Dr. Andrew Webster, chair and professor of pharmaceutical sciences, recently published a chapter titled “Pharmaceutical Product Stability” in the Pharmaceutical Manufacturing Handbook, Volume 2 Regulations and Quality by Wiley Publishers.With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the book discusses quality assurance and validation, drug stability, and contamination control, all key aspects of pharmaceutical manufacturing that are heavily influenced by regulatory guidelines.
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