Health technology assessment - Key documents

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

Guidance on the scoping process

Procedural Guidance for Joint Scientific Consultations (JSC) on Medicinal Products (MP)

Briefing document template for Joint Scientific Consultation (JSC) for Medicinal Products (MP)

Briefing document template for Parallel HTA Coordination Group (HTACG)/European Medicines Agency (EMA) Joint Scientific Consultation (JSC) for Medicinal Products (MP)

Guidance for the selection of Medicinal Products (MP) for Joint Scientific Consultations (JSC)

Outcome document for Joint Scientific Consultations (JSC) on Medicinal Products (MP)