Aseptic pharmaceutical manufacturing II
By: Groves, Michale J.
Contributor(s): Murty, Ram.
Publisher: New Delhi CRC Press 2009Edition: 1st.Description: 520, 23.6*15.8 Pages | Binding - Paperback |.ISBN: 978-0-9351-8477-5.Subject(s): PHARMACEUTICSDDC classification: 615 Online resources: Click here to access online Summary: Asceptic Pharmaceutical Manufacturing II explores the sophisticated technology, developments, and applications that allow aseptic processing to approach the sterility levels achieved with terminal sterilization. Written by experts in sterile manufacturing, this book covers aseptic technology, developments, and applications and makes a valuable contribution to understanding the issues involved in aseptic manufacture. Topics include the processing of biopharmaceuticals, lyophilization, personnel training, radiopharmaceuticals, hydrogen peroxide vapor sterilization, regulatory requirements, validation, and quality systems.Item type | Current location | Collection | Call number | Status | Date due | Barcode | Item holds |
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Text Books | School of Pharmacy Reference Section | Reference | 615 GRO/MUR (Browse shelf) | Not For Loan | B0613 |
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615 GHO Handbook of pharmaceutical technology | 615 GHO Industrial pharmacy - I | 615 GHO/DUB Basic concept in pharmacutical research | 615 GRO/MUR Aseptic pharmaceutical manufacturing II | 615 GUP Introduction to pharmaceutics-1 | 615 GUP Handbook of health education and community pharmacy | 615 GUP Pharmaceutics - I |
Asceptic Pharmaceutical Manufacturing II explores the sophisticated technology, developments, and applications that allow aseptic processing to approach the sterility levels achieved with terminal sterilization. Written by experts in sterile manufacturing, this book covers aseptic technology, developments, and applications and makes a valuable contribution to understanding the issues involved in aseptic manufacture. Topics include the processing of biopharmaceuticals, lyophilization, personnel training, radiopharmaceuticals, hydrogen peroxide vapor sterilization, regulatory requirements, validation, and quality systems.
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