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Strategic Selection and Development of Immunogenicity Binding Methods
Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702328?channel=ourglocal |
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Category Biotech
Deadline: July 26, 2012 | Date: July 26, 2012
Venue/Country: Palo Alto, U.S.A
Updated: 2012-05-30 18:58:32 (GMT+9)
Call For Papers - CFP
This 90-minute webinar will show how to select the best technology and format combination to develop a compliant immunogenicity binding method, and provide a check-list that itemizes all the requirements to develop a compliant validation protocol.Why Should You Attend:The principal components of a meaningful immunogenicity program consist of an initial binding screen followed by confirmation and quantitation of the positive samples.This 90-minute webinar first reviews the technologies and formats currently in use to detect unwanted immunogenicity.Areas Covered in the Seminar:- Regulatory expectations- Technology platforms: Label dependent and label independent Feasibility and timeline- Assay formats: Bridging and direct- Controls and reagents: Preparation, storage and stability- Feasibility Storage of cell banks to certify stability- Optimization: MFAT/DOE versus OFAT- Pre-validation- Check-list for validationKeywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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