REGULATION (EU) 2017/ 745 OF THE EUROPEAN PARLIAMENT
5 mai 2017 In order for manufacturers to be able to demonstrate the conformity of such products the. Commission should adopt common specifications at ...
Management of Legacy Devices
15 févr. 2021 MDR EUDAMED. 1. EUROPEAN COMMISSION – DG SANTE. 1 INTRODUCTION ... Regulation (EU) 2017/745 (MDR) or Regulation 2017/746 (IVDR).
Implementation Rolling Plan
4 juil. 2022 Article 42(13) MDR. Article 38(13) IVDR. Commission Implementing Regulation (EU) 2017/2185. Definition of the list of codes and ...
COMMISSION IMPLEMENTING REGULATION (EU) 2017/ 2185 - of
24 nov. 2017 Having regard to Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices amending Directive ...
EUROPEAN COMMISSION Brussels 26 May 2021 Until now
26 mai 2021 EUROPEAN COMMISSION. DIRECTORATE-GENERAL FOR HEALTH ... medical devices through a specific chapter of the EU-Switzerland Mutual Recognition.
REGULATION (EU) 2017/ 746 OF THE EUROPEAN PARLIAMENT
5 mai 2017 (21) Directive 98/79/EC allows the Commission to adopt common technical specifications for specific categories of in vitro diagnostic medical ...
Implementation Rolling Plan
20 août 2020 Article 42(13) MDR. Article 38(13) IVDR. Commission Implementing Regulation (EU) 2017/2185. Definition of the list of codes and ...
Guidance for Applicants – Informed Consent
European Commission - Research Directorate-General. Directorate L - Science Economy and Society. Unit L3 - Governance and Ethics. Page 1 of 7.
Unique Device Identification (UDI) System - under the EU medical
Medical Devices (Eudamed) as required by Article 27(3) of MDR and Article 24(3) of IVDR. UDI issuing entities designated by the European Commission.
COMMISSION DELEGATED REGULATION (EU) 2017/ 747 - of 17
17 déc. 2015 THE EUROPEAN COMMISSION. Having regard to the Treaty on the Functioning of the European Union
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