The EU HTA Regulation: Webinar for health technology developers of medical devices and in vitro diagnostic medical devices
Abstract
This webinar explained the process for joint clinical assessments and joint scientific consultations for high-risk medical devices and in vitro diagnostic medical devices, and the European Commission demonstrated the HTA IT Platform which is used for secure exchange of information with health technology developers. Read the news published by EC Directorate-General for Health and Food Safety on 23 December 2025.
Fields of Study & Subjects
Healthcare Regulation
Health Systems
Economic Evaluations
Quality of Life
Biomedical Ethics and Regulation
Publication details
- Journal / source
- Hypotheses (OpenEdition)
- Publication date
- 11 February 2026
- Language
- EN