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from C.H.I.P.S.
Two-Volume Set edited by Shayne Cox Gad
Pharmaceutical Manufacturing Handbook covers a range of topics to help professionals better understand the methods used in the pharmaceutical manufacturing, pharmaceutical engineering, and process engineering fields.
It covers many aspects, such as the building of a facility, to the various dosage and delivery forms available, and finally to the principles of validation. Other topics include quality assurance and regulatory requirements.
This work is available as a two-volume set at significant savings, see ordering details below or you can purchase the individual volumes as follows:
Volume 1: Regulations and Quality provides complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing.
Volume 2: Production and Processes covers the full range of topics to help you understand and apply the methods needed to manufacture drugs safely and efficiently.
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