By Kimmy Ansems and Linda Giesselink, Emergo Group
Emergo by UL’s Human Factors Research and Design team has extensive experience developing software user interfaces and instructional materials for various medical devices. In the fourth blog post in our series on the European Medical Devices Regulation (MDR) and human factors engineering, we reference various MDR General Safety and Performance Requirements (GSPRs) laid out in Annex I associated with the design of user-friendly software user interfaces and informational resources.
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 DrugDeliveryBusiness.com or its employees.
