£95.00

The Challenge of CMC Regulatory Compliance for Biopharmaceuticals

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Last 374 days • 374 data points (No recent data available)

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£149.99 £85.61 £99.65 £113.70 £127.75 £141.80 £155.84 01 December 2024 04 March 2025 05 June 2025 06 September 2025 09 December 2025

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8 days 10 days 275 days · current 4 days 65 days 3 days 9 days 0 69 138 206 275 £91 £93 £95 £97 £98 £119 £150 Days at Price

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Most common price: £95 (275 days, 73.5%)

Price range: £91 - £150

Price levels: 7 different prices over 374 days

Description

Each year for the past three years, there have been about 50 new molecular medicines approved by the United States Food & Drug Administration (FDA), of which approximately 25% were new biopharmaceuticals. Over 200 recombinant proteins, monoclonal antibodies, antibody drug conjugates, fusion proteins, and Fab fragments are now in the marketplace in both the United States of America (USA) and European Union (EU). There are also now over 60 biosimilars available for all major classes of recombinant proteins and monoclonal antibodies. In addition, gene therapies using genetically engineered viruses and genetically engineered cells are now in the marketplace, and continually growing. This degree of change is reflected in the over 400 CMC regulatory compliance references listed in this book that were either issued or updated since the release of the third edition. Deficiencies in biopharmaceutical CMC regulatory compliance rarely result in termination of a product, but incan readily cause months if not years of delay in initiating clinical trials, or advancing clinical development stages, or even market approval. In summary, this book: Updates real-world CMC deficiency examples with current examples; Addresses current FDA and EMA requirements and expectations for CMC regulatory compliance; Now includes CMC regulatory compliance for the new gene-based biopharmaceuticals.

Product Specifications

Format
hardcover
Domain
Amazon UK
Release Date
16 June 2023
Listed Since
28 March 2023

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