Health technology assessment - Key documents

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 In-vitro Diagnostic Medical Devices

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

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

PICO exercises

Implementing act on joint scientific consultations on medical devices and in vitro diagnostic medical devices

Implementing Regulation 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)

Procedural Guidance for Joint Scientific Consultations (JSC) on 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)

Guidance on the appointment of assessors and co-assessors for Joint Clinical Assessment (JCA) and Joint Scientific Consultation (JSC)

Procedural guidance for JCA medicinal products

Guidance on the scoping process

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

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)

Implementing Regulation (EU) 2024/2745 on conflict-of-interest rules under the EU Health Technology Assessment Regulation