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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products

  May 01, 2013  
Center for Professional Innovation & Education, Inc., King of Prussia, PA
Oct. 29 & 30, 2013

Complex processes yielding complex products such as biologics and biopharmaceuticals demand numerous, non-compendial, and sometimes complex QC test methods to confirm manufacturing consistency and product quality.  This course provides a comprehensive overview of the international regulatory authority requirements and expectations for test method validation of these assays.  This course will prepare attendees with the knowledge and tools to plan and execute test method validation packages for the NDA, BLA and MAA market application dossiers, covering in-process, release and stability assays commonly used by QC in biologic and biopharmaceutical companies.  The course will cover validation of QC analytical test methods (e.g., electrophoretic, HPLC, peptide mapping, etc.), cell-based potency bioassays, immunochemical binding impurity assays and adventitious agent assays.
Organized by: Center for Professional Innovation & Education
Invited Speakers: Contact info@cfpie.com for a list of course instructors
Deadline for Abstracts: n/a
Registration: http://www.cfpie.com/showitem.aspx?productid=096&source=hummolgen
E-mail: info@cfpie.com
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