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