logo

EbookBell.com

Most ebook files are in PDF format, so you can easily read them using various software such as Foxit Reader or directly on the Google Chrome browser.
Some ebook files are released by publishers in other formats such as .awz, .mobi, .epub, .fb2, etc. You may need to install specific software to read these formats on mobile/PC, such as Calibre.

Please read the tutorial at this link:  https://ebookbell.com/faq 


We offer FREE conversion to the popular formats you request; however, this may take some time. Therefore, right after payment, please email us, and we will try to provide the service as quickly as possible.


For some exceptional file formats or broken links (if any), please refrain from opening any disputes. Instead, email us first, and we will try to assist within a maximum of 6 hours.

EbookBell Team

Process Validation In Manufacturing Of Biopharmaceuticals Guidelines Current Practices And Industrial Case Studies Anurag S Rathore G K Sofer

  • SKU: BELL-4343064
Process Validation In Manufacturing Of Biopharmaceuticals Guidelines Current Practices And Industrial Case Studies Anurag S Rathore G K Sofer
$ 31.00 $ 45.00 (-31%)

4.0

36 reviews

Process Validation In Manufacturing Of Biopharmaceuticals Guidelines Current Practices And Industrial Case Studies Anurag S Rathore G K Sofer instant download after payment.

Publisher: Taylor & Francis
File Extension: PDF
File size: 4.05 MB
Pages: 578
Author: Anurag S Rathore; G K Sofer
ISBN: 9781574445169, 1574445162
Language: English
Year: 2005

Product desciption

Process Validation In Manufacturing Of Biopharmaceuticals Guidelines Current Practices And Industrial Case Studies Anurag S Rathore G K Sofer by Anurag S Rathore; G K Sofer 9781574445169, 1574445162 instant download after payment.

Content: 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 ZEVALINO Purification Process - A Case Study, L. Conley, J. McPherson, and J. Thommes 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

Related Products