Dear Shimmer Users, We are planning to use Shimmer sensors for data collection in an intensive care unit as part of a research study. The Shimmer sensors are considered investigational devices in the US and they come with a number of warnings in the manual (e.g., risk of electrical shock, risk of sustaining burn as a result of failure etc.).
I am trying to reach researchers who have used Shimmer in a clinical setting and specifically ask them regarding the way they dealt with patient consent forms in light of the warnings that are listed in the manual. Thank you. Best, Behnood -- Behnood Gholami, Ph.D. Co-Founder and Chief Technology Officer AreteX Engineering Phone: (404) 654-3445
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