Основной контент книги Pharmaceutical Manufacturing Handbook
Text PDF
Volume 857 pages
$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 2019Volume:
857 p. ISBN:
9780470259825Total size:
8.5 МБTotal number of pages:
857Copyright holder:
John Wiley & Sons Limited