The Impact of EU MDR Implementation, and How it Will Change Your Business

When: March 10, 2020, 12:00 pm - 1:30 pm
Where: M2D2, 110 Canal Street, 4th Floor, Lowell, MA

This webinar, led by RQMIS Senior European Regulatory Consultant Dr. Maria Duguine, outlines what provisions are currently in place during the transition period for the EU Medical Device Regulations.

The transition period for the EU Medical Device Regulations (MDR) began in May 2017 and will end when they go into full force on May 26,2020. During this transition phase, a number of provisions have been put in place to assist manufacturers, but they are widely misunderstood and have caused major setbacks for companies trying to adhere to the new regulations. This webinar, led by RQMIS Senior European Regulatory Consultant Dr. Maria Duguine, outlines what provisions are currently in place during the transition period, including how to properly adhere to and implement them. We will also review what will change when the MDR goes into force on May 26th and how this could affect your business. It is imperative that manufacturers get ahead of this change before the deadline for conformity.

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