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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

Research output: Artistic and non-textual formDigital or Visual ProductsProfessional

Details

Original languageEnglish
Media of outputOnline
Size338 MBytes
Publication statusPublished - 12 Jun 2018
Publication typeI1 Audiovisual material
EventCEN/TC251 Plenary meeting: Technical Committee Health Informatics - CEN-CENELEC meeting Centre, Brussels, Belgium
Duration: 12 Jun 201812 Jun 2018

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.

Keywords

  • medical device regulation, health software, European Union, medical device directive

Publication forum classification

Field of science, Statistics Finland