Biopharmaceutical Manufacturing, Volume 1: Regulatory Processes
Niazi, Sarfaraz K., Lokesh, Sunitha
This two-volume set provides a comprehensive guide to the essential aspects of commercial biopharmaceutical manufacturing. Covering the planning, layout and operation of successful commercial manufacturing, the aim of the books is to enable innovations, new drug development, and make affordable biological drugs available to patients worldwide. 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.Key Features: Covers the essential aspects of commercial biopharmaceutical manufacturing for industry practitioners, including the planning, layout and operationProvides sufficient information for industry practitioners to establish and operate GMP (Good Manufacturing Practice) compliant manufacturing operationsIncludes case studies and step-by-step procedures for manufacturing specific biopharmaceutical productsFocused exclusively on products intended for human useIncludes coverage of regulatory requirements, intellectual property challenges, training of manufacturing teams and issues around cost optimisation
Volume:
1
Anno:
2022
Casa editrice:
Iop Publishing Ltd
Lingua:
english
Pagine:
448
ISBN 10:
0750331739
ISBN 13:
9780750331739
File:
PDF, 20.10 MB
IPFS:
,
english, 2022
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