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Pharmaceutical Manufacturing Handbook

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Pharmaceutical Manufacturing Handbook

Format

Hardback

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Pharmaceutical Manufacturing Handbook
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Description

With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the book discusses quality assurance and validation, drug stability, and contamination control, all key aspects of pharmaceutical manufacturing that are heavily influenced by regulatory guidelines. The team of expert authors offer you advice based on their own firsthand experience in all phases of pharmaceutical manufacturing.

Author Biography

SHAYNE COX GAD, PhD, DABT, ATS, is the Principal of Gad Consulting Services. Dr. Gad has more than thirty years of experience as a toxicologist, statistical consultant, manager, and general consultant on research and development in the chemical, consumer product, contract testing, biotechnology, medical device, and pharmaceutical industries. He is the author of twenty-nine books and numerous papers, presentations, and other publications.
Release date NZ
March 17th, 2008
Contributor
Edited by Shayne Cox Gad
Country of Publication
United States
Imprint
Wiley-Blackwell
Pages
856
Dimensions
179x258x51
ISBN-13
9780470259597
Product ID
3089847

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