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:

• Discover how web-based applications reduce the burden of validation
• Understand how to significantly reduce costs while gaining and maintaining strict compliance with regulations: FDA 21 CFR Part 11, GCP, GMP and Sarbanes-Oxley
• Answer key questions on how the differences between thin and thick client based software can affect your business when designing, producing and managing compliant labels

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 PRISYMID presented an in-depth look into the development of web-based labelling 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.

View the Validation webinar recorded broadcast (please login first, using the form above, to view the webinar )

For more information contact PRISYMID Marketing at:

info at prisymid dot com or call UK (+44)(0) 118936 4400

View the Validation webinar recorded broadcast