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New guidance document for notified bodies in the EU
MedTech Summit 2020 | EU Medical Device Regulation, Notified Body Overview and Update from BSI
UDI requirements for medical device manufacturers in the EU
How to Deal With the New Post-Market Surveillance Requirements Under Regulation (EU) 2017/745
How to find a Notified Body for EU MDR or IVDR
Short course on the Medical Device Regulation (EU) 2017/745
MDCG issued guidance for classifying medical devices
Don’t Have a Coronary... make the EU Regulatory Process work for you! (Cardiovascular Devices)
What is the difference between MEDDEV and MDCG?
Notified Body overview
European and national implementation of the IVDR
Regulatory Update Outlook - Time Extension Deadline and MDCG 2022-11 Rev1
