FREE WEBINAR
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MEDICAL DEVICES

GETTING READY FOR MAY 2020

WHEN?

📅 Thursday 2nd April 2020
🕚 2 pm - 2:30 pm (CET)

 

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MEDICAL DEVICES: WHAT'S NEW IN MAY

Until now, the medical device market was regulated by European directives. The transposition of these directives according to the legislation of each country was mandatory but left some freedom of interpretation
 
In May 2017, a European regulation was published with the aim of harmonizing the different legislations for the marketing of medical devices. It will come into force in May 2020. It results in an increase in the number of products covered and the modification of classes for some Medical Devices already certified.
 
The classification step is crucial. Indeed, it will determine the process to follow for obtaining the CE certificate. 
 
What are the main regulatory developments? What are the steps for obtaining the CE marking?

AGENDA

  • New Regulation for Medical Devices
  • Classification and Certification of a MD
  • Case study

REGISTER NOW!

Cornélia GARAUDEL
Sales representative - Cosmetics & Medical Devices

After some time spent as Formulation Development Officer and Biology & Formulation Engineer, Cornélia joined EcoMundo’s teams in Paris as a Sales Representative. She specialises in the cosmetics and medical devices industries.
 
© EcoMundo 2020
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