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Medical Device Regulatory Market Access in Times of National Emergency

Webinar on how to submit an Emergency Use Authorization (EUA) request to manufacture critically needed medical devices

Medical Device Regulatory Market Access
THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.

How to submit an Emergency Use Authorization (EUA) request to manufacture critically needed medical devices?

This webinar was delivered on March 31, 2020 hosted by the Illinois University Incubator Network (IUIN) and led by UL experts, this webinar covers how to get critical products to market, as well as:

  • Clinical and other QMS documentation (Emergo by UL)
  • Human Factors concerns (Emergo by UL)
  • Applicable standards (UL)
  • Applicable certifications (UL)
  • Cybersecurity (UL)