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Eliminate the Confusion ? Analytical Method Qualification and Validation
Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702314?channel=ourglocal |
Edit Freely
Category Biotech
Deadline: June 08, 2012 | Date: June 08, 2012
Venue/Country: Palo Alto, U.S.A
Updated: 2012-05-30 18:51:40 (GMT+9)
Call For Papers - CFP
This webinar will help you understand the significant differences between qualification and validation of an analytical method, the expectations and requirements of each, and their place in the analytical method lifecycle.Why Should You Attend:Execution of a method validation is a resource intensive activity, both in terms of manpower, equipment usage, time, and money. The more the process is well defined and understood, the greater the potential for an efficient project. The less the process and its elements are understood, the greater the chance for delays and additional resource expenditures.Areas Covered in the Seminar:- Definitions of Terms-qualification, validation, verification, co- validation, intended use.- Standards-Q2R1, FDA Guidelines.- Requirements for Entry-what is needed in order to start a qualification or validation.- Requirements for Execution.- Documentation needs-SOPs, Forms, Worksheets, Data Output, Protocols, Reports.- Pitfalls and potential resolutions.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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