Process Validation in Manufacturing of Biopharmaceuticals: Guidelines, Current Practices, and Industrial Case Studies - Rilegato

Rilegato

ISBN 10: 1574445162 ISBN 13: 9781574445169

Casa editrice: CRC Press, 2005

Riassunto

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 organization

Su questo libro

Contenuti

Guidelines to Process Validation, G. Sofer
Applications of Failure Modes and Effects Analysis to Biotechnology Manufacturing Processes, R.J. Seely and J. Haury
Process Characterization, J.E. Seely
Scale-Down Models for Purification Processes: Approaches and Applications, R. Godavarti, J. Petrone, J. Robinson, R. Wright, and B.D. Kelley
Adventitious Agents: Concerns and Testing for Biopharmaceuticals, R. Nims, E. Presente, G. Sofer, C. Phillips, and A. Chang
Life Span Studies for Chromatography and Filtration Media, A.S. Rathore and G. Sofer
Validation of a Flitration Strap, J. Campbell
Analytical Test Methods for Well-Characterized Biological and Biotechnological Products, N. Ritter and J. McEntire
Facility Design Issues-A Regulatory Perspective, N. Roscioli and S. Vargo
Validation of Computerized Systems, M.J. Cahilly
Process Optimization and Characterization Studies for Purification of an E. coli-Expressed Protein Product, A.S. Rathore
Validation of the ZEVALINÒ Purification Process - A Case Study, L. Conley, J. McPherson, and J. Thömmes
Process Validation of a Multivalent Bacterial Vaccine: A Novel Matrix Approach, N.S. Pujar, M.G. Gayton, W.K. Herber, C. Abeygunawardana, M.L. Dekleva, P.K. Yegneswaran, and A.L. Lee
Viral Clearance Validation: A Case Study, M. Rubino, M. Bailey, J. Baker, J.A. Boose, L. Metzka, V. Moore, M. Quertinmont, and W. Wiler

about the editors...

ANURAG S. RATHORE is a Scientist in Process Development, Amgen Inc., Thousand Oaks, California. His group is responsible for the support of process development, process characterization, scale-up, production, and process validation of late stage products. Before joining Amgen Inc., he held a similar position at Pharmacia Corporation. Dr. Rathore has authored more than 50 publications and presentations and is series editor of the Biotechnology and Bioprocessing series for Marcel Dekker. He is the editor of several recent books including Scale-up

Dettagli dell'edizione

• Editore: CRC Press
• Data di pubblicazione: 2005
• Lingua: Inglese
• ISBN 10: 1574445162
• ISBN 13: 9781574445169
• Rilegatura: Copertina rigida
• Numero edizione: 2
• Numero di pagine: 600
• Redattore: Sofer Gail
• Contatto del produttore: non disponibile
• Persona responsabile: Buchpark GmbH; gpsr@buchpark.de; ; Krügerweg 1; Trebbin; Brandenburg; 14959; Germania