Biopharmaceutical Manufacturing, Volume 1: Regulatory processes
Language: English
Published by IOP PUBL LTD, 2021
- Hardcover
- New
Condition: New
£ 176.05
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Add to basketItem description from seller
Über den AutorSarfaraz K. Niazi is an adjunct professor at the University of Illinois and University of Houston. Prof. Niazi has established numerous consulting businesses and start-up companies within the biopharmaceutical industry.
Seller Inventory # 898571584
- Title
- Biopharmaceutical Manufacturing, Volume 1: Regulatory processes
- Author
- Niazi, Sarfaraz K.|Lokesh, Sunitha
- Publisher
- IOP PUBL LTD
- Publication year
- 2021
- Condition
- New
- Binding
- Gebunden
- Language
- English
- ISBN 10
- 0750331739
- ISBN 13
- 9780750331739
This volume covers the regulatory processes involved in producing a GMP (Good Manufacturing Practice) biopharmaceutical product for commercial distribution, including areas of current GMP, registration, and legal and ethical considerations. Emerging trends in the technology and regulatory compliance are also discussed, with advice on establishing efficient manufacturing facilities. Intended for practitioners in the commercial biopharmaceutical manufacturing industry, the text is an ideal resource for practitioners looking to develop their ability to manufacture biopharmaceutical products at a large scale.
"Synopsis" may belong to another edition of this title.
About the Author
Sunitha Lokesh is the director of biomanufacturing operations at Pharmaceutical Scientist Inc., where she leads the identification and technology development of biopharmaceutical products. She has over 10 years of experience in developing biopharmaceuticals, from the cell line to process validation.
"About the title" may belong to another edition of this title.
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