Gérer la santé publique dans l'UE

Améliorer les systèmes de santé

Promouvoir la santé

Medical devices

Substances of human origin

Sang, tissus et organes

Produits pharmaceutiques

Agir contre les maladies

Évaluation des risques

Comités scientifiques

Endocrine disruptors

Endocrine disruptors

Biocides

Biocides

Dernières mises à jour

11 Janvier 2021

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

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

Updated - Ongoing guidance development within MDCG Subgroups
15 Décembre 2020

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

Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746
20 Octobre 2020

New web page with the basic information on the EUDAMED Actor registration module
06 Octobre 2020

EU device specific vigilance guidance on insulin infusion pumps and integrated meter systems
20 Août 2020

Commission Implementing Regulation (EU) 2020/1207 of 19 August 2020 laying down rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards common specifications for the reprocessing of single-use device

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