Webinar-Validation
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Complimentary Webinar: Reducing the Validation Merry-Go-Round- Lowering the time and cost of computer system validation while ensuring FDA compliance -
Date: Wednesday 27th January 2010 Benefits from the Webinar:
Any pharmaceutical or medical device manufacturer who does not use validated software, relies on costly manual and paper processes which may compromise the safety, quality and value of its products. However, the software validation process can be extremely expensive and time consuming. Many companies employ full-time validation teams who are on a continuous global loop of validating and witnessing every computer system install and upgrade used in the production process – ‘the validation merry-go-round’. Validation establishes by objective evidence that all requirements have been implemented correctly, successfully and are traceable to systems requirements. Remember in the eyes of the regulators, if it’s not documented, then it’s just a rumor. ‘Reducing the Validation Merry-Go-Round – Lowering the time and cost of computer system validation while ensuring FDA compliance’ webinar explored how the validation merry-go-round can be dramatically reduced. In the session, Dave Taylor and Andy McLaughlin from PRISYM ID presented an in-depth look into the development of web-based labeling and management solutions which supports in meeting FDA 21 CFR Part 11, GCP, GMP and Sarbanes-Oxley regulations. Compliance can make or break you, however so can the costs involved. In a time when ‘cost is king’, one should know how to lower the time and cost of validating systems for global compliance. ( please register or login first, using the form above, to view the webinar ) For more information contact PRISYM ID Marketing at:
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View the Validation webinar recorded broadcast
