FREE REPLAY
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European regulation on Medical Devices: still not compliant?

MEDICAL DEVICES

On 26th May 2021 the new Medical Device Regulation (MDR) 2017/745 has entered into force !

From this date, only Medical Devices that are compliant with the new MDR should continue to be marketed in the European Market. 

If you still do not comply, it is urgent to start the compliance process to be able to continue to sell your devices.

Come to discover with us how to be compliant with the MDR 2017/745 !

During this webinar, we will answer the following questions :

  • What are the main requirements of the new MDR? 
  • How to successfully bring into compliance Medical Devices with the new regulation?
  • What are the risks if you still do not comply with the new regulations?
 

AGENDA

  • Presentation of the context,
  • Key points and regulatory requirements of the MDR 2017/745,
  • Risks of non-compliance.

REGISTER TO SEE THE REPLAY!

Raïssa ABDEL-KADER
Business Developer

After more than 6 years of experience as a sales representative in long sales cycles, and a double technical-commercial competence, Raïssa supports manufacturers in the compliance of their medical devices.

 
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