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Software Validation Do's and Don'ts


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Software Validation: The Do's and Don'ts

Thursday, January 20, 2011
2:00 PM to 3:00 PM EDT


Software validation is often times a very misunderstood concept.  For FDA regulated industries, there are clear expectations including “the least burdensome approach.”  Validation alone does not guarantee software quality—many other aspects of software engineering are required.
Join software expert, John Cachat, as he discusses how to solve several software validation issues, including:

  • Requirements
  • Defect Prevention
  • Time and Effort
  • Software Life Cycle
  • Plans
  • Procedures
  • Software Validation After a Change
  • Validation Coverage
  • Independence of Review
  • Flexibility of Responsibility

If you are having trouble with software validation, you cannot afford to miss this presentation.

Space is limited. Register now!

About the Presenter:
John M. Cachat has been designing, programming, implementing, validating, and maintaining software systems for over 25 years.  As a direct supplier of software to the US FDA, John will share his experience about the process and misconceptions of software validation. John has a BSIE degree from Kettering University and an MSIE degree from Texas A&M University.

This is a free Webinar.

This webinar may qualify for professional certification credit, and a certificate of participation will be distributed to all attendees.

To register: 
https://www2.gotomeeting.com/register/962835035

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