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Two human factors researchers wearing surgical masks observe a human factors study of a medical device occurring in an observation room.
Conducting Safe In-person Testing During COVID-19
The experts from Emergo by UL’s Human Factors Research & Design (HFR&D) team will share insights learned from creating a safe setting to
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Medical Device Regulatory Market Access in Times of a National Emergency
Hosted by the University of Illinois, this special webinar was developed to explain what non-medical manufacturers need to know to help alleviate
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FDA and Medical Device Emergency Use Authorization (EUA)
In January 2017, FDA issued a guidance document regarding issuance of EUAs during declared public health emergencies. This guidance provides general
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