In The Press

What happens after the IVDR Implementation Date?

To discuss the much anticipated date of application for the  IVDR one of our Consultants, Colm O'Rourke, sat at down with Monir at Easy Medical Device to discuss what the DOA means for manufacturers and Notified Bodies.

The EU IVDR Guidebook and what you need to know about the regulation

In anticipation of EU IVDR’s 26 May 2022 date of application (DOA) deadline, Meddev's Regulatory CoE Rod Beuzeval  joined RAPS senior editor, publications Gloria Hall, to offer advice on what the DOA really means for companies working with IVDRs and what they can do to comply with the new regulation. 

Key mistakes to avoid in your Training Process [ISO 13485]

Meddev discusses how to avoid non-conformances in your training process with Easy Medical Device. Meddev’s Training CoE Lead, Katie Cooney and Regulatory CoE Lead, Rod Beuzeval, discuss with Monir El Azzouzi at Easy Medical Device what makes a compliant training process and the key mistakes to avoid.