<p>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.</p>

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.

Improving Medical Device Adverse Event Reporting

Many medical devices, including surgical mesh, do not undergo the same scrutiny as prescription drugs. As a result, patients become the post-market clinical trial subjects, and many suffer devastating and permanent injuries.

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Improving Medical Device Adverse Event Reporting

Improving Medical Device Adverse Event Reporting