Please contact Eilis O’Toole, Clinical Trial Start-up
Study Feasibility Program
We receive feasibility requests through the following:
- HRB CRCI Feasibility service
- From a clinician who has been directly contacted by Pharma
- Directly from a CRO/Pharma company
- From a national or international thematic research network
We have a dedicated feasibility coordinator who navigates local systems and engages with potential investigators, leading to efficient and timely decisions regarding the feasibility of all CRF related studies.
We are part of the HRB CRCI National Study Feasibility Programme which connects academic and industry sponsors with potential investigators. HRB CRCI act as the channel through which study feasibility assessments can be distributed and completed efficiently. We have dedicated personnel here on site to deal with these queries.