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Elamine, töötamine ja reisimine ELis
Rahvatervis
Medical Devices - EUDAMED
Medical Devices - EUDAMED
Kõik teemad
Overview
Actors registration
ELi rahvatervise juhtimine
Tervisestrateegia
State of Health in the EU
Tervishoid ja struktuurifondid
EL maailmas
Tervisenäitajad
Improving health systems
Piiriülene tervishoid
European Reference Networks
E-tervis
Tervishoiutehnoloogia hindamine
Tervishoiutöötajad
Health systems performance assessment
Expert Panel on effective ways of investing in health
Hea tervise edendamine
Tubakas
Toitumine ja kehaline aktiivsus
Alkohol
Sotsiaalsed tegurid ja tervishoiualane ebavõrdsus
Medical devices
Medical Devices - Sector
Medical Devices - New regulations
Medical Devices - Topics of Interest
Medical Devices - Dialogue between interested parties
Medical Devices - Expert Panels
Medical Devices - EUDAMED
Substances of human origin
Veri, koed ja elundid
Farmaatsiatooted
Inimtervishoius kasutatavad ravimid
EudraLex
Union Register
Pharmaceutical committee and expert groups
European Medicines Agency (EMA)
Haigustevastased meetmed
Health security and infectious diseases
European Centre for Disease Prevention and Control (ECDC)
Vaktsineerimine
Antimikroobne resistentsus
Rasked ja kroonilised haigused
Cancer
Mental health
Riskihindamine
Teaduskomiteed
Endocrine disruptors
Endocrine disruptors
Biocides
Biocides
Viimased uuendused
03 September 2021
The expert panel in the field of in vitro diagnostic medical devices now accepts submissions from notified bodies for the Performance Evaluation Consultation Procedure
15 Juuni 2021
European Medical Device Nomenclature (EMDN) - Questions and Answers
18 Mai 2021
The UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI system.
01 Detsember 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
20 Oktoober 2020
New web page with the basic information on the EUDAMED Actor registration module
15 Juuli 2020
Factsheet on MDR requirements for Transparency and Public Information
E-uudiskiri
E-uudiskiri
E-uudiskiri
Mon, 05/31/2021
Enneta. Kaitse. Immuniseeri: Euroopa immuniseerimise nädal 2021
Viimased uuendused
The expert panel in the field of in vitro diagnostic medical devices now accepts submissions from notified bodies for the Performance Evaluation Consultation Procedure
Avaldamise kuupäev
03 September 2021
Jälgige meid Twitteris
Veel
Aktuaalne
The UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI system.
Factsheet on MDR requirements for Transparency and Public Information
Seonduv teave
Väljaanded
