Guidance on Authorized Representatives Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR)
Insights
Dive Into Our Latest s
Guidance on Authorized Representatives Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR)
By Jill Fox
June 28, 2024
SHARE
Let's Build a Healthier
& Safer World, Together
Connect with ClinChoice to discover how we can support the
development and commercialization of your drug or device.