Author: Gail Sofer
Edition: 1
Publisher: CRC Press
Binding: Hardcover
ISBN: 0824702492
Process Validation in Manufacturing of Biopharmaceuticals: Guidelines, Current Practices, and Industrial Case Studies (Biotechnology and Bioprocessing Series)
A study of biopharmaceutical process validation. Medical books Process Validation in Manufacturing of Biopharmaceuticals. It aims to enable developers and producers to ensure safe products, reduce the risk of adverse reactions in patients, and avoid recalls by outlining sophisticated validation approaches to characterize processes, process intermediates, and final product fully Medical books Process Validation In Manufacturing Of Biopharmaceuticals, Third Edition Rathore. format hardback language english publication year 01 06 2012 subject engineering technology subject 2 industrial chemistry manufacturing title process validation in manufacturing of biopharmaceuticals third edition author rathore anurag s edited by sofer gail edited by publisher crc pr i llc publication date mar 29 2012 pages 600 binding hardcover edition 3 rd dimensions 6 46 wx 9 69 hx 1 18 d isbn 1439850933 subject medical pharmacology brand new hardcover all orders get full access to our on
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format hardback language english publication year 01 06 2012 subject engineering technology subject 2 industrial chemistry manufacturing title process validation in manufacturing of biopharmaceuticals third edition author rathore anurag s edited by sofer gail edited by publisher crc pr i llc publication date mar 29 2012 pages 600 binding hardcover edition 3 rd dimensions 6 46 wx 9 69 hx 1 18 d isbn 1439850933 subject medical pharmacology brand new hardcover all orders get full access to our on
"Written by experienced authorities in process validation, Process Validation in Manufacturing of Biopharmaceuticals explores current trends in the field and strategies for the selection of the most appropriate quality control scheme. It offers practical guidelines, recommendations, and an abundance of industrial case studies that demonstrate various techniques and approaches in the validation of biopharmaceutical processes. Provides specific examples of failure modes and effect analysis (FMEA) that help you establish this method in your organizationFile Size: 5469 KBPrint Length: 600 pagesPub
"Written by experienced authorities in process validation, Process Validation in Manufacturing of Biopharmaceuticals explores current trends in the field and strategies for the selection of the most appropriate quality control scheme. It offers practical guidelines, recommendations, and an abundance of industrial case studies that demonstrate various techniques and approaches in the validation of biopharmaceutical processes. Provides specific examples of failure modes and effect analysis (FMEA) that help you establish this method in your organizationFile Size: 5469 KBPrint Length: 600 pagesPub
"Written by experienced authorities in process validation, Process Validation in Manufacturing of Biopharmaceuticals explores current trends in the field and strategies for the selection of the most appropriate quality control scheme. It offers practical guidelines, recommendations, and an abundance of industrial case studies that demonstrate various techniques and approaches in the validation of biopharmaceutical processes. Provides specific examples of failure modes and effect analysis (FMEA) that help you establish this method in your organizationFile Size: 5469 KBPrint Length: 600 pagesPub
Medical Book Process Validation in Manufacturing of Biopharmaceuticals
It aims to enable developers and producers to ensure safe products, reduce the risk of adverse reactions in patients, and avoid recalls by outlining sophisticated validation approaches to characterize processes, process intermediates, and final product fully. The text emphasizes cost effectiveness while determining what level of validation is required for different phases of development, license application, and process improvements.
