Free Hybrid Webinar

Roadblocks to Progress: Unraveling the Strain of the EU Medical Device Regulation on Manufacturers.

Discover insights, strategies, and solutions to navigate the complex landscape of EU MDR. Engage with industry experts both in-person and virtually, as we decode challenges and pave the way for success. Secure your spot today!

(In-person participants: Arrive 15 mins early & stay for a 1-hour engaging discussion!)

Free Hybrid Webinar

Roadblocks to Progress: Unraveling the Strain of the EU Medical Device Regulation on Manufacturers.

(In-person participants: Arrive 15 mins early & stay for a 1-hour engaging discussion!)

Free Hybrid Webinar

Roadblocks to Progress: Unraveling the Strain of the EU Medical Device Regulation on Manufacturers.

(In-person participants:

GCP-Service International HQ office, Bremen, Germany

Arrive 15 mins early & stay for a 1-hour engaging discussion!)

Key takeaways

Join us in-person, or via Zoom as we unravel the topics below:

What is MDR?
Why was it implemented?
When did it come to force and what are the transition timelines?

An overview of the challenges for manufacturers
Increased scrutiny for pre-market approval
The impact on small and medium sized enterprises (SMEs)
Solutions to navigate the new MDR requirements.
Conclusion and our recommendations

Join us in-person, or via Zoom as we unravel the topics below:

What is MDR?
Why was it implemented?
When did it come to force and what are the transition timelines?

An overview of the challenges for manufacturers
Increased scrutiny for pre-market approval
The impact on small and medium sized enterprises (SMEs)
Solutions to navigate the new MDR requirements.
Conclusion and our recommendations

Audience

This webinar is directed towards:

Designed for professionals in the medical device industry.

Abstract:

Whether you’re a medical device manufacturer, distributor, or regulatory professional, don’t let the EU Medical Device Regulation (MDR) catch you off guard! Join our exclusive hybrid event and gain expert insights on the fundamentals of MDR, covering everything from its definition to the reasons behind its implementation. Discover the timeline for compliance and transition and learn how to navigate the challenges posed by this vital regulation.