The Challenge of CMC Regulatory Compliance for Biopharmaceuticals and Other Biologics 2nd ebook

Name: The Challenge of CMC Regulatory Compliance for Biopharmaceuticals and Other Biologics 2nd ebook
SKU: 258492_4548657
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$21.99

The Challenge of CMC Regulatory Compliance for Biopharmaceuticals and Other Biologics 2ndBy: John Geigert Publisher: Springer Print ISBN: 9781461469155, 1461469155 other ISBN: 9781461469162, 1461469163 Edition: 2nd Copyright year: 2013This book highlights the challenges facing quality assurance/quality control (QA/QC) in Today's biopharmaceutical environment and presents the strategic importance and value generated by QA/QC for their involvement in control of manufacturing. It will put into perspective the need for a graded approach to QA/QC from early clinical trials through market approval. Since the first edition published in 2004, there have been more than 50 new regulatory guidances released by the Food and Drug Administration (FDA), European Medicines Agency (EMA) and ICH that affect the CMC regulatory compliance of biopharmaceuticals; also the application of biosimilars has been developed in Europe and is under development in the USA. The revised update will be broadened to include not only biopharmaceuticals (biotech drugs) but also other biologics (vaccines, cell therapy, plasma-derived proteins, etc.)

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The Challenge of CMC Regulatory Compliance for Biopharmaceuticals and Other Biologics 2ndBy: John Geigert Publisher: Springer Print ISBN: 9781461469155, 1461469155 other ISBN: 9781461469162, 1461469163 Edition: 2nd Copyright year: 2013This book highlights the challenges facing quality assurance/quality control (QA/QC) in Today’s biopharmaceutical environment and presents the strategic importance and value generated by QA/QC for their involvement in control of manufacturing. It will put into perspective the need for a graded approach to QA/QC from early clinical trials through market approval. Since the first edition published in 2004, there have been more than 50 new regulatory guidances released by the Food and Drug Administration (FDA), European Medicines Agency (EMA) and ICH that affect the CMC regulatory compliance of biopharmaceuticals; also the application of biosimilars has been developed in Europe and is under development in the USA. The revised update will be broadened to include not only biopharmaceuticals (biotech drugs) but also other biologics (vaccines, cell therapy, plasma-derived proteins, etc.)