We will collect and verify your essential documents.
We will coordinate your third party vendors/suppliers.
We will organise the trial master file and compilation of investigator site files, and site/study reference manual.
We will manage the investigator contracting process, ethics committee submissions and R&D approvals.
Finally, we will ensure the site is ready to recruit, including Study Site Coordinator training (if required).
Telephone enquiries: +44 (0) 1837 82165
Site Selection & Qualification
Clinical Operations Advice