Health technology assessment - Key documents

Report on Emerging Health Technologies

2026 Work Programme - Member State Coordination Group on HTA (HTACG)

Guidance on the HTACG recommendation for the selection of medical devices and in vitro diagnostic medical devices for JCA

Procedural Guidance for JCA medical devices and in vitro diagnostic medical devices

Questions and Answers on general methodological and procedural issues for joint clinical assessments

Guidance on filling in the joint clinical assessment (JCA) dossier template – Medical devices and in vitro diagnostic medical devices

Implementing Regulation (EU) 2025/2086 on joint clinical assessment of medical devices and in-vitro diagnostic medical devices

Briefing document template for parallel HTACG/Expert Panels JSC for medical devices

Guidance for the selection of Medical Devices (MD) and In Vitro Diagnostic Medical Devices (IVD) for Joint Scientific Consultations (JSC)

Procedural Guidance for Joint Scientific Consultations (JSC) on Medical Devices (MD) and In Vitro Diagnostic Medical Devices (IVD)

Briefing document template for HTA-only Joint Scientific Consultation of Medical Devices

Briefing document template for HTA-only Joint Scientific Consultation of In-vitro Diagnostic Medical Devices

Outcome document template for the Joint Scientific Consultation of Medical Devices and In-vitro Diagnostic Medical Devices

PICO exercises

Implementing Regulation (EU) 2025/117 on joint scientific consultations on medical devices and in vitro diagnostic medical devices

Implementing Regulation (EU) 2024/3169 on the procedures for joint scientific consultations on medicinal products for human use at Union level

2025 Work Programme - Member State Coordination Group on HTA (HTACG)

Guidance on filling in the joint clinical assessment (JCA) dossier template – Medicinal products

Procedural guidance for JCA medicinal products