EU Health Technology Assessment Regulation (HTAR)

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.