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PHARMACEUTICALS 2011 - QbD Approach to Analytical Method Lifecycle - Webinar By ComplianceOnline
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701915?channel=ourglocal |
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Category Pharmaceuticals,conference,event,Webinar
Deadline: March 29, 2011 | Date: March 29, 2011
Venue/Country: Palo Alto, U.S.A
Updated: 2011-02-14 18:12:56 (GMT+9)
Call For Papers - CFP
Why Should You Attend:Analytical methods play a key role in assuring that drug substances and drug products conform to their specifications. Demonstrating that these methods consistently perform appropriately for their intended purpose can be both challenging and resource intensive. By using a pro-active, quality-by-design (QbD) approach, it is possible to design better methods, understand the strengths, weaknesses and capabilities of those method and to perform validation exercises in a scientifically rational way that will maximize success and minimize overall resource consumption. This is especially true for the method transfer process, where many examples of tremendous complication can be cited due to inadequacy in method design and development, and due to inappropriate design of method transfer protocols.NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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