The evolution of the regulatory framework of MDs in Europe
The regulatory panorama of medical devices is changing according to the need of new laws disciplining this growing innovative field and the new European Regulation on medical devices which is mandatorily applied by the manufacturers from the 26th of May 2021.
The webinar “The evolution of the regulatory framework of MDs in Europe” will deepen in the general aspects on medical devices, absorption issues, the new requirements and changes compared to the older one and which are the specific needs to be covered according to the MDs Regulation to develop safer and adequate MDs for paediatric patients.
The webinar will take place on the 28th of October 2021 at 15.00 CEST and it will last an hour with a Question&Answer session at the end.
The speakers will be: