Companies attempting to comply with Medical Device Regulation (EU) 2017/745 (MDR), introduced in May 2021 for medical device certification in the EU are challenged by the complexity and scope of the requirements. It is important for medical device companies to understand the latest requirements in the EU MDR, to minimize the risk of non-compliance and inability to certify products in the EU.
Register to gain a clear understanding of the essential EU MDR requirements for medical device registration and vigilance.
Speakers:
Aarekh Shrestha
Sr. Manager and Head of Drug Safety/Device Vigilance
Garima Tripathi
Sr. Drug Safety Physician