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!
Fundamentals of the EU Medical Device Regulation (MDR)
- What is MDR?
- Why was it implemented?
- When did it come to force and what are the transition timelines?
Topics:
- 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
In-person participants:
GCP-Service International HQ office, Bremen, Germany
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