Latest news
MedTech Europe publishes a Call to Action on the MDR to keep devices available to patients
Posted on 06.02.2020
Read moreSwiss Regulation on integrity and transparency in the field of medicinal products entered into effect on 1 January
Posted on 06.02.2020
Read moreMedTech Europe’s participation in the public consultation on Article 25 Data Protection by Design and by Default Guidelines of the EDPB
Posted on 06.02.2020
Read moreEuropean Data Protection Supervisor (EDPS) publishes Preliminary Opinion on data protection and scientific research
Posted on 06.02.2020
Read moreThe MedTech Forum 2020 – Last chance to register with the Early Bird rate
Posted on 06.02.2020
Read moreAn interoperability training with IHE Europe on 27 March 2020 in Brussels
Posted on 06.02.2020
Read moreShining a light on medtech – Raising awareness on the role of medtech in everyone’s life
Posted on 05.02.2020
MedTech Europe launches a communications campaign to raise awareness on the role of medical technologies, from diagnosis to cure.
Read moreMedical Devices Regulation: EU takes action to facilitate continued availability of certain low-risk medical devices to patients and healthcare systems
Posted on 18.12.2019
Brussels, 18 December 2019 – With the approval by the European Parliament yesterday, the European Union (EU) has brought additional clarity regarding the transitional provisions of the Medical Devices Regulation (MDR).