Medical Device Regulation (MDR) and its relation with standardization activities: Presentation in the CEN/TC251 June 2018 meeting in Brussels, Belgium

Alpo Värri

Medical Device Regulation (MDR) and its relation with standardization activities: Presentation in the CEN/TC251 June 2018 meeting in Brussels, Belgium

Research output: Artistic and non-textual form › Digital or Visual Products › Professional

Abstract

The European Union has converted it Medical Device Directive into Medical Device Regulation. This video presents the consequences of the new regulation to the standardization in Health Informatics.

Original language	English
Media of output	Online
Size	338 MBytes
Publication status	Published - 12 Jun 2018
Publication type	I1 Audiovisual publications
Event	CEN/TC251 Plenary meeting: Technical Committee Health Informatics - CEN-CENELEC meeting Centre, Brussels, Belgium Duration: 12 Jun 2018 → 12 Jun 2018

Keywords

medical device regulation
health software
European Union
medical device directive

ASJC Scopus subject areas

Health Information Management
General Computer Science

Access to Document

http://www.cs.tut.fi/~varri/tc251/MDregStd.mp4Licence: CC BY-NC

European Committee for Standardisation (CEN) , Technical Committee 251 (TC251) Health Informatics (External organisation)
Värri, A. (Position of trust)
3 Mar 2016 → 3 Mar 2019
Activity: Membership › Position of trust in public sector

Cite this

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Medical Device Regulation (MDR) and its relation with standardization activities: Presentation in the CEN/TC251 June 2018 meeting in Brussels, Belgium

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Fingerprint

Activities

European Committee for Standardisation (CEN) , Technical Committee 251 (TC251) Health Informatics (External organisation)

Cite this