Modernizing Pharmaceutical Manufacturing: from Batch to Continuous Production

Author:

Lee Sau L.,O’Connor Thomas F.,Yang Xiaochuan,Cruz Celia N.,Chatterjee Sharmista,Madurawe Rapti D.,Moore Christine M. V.,Yu Lawrence X.,Woodcock Janet

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmaceutical Science

Reference44 articles.

1. U.S. Pharmaceutical CGMPs for the 21st Century - A Risk-Based Approach. Maryland: Food and Drug Administration; 2004.

2. Myerson AS, Krumme M, Nasr M, Thomas H, Braatz RD. Control systems engineering in continuous pharmaceutical manufacturing May 20–21, 2014 continuous manufacturing symposium. J Pharm Sci. 2014. doi: 10.1002/jps.24311 .

3. 3. D. Throckmorton. Statement to the House of Representatives, Subcommittee on Health, Committee on Energy & Commerce “Examining Drug Shortages and Recent Effort to Address Them”. 2014 Feburary 10.

4. Felder RM, Rousseau RW. Elementary principles of chemical processes. US: Wiley; 2005.

5. Allison G, Cain YT, Cooney C, Garcia T, Bizjak TG, Holte O, et al. Regulatory and quality considerations for continuous manufacturing. May 20–21, 2014 continuous manufacturing symposium. J Pharm Sci. 2015. doi: 10.1002/jps.24324 .

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