Handbook of Pharmaceutical Manufacturing Formulations, Third Edition (e-bog) af Niazi, Sarfaraz K.
Niazi, Sarfaraz K. (forfatter)

Handbook of Pharmaceutical Manufacturing Formulations, Third Edition e-bog

2190,77 DKK (inkl. moms 2738,46 DKK)
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Six, Sterile 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 sixth volume of a six-volume set, compiles data from FDA and EMA new drug applications, patents and patent applications, and othe...
E-bog 2190,77 DKK
Forfattere Niazi, Sarfaraz K. (forfatter)
Forlag CRC Press
Udgivet 9 december 2019
Længde 416 sider
Genrer Reference works
Sprog English
Format pdf
Beskyttelse LCP
ISBN 9781351592239
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Six, Sterile 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 sixth 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:i a a a a a a Largest source of authoritative and practical formulations, cGMP compliance guidance and self-audit suggestionsi a a a a a a Differs from other publications on formulation science in that it focuses on readily scalable commercial formulations that can be adopted for cGMP manufacturingi a a a a a a Tackles common difficulties in formulating drugs and presents details on stability testing, bioequivalence testing, and full compliance with drug product safety elementsi a a a a a a Written by a well-recognized authority on drug and dosage form development including biological drugs and alternative medicines