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About Jim
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Validation of Pharmaceutical Processes Greatly expanded in scope from the 1999 2nd Edition. Provides a detailed, single-source reference for designing, qualifying, calibrating, certifying, and validating systems required to prepare aseptic and non-aseptic pharmaceutical products, drug substances (synthetic & biological), packaging, analytical methods and more. Compiles compliance and regulatory principles, documentation practices, scientific approaches, and engineering concepts that can be used independently or in combination to validate products, processes, and equipment. Among the topics are facility design, monitoring non-viable particles, validating utilities, steam sterilization-in-place technology, sterilizing-grade filters, preparing components, packaging operations, and process control and quality systems. Co-editor with Frederick Carleton, Validation of Pharmaceutical Processes,
Reviews "…an excellent presentation on the subject of validation of pharmaceutical processes related to sterile products. It is written in a simple language and can be easily understood at the same time without losing the importance of the subject. The book will be an asset to education institutions in pharmacy and pharmaceutical technology, project and manufacturing personnel of sterile product manufacturing organisations and also to quality assurance and R&D personnel."—Pharmatimes James Agalloco has published a variety of other publications. If you'd like a copy of any of these papers, please send Jim an email.
Advanced Aseptic Processing Technology This book is intended to provide complete coverage of emerging aseptic processing technology, in particular those technologies that are reshaping the production of sterile healthcare products including: isolators, restricted access barrier systems, robotics, disposables and others. Use discount code AUTHOR25 to receive a 25% discount when purchasing the book. |
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