The EU Medical Device Regulation (Regulation 2017/745) (EU MDR) and In Vitro Diagnostics Regulation (Regulation 2017/746) (EU IVDR) require the sponsors of clinical investigations and certain performance studies to be established in the EU (or Northern Ireland) or have a legal representative established in the EU (or Northern Ireland).
You are invited to participate in this survey of the training needs of people interested in training from Evidence Synthesis Ireland.
The survey is for stakeholders including researchers, healthcare professionals, policy-makers, students, academics, information specialists, patients and the public, and other generators and users of evidence syntheses.
Please note our workshops are primarily for those resident on the island of Ireland.
From autumn 2023, the number of funding opportunities created by the HSC R&D Division investment in National Institute for Health and Care Research (NIHR) funding programmes is increasing. The Evidence Synthesis programme, Invention for Innovation (i4i), Research for Social Care (RfSC), Programme Grants for Applied Research programme (PGfAR) and Programme Development Grants have been added to the suite of programmes accessible to NI Chief Investigators
