Risk-Based Verification and Validation to Meet FDA 820.75 and ISO 13485 Requirements Best Practices to Move from a Classic Approach to a Risk-Based Approach

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The FDA leaves it up to companies to determine the appropriate level of testing for processes, systems and software based on the definition of validation that requires “establishing by objective evidence that a process consistently produces a result or product meeting its predetermined specifications.”

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Webinar PLUS Audio CD/Transcript - April 30, 2013 Best Value! Save $147! You’ll have access to one log-in and dial-in for the live 90-minute webinar for unlimited participants. You also receive all presentation materials and the opportunity to ask question by phone and email, plus an audio CD and transcript for the entire session.
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Webinar Only - April 30, 2013 You get one log-in and dial-in for the live 90-minute webinar for unlimited participants, presentation materials and the opportunity to ask question by phone and email.
$347.00