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 monitoring services are designed to go hand in hand with our Home Trial Support or Site support services.
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.
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