The Department of Health has guidelines for Clinical Trials of Investigational Medicinal Products (CT-IMP)
Health Products Regulatory Authority (HPRA) in Ireland is designated as the Competent Authority for both CT-IMP and Clinical Investigations of a Medical Devices
Recognised RECs under Regulation 7 for Clinical Trials of Medicinal Products.
- Beaumont Hospital Ethics Medical Research Committee
- Clinical Research Ethics Committee of The Cork Teaching Hospitals
- SJH/AMNCH Joint Research Ethics Committee (AKA St. James’/Tallaght University)
- Galway Clinical Research Ethics committee
- HSE North East Area Research Ethics Committee
- HSE South Eastern Area Research Ethics Committee
- Irish College of General Practitioners
- Mater Misericordiae University Hospital/ Mater Private Hospital Institutional Review Board
- National Maternity Hospital Holles Street Research Ethics Committee
- St. Vincent’s Healthcare Group Ethics and Medical Research Committee
- HSE Mid-Western Area and UL Hospital Group Research Ethics Committee