Pharmaceutical Manufacturing Handbook e-bog
2190,77 DKK
(inkl. moms 2738,46 DKK)
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 ke...
E-bog
2190,77 DKK
Forlag
Wiley-Interscience
Udgivet
4 april 2008
Genrer
Chemistry
Sprog
English
Format
pdf
Beskyttelse
LCP
ISBN
9780470259825
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.