Working on a Post-Inspection FDA Response - MasterControl

July 13, 2016

After an FDA investigator has inspected your facility and issued a Form 483, it is critical to meet the post-inspection response requirements. Failure to do so can have devastating consequences. Attend this webinar for practical knowledge of what quality managers need to know to conduct CAPAs, manage resources and meet FDA response commitments.

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MasterControl eMDR™
MasterControl eMDR™

The FDA requires medical device manufacturers to report any adverse events to the agency.

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After an FDA Inspection
After an FDA Inspection

MasterControl quality and compliance expert Walt Murray presents what needs to happen in the wake of a U.S....