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Points to Consider for Cleaning Validation

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BethesdaTowers4350EastWestHighwaySuite20 0Bethesda, MD20814USATel:1 (301)656-5900Fax:1 Report No. 29 (Revised 2012) Points to Consider for Cleaning ValidationParadigm Change in Manufacturing Task Force on Technical Report No. 29 (Revised 2012): Points to Consider for Cleaning ValidationAuthorsDestin A. LeBlanc, Cleaning Validation Technologies (Chair)Gretchen Allison, PfizerJennifer L. Carlson, GenentechKoshy George, ConsultantIgor Gorsky, ConcordiaValSourceIrwin S. Hirsh, Novo Nordisk ASJamie Osborne, Siegfried (USA), Randall, Baxter BiosciencePierre-Michel Riss, Eli LillyGeorge Verghese, STERIS CorporationJenn Walsh, Bristol-Myers SquibbVivienne Yankah, Sanofi-Pasteur, content and views expressed in this Technical Report are the result of a consensus achieved by the authorizing Task Force and are not necessarily views of the organizations they to Consider for Cleaning Validation Technical Report No.

ments and /or training events in order to assist pharmaceutical manufacturers of Investigational Medicinal Products (IMPs) and commercial products in implementing the ICH guidelines on Phar- ... 9.1 Cleaning Validation Master Plans ..... 69 9.1.1 Elements of a Comprehensive Plan.... 70. 9.1.2 Harmonization of Site Cleaning ...

  Pharmaceutical, Validation, Cleaning, Cleaning validation

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