Pharmaceutical Vendors Approval Manual

A Comprehensive Quality Manual for API and Packaging Material Approval

This book provides stepwise guidance on how to evaluate, audit, qualify and approve an active pharmaceutical ingredient (API) and packaging material manufacturer and supplier to enhance the GMP within the industry. The book will also be beneficial for institutions conducting pharmaceutical technology courses in terms of GMP and GLP applications.

janvier 2024, env. 152 pages, Anglais
Taylor and Francis
978-1-03-203813-1

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