Improving Medical Device Adverse Event Reporting

May 20, 2021
Hosted by:
Jane Akre
Madris (Tomes) Kinard, MBA
In this program, Ms. Kinard, a former FDA Program Manager, offers an in-depth analysis of the broken medical device adverse events reporting system and how Device Events provides easier access to this critical data through clear, comprehensive, metrics, reports and signal alerts that can be used to improve health outcomes.

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