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.

TORONTO (PRWEB)
February 22, 2023

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.

Join Aarekh Shrestha, Sr. Manager and Head of Drug Safety/Device Vigilance, Veranex DM&A; and Garima Tripathi, Sr. Drug Safety Physician, Veranex, for the live webinar on Tuesday, March 14, 2023, at 2pm GMT (3pm CET/EU-Central).

For more information, or to register for this event, visit EU MDR: Compliance Requirements From the Pharmacovigilance and Vigilance Perspective.

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