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New medtech regulations

Second Corrigenda to the MDR and IVDR

Posted on 06.02.2020

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New medtech regulations

MedTech Europe publishes a Call to Action on the MDR to keep devices available to patients

Posted on 06.02.2020

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MedTech Europe

MedTech Week 2020 – Save the date

Posted on 06.02.2020

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MedTech Europe

MedTech ON AIR: the first episode is online!

Posted on 06.02.2020

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Interactions with the Medical Community

Swiss Regulation on integrity and transparency in the field of medicinal products entered into effect on 1 January

Posted on 06.02.2020

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Newsletter

MedTech 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

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Interactions with the Medical Community

European Data Protection Supervisor (EDPS) publishes Preliminary Opinion on data protection and scientific research

Posted on 06.02.2020

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Newsletter

SNITEM Start-up day

Posted on 06.02.2020

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MedTech Europe

The MedTech Forum 2020 – Last chance to register with the Early Bird rate

Posted on 06.02.2020

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Digital Health

An interoperability training with IHE Europe on 27 March 2020 in Brussels

Posted on 06.02.2020

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Shining a Light

Shining 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.

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Medical 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).

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