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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition : Volume Four, Semisolid Products

Book Details

Format Hardback or Cased Book
ISBN-10 1138103306
ISBN-13 9781138103306
Publisher Taylor & Francis Ltd
Imprint CRC Press
Country of Manufacture GB
Country of Publication GB
Publication Date Dec 17th, 2019
Print length 502 Pages
Weight 1,476 grams
Dimensions 22.20 x 28.60 x 3.80 cms
Ksh 44,100.00
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The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing.

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this fourth volume of a six-volume set, compiles data from FDA and EMA new drug applications, patents and patent applications, and other sources of generic and proprietary formulations including author’s own experience, to cover the broad spectrum of cGMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent.

Features:

       Largest source of authoritative and practical formulations, cGMP compliance guidance and self-audit suggestions

       Differs from other publications on formulation science in that it focuses on readily scalable commercial formulations that can be adopted for cGMP manufacturing

       Tackles common difficulties in formulating drugs and presents details on stability testing, bioequivalence testing, and full compliance with drug product safety elements

       Written by a well-recognized authority on drug and dosage form development including biological drugs and alternative medicines


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