Edinburgh Clinical Trial Pathway

The clinical trial pathway is designed to support investigators through a comprehensive network of specialised stakeholders. Each entity plays a crucial role in ensuring the progression of a trial from conceptualisation to completion.

The Academic and Clinical Central Office for Research and Development (ACCORD) provides research governance and regulatory oversight, ensuring that all trials meet ethical standards and comply with legal requirements, and helping to navigate through the complexities of research governance.

The Edinburgh Clinical Trials Unit (ECTU) offers expertise in trial design, management, and analysis. ECTU works closely with investigators to develop robust study protocols, manage data, and conduct statistical analyses, ensuring scientific rigor and integrity.

Clinical trials requiring dedicated facilities can benefit from the Clinical Research Facility (CRF), which provides state-of-the-art clinical environments, specialised equipment, and trained staff to conduct a variety of clinical studies.

The Edinburgh Research Office (ERO) facilitates funding and grant applications, providing advice on financial aspects, and ensuring compliance with funding bodies’ stipulations.

The CMVM Research Office provides additional support specific to the medical field, including accessing specialist resources..

This integrated support structure ensures that investigators are well-equipped and guided at every step of their clinical trial.