Training courses:Medical Devices

Our in-depth medical device regulation training is designed to prepare pharmaceutical professionals for the new challenges presented by this evolving field.

Remaining compliant with the new Medical Device Regulation (EU) 2017/745 (MDR), presents many new challenges for medical device manufacturers, distributors and regulatory teams.  Understanding and applying the new requirements is critical for maintaining regulatory compliance, ensuring patient safety and achieving market access across Europe.

We offer in-depth MDR training designed to prepare delegates for these challenges and transition smoothly to the new Medical Device Regulation. Our medical device regulatory training offers the opportunity to the learn how to interpret and navigate the new regulation, determine device classification, understand device conformity assessment routes and implement practical compliance strategies effectively.