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Основной контент книги Pharmaceutical Manufacturing Handbook
Text PDF

Volume 857 pages

0+

Pharmaceutical Manufacturing Handbook

Regulations and Quality
Read only on Litres

This book cannot be downloaded as a file but can be read in our app or online on the website.

$282

About the book

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.

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Age restriction:
0+
Release date on Litres:
20 August 2019
Volume:
857 p.
ISBN:
9780470259825
Total size:
8.5 МБ
Total number of pages:
857
Copyright Holder::
John Wiley & Sons Limited