Following Emergo by UL’s recent webinar on the European Union’s General Data Protection Regulation (GDPR) and human factors studies for medical devices, we examine key GDPR compliance issues human factors researchers must address to avoid steep penalties. The webinar was presented by Allison Strochlic and Alexandria Trombley, Research Director and Human Factors Specialist, respectively, at Emergo by UL’s Human Factors Research & Design (HFR&D) division, as well as two legal experts from Sidley Austin, Geraldine Scali and Kate Heinzelman.
Get the full story here at the Emergo Group’s blog.
The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.
The post How medical device human factors researchers can ensure GDPR compliance appeared first on MassDevice.
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