Signposting
Primary point of contact for clinical innovation and research, facilitating industry and academia.
Advisory
Consultation on regulatory pathways and provision of advice on conduct of clinical research in all fields.
Study feasibility
Streamlined process with coordination and oversight through the central office and dedicated resource in the CRF/Cs to navigate local systems and engage with Investigators, ultimately leading to efficient and timely identification of sites.
Regulatory, Ethics & Insurance
Management of the application process, including preparation and submission of study documents when feasible.
Study start-up
Range of supports available to optimise start-up activities, including central coordination and dedicated resource in CRF/Cs accelerating all aspects of the process at the site level.
Recruitment
Tracking/monitoring of recruitment targets. Collation of metrics across CRF/Cs and provision of advisory support.
Promotion
Ambassadors for Irish clinical innovation and research, nationally and internationally.
Consultancy
Consultancy support from product concept to commercialisation.
For further information, or to discuss how we can assist you, please contact the HRB NCTO Team.
