Handbook of Pharmaceutical Manufacturing Formulations: Liquid Products

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Informa Healthcare, 2009 - Medical - 400 pages
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While liquid drugs do not share the compression problems of solid dosage forms, the filling problems of powder dosage forms, or the consistency problems of semisolid dosage forms, they do have their own set of considerations in the formulation and manufacturing stages.

Highlights from Liquid Products, Volume Three include:

  • practical details involved in complying with the current good manufacturing practice requirements in liquid manufacturing
  • access to what an FDA auditor would be looking for during a liquid manufacturing audit
  • issues that may arise during a US FDA inspection
  • the protocols used for stability testing for new drugs and new dosage forms, drawn from the most current ICH guidelines

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About the author (2009)

Pakistani doctor Sarfaraz K. Niazi has been teaching in the field of pharmaceutical sciences for over 34 years. He has published over 100 research articles and over a dozen major books including textbooks and a book on patent filing. He is the recipient of several research recognition awards. He is a licensed practitioner of patent law in the United States and serves the global pharmaceutical and biotechnology industry in the transition of research ideas into useful technology. Niazi holds several major US and worldwide patents for his inventions and writes in the fields of philosophy, sociology, rhetoric and poetry. He is the author of the first book on clinical pharmacokinetics and the largest work on pharmaceutical manufacturing formulations and also on the manufacturing of therapeutic proteins. He holds several fellowship of learned societies and is a reviewer for scientific journals. He writes poetry in several languages and as a hobby translates ancient Urdu and Persian poetry into English.

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