EU action on health

Improving health systems

Promoting good health

Medical devices

Substances of human origin

Blood, tissues, cells and organs

Pharmaceuticals

Diseases and health threats

Risk assessment

Scientific committees

Endocrine disruptors

Endocrine disruptors

Biocides

Biocides

Latest updates

13 April 2021

Registration open: Webinar for Patients – Safe and performant Medical Devices for all (26 May 2021)
09 April 2021

Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746
09 April 2021

Updated Implementation Rolling Plan - Regulation (EU) 2017/745 and Regulation (EU) 2017/746
01 April 2021

The expert panels in the field of medical devices now accept submissions from notified bodies for the Clinical Evaluation Consultation Procedure
23 March 2021

Infographic - Is your software a Medical Device?
15 March 2021

Guidance on state of the art of COVID-19 rapid antibody tests
15 March 2021

Questions and Answers on Custom-Made Devices
26 February 2021

Guidance on harmonised administrative practices and alternative technical solutions until EUDAMED is fully functional
24 February 2021

COVID-19 tests: Q&A on in vitro diagnostic medical device conformity assessment and performance in the context of COVID-19
18 January 2021

Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities

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