Webinar WG 2: Medical Device Regulations – Software as Medical Device

The event is provided by the COST Action 19132 ENABLE, Working Group 2. 

CA19132–ENABLE: “European Network to Advance Best practices & technology on medication adherencE” is a COST Action supported by Horizon 2020 Framework Program funded by European Union.

When: 14th October 2021 at 4pm (CEST)



45 minutes: Presentation of the new European Regulation for medical devices (MDR)

15 minutes: Discussion 


  • Mariana MADUREIRA, Medical Devices Competent Authority – INFARMED, Portugal

Mariana Madureira is responsible for coordinating activities related to projects, within the scope of implementation of new medical devices regulations at Health Products Directorate at the National Authority of Medicines and Health Products (INFARMED), in Portugal. She has also a role of assessor of medical devices on the pre-market and market surveillance activities….