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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition : Volume Three, Liquid Products

Book Details

Format Paperback / Softback
ISBN-10 1032920181
ISBN-13 9781032920184
Publisher Taylor & Francis Ltd
Imprint CRC Press
Country of Manufacture GB
Country of Publication GB
Publication Date Oct 14th, 2024
Print length 456 Pages
Weight 1,072 grams
Dimensions 20.90 x 28.00 x 3.20 cms
Ksh 9,700.00
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The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Three, Liquid 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 Three, Liquid 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 third 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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