CONTINUOUS MANUFACTURING IN SECONDARY PRODUCTION

Author:

Warman Martin1

Affiliation:

1. Martin Warman Consultancy Ltd; Chestfield UK

Publisher

John Wiley & Sons, Inc.

Reference31 articles.

1. Kossik , J. 2002 Think small: pharmaceutical facility could boost capacity and slash costs by trading in certain batch operations for continuous versions Pharmamag.com

2. Abboud , L. Hensley , S. 2003 Factory shift: new prescription for drug makers: update the plants; After years of neglect, industry focuses on manufacturing; FDA acts as a catalyst; The three-story blender Wall Street Journal (Eastern edition)

3. US Food and Drug Administration, Center for Drug Evaluation and Research 2003 Guidance for industry PAT: a framework for innovative pharmaceutical manufacturing and quality assurance https://www.fda.gov/downloads/drugs/guidances/ucm070305.pdf

4. US Food and Drug Administration, Center for Drug Evaluation and Research 2004 Pharmaceutical cGMPS for the 21st Century: a risk-based approach. Second progress report and implementation plan https://www.fda.gov/downloads/drugs/developmentapprovalprocess/manufacturing/questionsandanswersoncurrentgoodmanufacturingpracticescgmpfordrugs/ucm176374.pdf

5. Modernizing pharmaceutical manufacturing: from batch to continuous production;Lee;Journal of Pharmaceutical Innovation,2015

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