European Union In-Vitro Diagnostic Device Regulation (IVDR)

On-Demand2 hours

Course Overview

This two-hour course provides comprehensive instruction on the EU In Vitro Diagnostic Device Regulation. It covers all aspects of the regulation and identifies key topics and changes, including the economic operators and new roles associated with EU IVDR, standard requirements that must be met by all IVD manufacturers, and pre- and post-market requirements of conformity assessment.

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