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Accelerating Clinical Trials in the EU
Support mechanisms for non-commercial clinical trials Level
NationalEU Level (Multinational)Global
Dedicated webpage    
Training courses    
Scientific advice The National Competent Authority (NCA), HPRA, supports scientific advice with no fee/reduced fee.  X 
Helpdesk, regulatory, CTIS and ethics supportRegulatory and ethics requirement: Available from the NCA (HPRA) and ethics committees (NO-NREC). X 
Other services by National Competent Authority 

NCA: Effective as of 1 January 2024, non-commercial sponsors are no longer required to pay Clinical Trial Application fees in Ireland. For more information: HPRA fee guide.

Inspection fee: The HPRA supports inspection fee reduction/waiver. For more information: HPRA fee guide.

Scientific support: For example: HRB TMRN (HRB Trials Methodology Research Network).

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Services by ethics committee

Effective as of 1 January 2024, non-commercial sponsors are no longer required to pay Clinical Trial Application fees in Ireland.

For more information: Fees - NREC (nrecoffice.ie)

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Public GCP support    
Public research officeFor example: HRB NCTO (HRB National Clinical Trials Office)X  
National funding and other financial support

The HRB (Health Research Board) operates a funding scheme called Definitive Intervention and Feasibility Awards (DIFA). DIFA supports researchers and research teams to conduct high-quality definitive intervention trials and feasibility studies.

For more information: Funding schemes (hrb.ie)

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Funding coordination and navigation of research infrastructure    
Support identifying research networksFor example: HRB NCTO (HRB National Clinical Trials Office)X  
Other support mechanisms

The HRB NCTO is an independent, integrated, national clinical research network, which provides centralised support in conducting multi-centre clinical trials and investigations across Ireland.

For academic studies, NCTO offers guidance on all aspects of delivering the study within Ireland, such as on regulatory pathways, site identification and feasibility assessments, and introduces the academic PI to the local experts at seven clinical research facilities/centres in Ireland. The local CRF/C can provide the services necessary to carry out a clinical study/trial, including clinical research nursing, data management, statistics etc. 

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