New publications on harmonised standards under the medical devices Regulations
Abstract
Harmonised standards under the Regulations on medical devices and in vitro diagnostic medical devices are developed by CEN and CENELEC as European standardisation organisations, on the basis of a standardisation request issued by the Commission according to Regulation (EU) No 1025/2012. Read the news published by DG Health and Food Safety on 30 January 2026.
Fields of Study & Subjects
Healthcare Regulation
Quality and Safety in Healthcare
Quality and Management Systems
Publication details
- Journal / source
- Hypotheses (OpenEdition)
- Publication date
- 16 February 2026
- Language
- EN