EU HTA Regulation Implementation is an official public source that HealthSignal monitors for Pharmaceuticals, Medical Devices & IVD, Market Access & Reimbursement. The most recent updates we have tracked from it are listed below, each normalised into our index and linked back to the original publication on the source's own website.
Compilation of Joint Clinical Assessment reports, procedural guidance on AI use in HTA dossiers, data transparency principles, and methodological FAQs for medical devices and IVDs.
EU HTA Regulation Implementation · EU-wideGuidance clarifying joint clinical assessment procedures under the EU HTA Regulation.
EU HTA Regulation Implementation · EU-wideFactsheets on joint clinical assessment and scientific consultation procedures under the EU HTA Regulation, plus implementation guidance and analysis of regional cooperation structures.
EU HTA Regulation Implementation · EU-wideGeneral Principles on the use of Artificial Intelligence in the preparation of the JCA dossier Procedural Guidance for Joint Scientific Consultations (JSC) on Medical Devices (MD) and In Vitro Diagnostic Medical Devic...
EU HTA Regulation Implementation · EU-wideTheRegulation (EU) 2021/2282 on health technology assessment(HTAR) entered into force on 11 January 2022 and applies from 12 January 2025.
EU HTA Regulation Implementation · EU-wideNews announcement 8 July 2026 Updated - List of joint clinical assessments 1 min read
EU HTA Regulation Implementation · EU-wideNews announcement 2 September 2025 Updated - List of ongoing joint clinical assessments 1 min read
EU HTA Regulation Implementation · EU-wide