White paper: The New EU MDR: Practical Implications for Manufacturers

This white paper was updated July 2020 to reflect the one-year extension to the Date of Application (DoA) for the European Union’s Medical Device Regulation (EU MDR), due to the COVID-19 pandemic.

Many medical device manufacturers are fully immersed in the transition to MDR, but with lingering MDD certifications expiring in 2024, it’s time for anyone who has put it on the back burner to engage in the process in earnest.

This white paper covers:

  • Significant changes in the MDR and implications for manufacturers
  • Important practicalities of implementation, including the limited capacity of notified bodies
  • Steps manufacturers should take now
  • A programmatic approach to compliance you can adapt for your organization

Manufacturers with medical devices of all classes can benefit from the information and strategies outlined in this paper. Fill out the form to download your copy today.

Fill out the form to download the white paper