Leveraging our deep domain expertise we found the crucial, objective data required for every clinical trial and then built an algorithm to access, extract, normalize, index and integrate the data to create a customizable site identification platform. AcceleTrial combines site identification, feasibility, and activation in a singular unique process to speed up the startup of clinical trials.
The only way to have a meaningful and measurable impact on site startup is through more accurate, objective, evidence based site identification.
Use evidence-based data to target sites with the right patients for your trial
Access responses in real-time for quick insight on your site’s capability to conduct the trial
Schedule dates for Pre-Study Site Visit and Site Initiation Visit to qualify sites, and provide training
Expedite contracts and initiate sites to accelerate patient enrollment
View regulatory essential documents and manage IRB/Ethics approvals
Monitor drug request and shipment
Track screening and enrollment to confirm activation
Expedite the Confidential Disclosure Agreement with auto-fills and digital signature
Immediate access to questionnaires to provide insights on site capability
Provide required documents and coordinate sponsor visits
Facilitate negotiations on contracts with accuracy and clear communication
Upload essential regulatory documents and track IRB/Ethics submission and approvals
Report and track screening and enrollment to confirm activation