Audio and Web Conference
Top 10 Health Technology Hazards 2021: An In-Depth Look at Managing Medical Devices with COVID-19 Emergency Use Authorization
Overview
Our February 17, 2021, webcast recording explores the number 1 topic on this year's Top 10 Health Technology Hazards list: Complexity of Managing Medical Devices with COVID-19 Emergency Use Authorization (EUA). Presenters discussed FDA's criteria for issuing EUAs, the temporary nature of EUA device authorization, and actionable recommendations for managing EUA devices in your facility during the COVID-19 public health emergency. Register to view the session recording, including live Q&A, plus supplementary materials.
Speakers
- Andrew Furman, MD, MMM, FACEP, Executive Director, Clinical Excellence, ECRI
- Amanada Sivek, PhD, Principal Project Officer, Device Evaluation, ECRI
- Tom Toczylowski, Assistant Director, Healthcare Product Alerts, ECRI
- Rob Schluth, Principal Project Officer, Device Evaluation, ECRI
- Jason Launders, MS, Director of Operations, Device Evaluation, ECRI
Lab tour recording
Supplementary materials
ECRI exclusive reports
- Use of Unapproved Devices or New Applications for Existing Medical Devices to Address COVID-19 Shortages without an EUA May Jeopardize Patient or Staff Safety
- Ventilators on FDA Emergency Use Authorization List: Hospitals Should Seek Clarity on post-EUA Status before Purchasing
EUA alert
The following is an example of the type of alerts ECRI will be publishing in its Health Devices Alerts database to keep members apprised of any substantial EUA changes:
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