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Elamine, töötamine ja reisimine ELis
Rahvatervis
Medical Devices - Topics of Interest
Medical Devices - Topics of Interest
Kõik teemad
Ülevaade
Teavitatud asutused
Seadme kordumatu identifitseerimistunnus (UDI)
Taastöötlemine
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
Riskihindamine
Teaduskomiteed
Endocrine disruptors
Endocrine disruptors
Biocides
Biocides
Viimased uuendused
23 Märts 2021
Infographic - Is your software a Medical Device?
08 Märts 2021
Updated version - Information on the applications for designation as a notified body (short overview)
18 Jaanuar 2021
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
11 Jaanuar 2021
Covid-19: Commission Notice on audits to be performed by notified bodies
11 Detsember 2020
Updated presentation - Information on the applications for designation as a notified body under Regulations (EU) 2017/745 and 2017/746
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
13 Juuli 2020
Survey on availability and capacity of notified bodies to carry out conformity assessments for COVID-19 essential devices
12 Juuli 2020
Amendment to Implementing Regulation 920/2013 on the designation of notified bodies
12 Juuli 2020
MDCG 2020-11: Guidance on the renewal of designation and monitoring of notified bodies
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Viimased uuendused
Infographic - Is your software a Medical Device?
Avaldamise kuupäev
23 Märts 2021
Updated version - Information on the applications for designation as a notified body (short overview)
Avaldamise kuupäev
08 Märts 2021
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Aktuaalne
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
Commission Notice on notified bodies’ audits performed during Covid-19 exceptional circumstances
Commission guidelines on Union-wide derogations for medical devices
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