Dirigir la salud pública de la UE

Improving health systems

Promover la salud

Medical devices

Substances of human origin

Sangre, tejidos y órganos

Medicamentos

Combatir las enfermedades

Evaluación de riesgos

Comités científicos

Endocrine disruptors

Endocrine disruptors

Biocides

Biocides

Actualizaciones más recientes

26 Febrero 2021

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

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

Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
11 Enero 2021

Covid-19: Commission Notice on audits to be performed by notified bodies
18 Diciembre 2020

Updated Implementation Rolling Plan - Regulation (EU) 2017/745 and Regulation (EU) 2017/746
18 Diciembre 2020

Updated - Ongoing guidance development within MDCG Subgroups
15 Diciembre 2020

MDCG 2020-18 - MDCG Position Paper on UDI assignment for Spectacle lenses & Ready readers
02 Diciembre 2020

MDCG 2020-17 - Questions and Answers related to MDCG 2020-4: “Guidance on temporary extraordinary measures related to medical device notified body audits during COVID-19 quarantine orders and travel restrictions”
01 Diciembre 2020

The EUDAMED Actor module is in production. On 1st December 2020 the European Commission has made available the Actor registration module to Member States and economic operators
13 Noviembre 2020

Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746

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