Authors
Directorate-General for Health and Food Safety, European Commission
- CELEX
- 32024R1381
- Catalogue number
- FXL2401381EN
- Citation
- Commission Implementing Regulation (EU) 2024/1381 of 23 May 2024 laying down, pursuant to Regulation (EU) 2021/2282 on health technology assessment, procedural rules for the interaction during, exchange of information on, and participation in, the preparation and update of joint clinical assessments of medicinal products for human use at Union level, as well as templates for those joint clinical assessments (OJ L, 2024/1381, 24.05.2024, ELI: http://data.europa.eu/eli/reg_impl/2024/1381/oj )
- ELI
- reg_impl/2024/1381/oj
- IMMC
- C(2024)3320/3327829
- ISSN
- 1977-0677
- OJ
- L_202401381
- Pages
- 00033
- Published in
- Belgium
- Size
- 3.3x297.0x210.0MM
- weight
- 82.0
Table of Contents
- Commission Implementing Regulation (EU) 2024/1381 of 23 May 2024 laying down, pursuant to Regulation (EU) 2021/2282 on health technology assessment, procedural rules for the interaction during, exchange of information on, and participation in, the preparation and update of joint clinical assessments of medicinal products for human use at Union level, as well as templates for those joint clinical assessments 1
- ANNEX I 16
- Appendixes 26
- ANNEX II 28
- Appendixes 32
- ANNEX III 33