qua..., 9781574910797
Categories: Pharmaceutical technology. Contributors: Phil Cloud - Author. Format: Hardcover
author phillip a cloud format hardback language english publication year 31 08 1998 subject family health relationships subject 2 coping with problems illness title pharmaceutical equipment validation the ultimate qualification guidebook author phil cloud publisher informa healthcare publication date aug 01 1998 pages 443 binding hardcover edition 1 st dimensions 8 50 wx 11 00 hx 1 00 d isbn 1574910795 subject medical pharmacy brand new hardcover all orders get full access to our online status
"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
"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
Medical Book Pharmaceutical Equipment Validation
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.
