The purpose of this handbook is to assist individuals for the Certified Pharmaceutical Good Manufacturing Practices Professional (CPGP) examination and provide a reference for the practitioner. The second edition reflects the Body of Knowledge which was updated in 2015. This edition has also incorporated additional information including updated references. The updates reflect the current trends and expectations of the evolving pharmaceutical industry driven by consumer expectations and regulatory oversight.
This handbook covers compliance with good manufacturing practices (GMPs), as regulated and guided by national and international agencies for the pharmaceutical industry. It covers finished human and veterinary drugs and biologics, and combination devices, as well as their component raw materials (including active pharmaceutical ingredients (APIs) and excipients), and packaging and labeling operations.
This handbook covers compliance with good manufacturing practices (GMPs), as regulated and guided by national and international agencies for the pharmaceutical industry. It covers finished human and veterinary drugs and biologics, and combination devices, as well as their component raw materials (including active pharmaceutical ingredients (APIs) and excipients), and packaging and labeling operations.
€149.99
About the author
Mark Allen Durivage has worked as a practitioner, educator, and consultant. He is Managing Principal Consultant at Quality Systems Compliance LLC. He is an American Society for Quality (ASQ) Fellow and holds several ASQ certifications.
Language English ● Format EPUB ● Pages 516 ● ISBN 9781951058906 ● File size 4.4 MB ● Editor Mark Allen Durivage ● Publisher ASQ Quality Press ● Published 2016 ● Edition 2 ● Downloadable 24 months ● Currency EUR ● ID 8744668 ● Copy protection Adobe DRM
Requires a DRM capable ebook reader
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