Project Lead: Ingrid Zechmeister-Koss
Project Team: Ingrid Zechmeister-Koss, Sabine Ettinger, Gregor Goetz, Judit Erdös
Duration: ongoing
Language: German
In January 2025, the EU HTA Regulation came into force. The AIHTA plays a central role in the implementation of the Regulation – covering both medicines and medical devices – in terms of technical collaboration, national coordination and international representation.
This primarily involves the following tasks:
- Committee work: Participation in the HTA Coordination Group, JCA, EHT and Methods subgroups; ongoing coordination with national institutions.
Training & evaluation: Participation in the EU HTA training programme; preparation of the Member State report (deadline: 01/2027) for the evaluation of the EU HTA Regulation (by 01/2028).