Services > Trial Management Support

The MRN is able to run and manage all aspects of clinical trials, from specialised feasibility via site placed nurses through to database lock and reporting. Services include:

Site selection, ethics & initiation
• All aspects of site set up, from initial feasibility through to site initiation.
• All critical documentation can also be collated, as well as ethics approvals sought on a per site basis and drug release approved in line with ICH GCP requirements.

Monitoring activities
• Our unique approach to monitoring utilises 100% electronic data collection, even in the patient’s homes, reducing the requirement for source data verification whilst increasing the quality of the data collected.

Project management
• Overall trial management from kick off through to final deliverable, utilising detailed study plans and SOPs to ensure all trials are delivered on time and within budget.

Data management
• All aspects from CRF design through to database lock and reporting.
• Fully integrated electronic data acquisition solutions from both the patients’ home and the research site.

EDC solutions are provided by our partner, Datatrak International.