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FDA VALIDATION 2011 - Reduce COTS Software Validation using the risk-based approach
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701583?channel=ourglocal |
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Category COTS Software Validation; Computer System Validation; Validation Documentation; FDA requirements for software validation
Deadline: October 26, 2011 | Date: October 26, 2011
Venue/Country: Palo Alto, U.S.A
Updated: 2011-10-04 15:28:02 (GMT+9)
Call For Papers - CFP
Understand 10 step Risk based approach to validation, explore methods to decrease resource requirements and make documentation more manageable and understandable.
Why Should You Attend:This session explores proven techniques that reduce validation project time, often to one-third. Learn efficient documentation strategies for computer system validation and how to increase overall system productivity. The 10-step risk-based validation approach is detailed so that the specific documents for a validation project are understood. Explore methods to decrease resource requirements, and make documentation more manageable and understandable. This often results in a savings of two-thirds the cost. Additionally, this course will help companies increase compliance and demonstrate how to use risk management to improve system performance and promote process improvement.
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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