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BIOTECH WEBINAR 2010 - Important requirements when validating sterilizing grade filters - Biotech Webinar By ComplianceOnline.
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701110?channel=ourglocal |
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Category Biotech Webinar ,sterilizing grade filter,compliance webinar.
Deadline: December 02, 2010 | Date: December 02, 2010
Venue/Country: Palo Alto, U.S.A
Updated: 2010-11-17 16:04:57 (GMT+9)
Call For Papers - CFP
This sterilizing grade filter validation training will provide valuable assistance in validating sterilizing grade liquid filters within the pharmaceutical and biotech processes.Why Should You Attend:Sterilizing grade membrane filters are used in many applications within the biopharmaceutical industry, most critically though as a point-of-use filter before the filling process. These filters require appropriate process validation to verify the filter performs as specified, for example retaining microbial contaminants and/or avoiding release of leachables or particulates.In this webinar multiple validation process steps will be described and discussed in regard to methodology and criticality. These validation processes include, viability, product bacteria challenge testing, extractable/leachables testing, unspecific adsorption, particle release, chemical compatibility and product wet integrity testing.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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