Page: Class III implantable devices and Class IIb medical devices intended to administer or remove medicinal products: expert panel opinions-2026/3/10

Page: High-risk medical devices: consultation procedures-2026/3/10

Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2026/3/10

Document: European Medicines Agency’s data protection notice for the EudraVigilance Signal and Safety Analytics (EV SSA) platform-2026/3/10

Page: Supporting innovation-2026/3/10

Page: Portfolio and technology meetings-2026/3/10

Document: Portfolio and technology meeting briefing document-2026/3/10

Document: Procedural guidance to scientific committeesꞌ members and experts on completing the European Medicines Agencyꞌs declaration of interests in the Experts Management Tool-2026/3/10

Document: Methodology to identify vulnerabilities in supply chains of critical medicines-2026/3/10

Document: SMS guidance for external users-2026/3/10