After completing this course, you will be able to:
- Describe the principles, structure, objectives, and key components of the EU HTA Regulation 2021/2282 (HTAR), and its implications for patients
- Distinguish and outline the HTAR institutional arrangements and processes, including the joint actions, and the roles and responsibilities of Member States
- Discuss patient representation under the HTAR, its purposes, relevance, and how patients can contribute
- Know when and where to access publicly available HTAR information and reports.