Feasibility and site selection
We have a network consisting of a significant number of high quality clinical sites and many cross-links to other established clinical trial networks. We can run feasibility and site selection processes on a global level or on a country specific level.
ITREAS operates a feasibility system that allows for investigator friendly distribution of feasibility documentation, as well as the subsequent analysis and follow-up. Our system is built to incorporate the study specific selection criteria and generates reports and metrics on a site level as well on an aggregate level in order to closely track progress of the feasibility and selection process. In addition, we can also track the start-up and site initiation process.
Regulatory and ethics committee submissions
ITREAS can assist you to speed up your regulatory and ethics committee submissions to ensure that there is a minimum gap between site selection and site initiation and timelines are kept. We can assist with the review of essential documents such as ICFs (Informed Consent Forms) and we can help with the contract and budget negotiations. We can perform these services as stand-alone deliverable or we can set-up a formal body of national coordinators to perform these services.