Medical imaging is a cornerstone of the drug and therapy development pipeline, providing safe monitoring and efficacy evaluation. HIRF’s talented team are experienced at conducting phase I, II, and III clinical trials, and are familiar with the rigorous methodology and processes that are required for a successful trial.

HIRF has been involved in clinical trials since 2015, participating in everything from investigator lead to large international multi-centre trials. Most of these trials have been large international multi-centre trials, in a variety of areas such as oncology and progressive neurological disorders.

HIRF can offer support and consultancy from the beginning to the end of your trial.

• Technical support is available for protocol development from our expert team.
• Assistance with the development of trial specific documentation, such as image acquisition manuals.
• Quality assurance using phantoms can be provided to ensure reproducible and quantified measurements, and to ensure harmonisation of multi-site data.
• HIRF has DIAS accreditation.
• Data is anonymised to trial specifics and can be securely transferred to any specified website or node.
• Trial records and data can be stored in secure locations until trial completion.
• Specialist radiology reporting can be organised on request (e.g. LUGANO, RECIST, RANO, DAUVILLE, etc).
• Access to uptake and consultation rooms within HIRF, plus monitoring equipment for patient assessments.
• Blinded or un-blinded reporting of results to CRO as required.
• Support trial vendor audit requirements, including establishment meetings, conference calls, inspections and audits.

For more information on conducting a clinical trial at HIRF, please contact us.