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Newsletter
Call for expression of interest for expert panels on medical devices and in vitro diagnostic medical devices
Posted on 03.10.2019
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New medtech regulations
Revised Manufacturer Incident Reporting form and new Vigilance-related guidance documents published
Posted on 03.10.2019
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New medtech regulations
Summary of Safety and Clinical Performance guidance published to support the implementation of the MDR
Posted on 03.10.2019
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Digital Health
MedTech Europe published digital health interoperability position paper
Posted on 03.10.2019
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MedTech Europe
European Patients’ Forum (EPF) and MedTech Europe hold Patient-Medtech Dialogue workshop
Posted on 04.07.2019
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European Union
Implementation tools to help transitioning from Directives to Regulations
Posted on 04.07.2019
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New medtech regulations
Industry Perspective on the Implementation Status of the MDR/IVDR
Posted on 04.07.2019
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New medtech regulations
European database on medical devices (EUDAMED)
Posted on 06.06.2019
The European Commission has recently set up a new webpage to collect information that is related to the implementation of the upcoming European database on medical devices (EUDAMED). The website is expected to be updated regularly upon new implementation documents are finalised.
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