Webinar: Prepare for an FDA Medical Device Inspection Using the AAMI Quality System Compendium (Four-Part Series)

March 21, 2017

This two-part virtual class will provide hands-on coverage for medical device professionals on the use of the comprehensive Regulatory Requirements and Industry Practices information contained in The Quality System Compendium: CGMP Requirements and Industry Practice, Third Edition to successfully prepare for and address FDA inspectional objectives as documented in Quality System Inspection Technique (QSIT). We'll cover all aspects of QSIT and highlight specific sections of the Quality System Compendium that can be used to best prepare for a successful FDA inspection.

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