To successfully bring an Active Pharmaceutical Ingredient (API) to market, many steps must be followed to ensure compliance with governmental regulations. This

A guide to the development and manufacturing of pharmaceutical products written for professionals in the industry, revised second edition The revised and update

Much has happened in the area of bulk pharmaceutical good manufacturing practice (GMP) and validation since the first publication of Validation of Active Pharma

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Focusing on the three most critical components that successfully bring an API to market-process development, manufacturing, and governmental regulation and appr