The Clinical Research Advisors network model presents some compelling advantages for CROs:

• Our coordinated operations across sites streamline many activities like feasibility assessment, site qualification, training etc. This reduces redundant work.

• For example, a CRO could qualify a main site and its satellites with one visit by leveraging our established SOPs and central oversight.

• Regulatory documents like ICFs, PK consents etc. are pre-approved for our network, minimizing back-and-forth with sites individually.

• Centralized IRB submission through our preferred partners means one product for the CRO rather than multiple submissions.

• Leveraging our eREG, CTMS and eSOURCE platforms allows consolidated source data handling, remote monitoring, and simplified reconciliation.

• Pre-qualified sites, trained staff and tools like AI-screening help accelerate enrollment so CROs can finish studies faster.

• Oversight of all network processes and metrics ensures consistent high quality data CROs can rely upon.

• Our site network has a very divers patient population.

• One contract, one budget, 5 sites, Quick startup, 2 months using central IRB.