How We Help Sponsors
Identification
Use evidence-based data to target sites with the right patients for your trial
Feasibility Questionnaire
Access responses in real-time for quick insight on your site’s capability to conduct the trial
Site Visit
Schedule dates for Pre-Study Site Visit and Site Initiation Visit to qualify sites, and provide training
Clinical Trial Agreement
Expedite contracts and initiate sites to accelerate patient enrollment
Regulatory / IRB
View regulatory essential documents and manage IRB/Ethics approvals
Drug Shipment
Monitor drug request and shipment
Enrollment
Track screening and enrollment to confirm activation
How We Help Sites
CDA
Expedite the Confidential Disclosure Agreement with auto-fills and digital signature
Feasibility Questionnaire
Immediate access to questionnaires to provide insights on site capability
Qualification
Provide required documents and coordinate sponsor visits
Clinical Trial Agreement
Facilitate negotiations on contracts with accuracy and clear communication
Regulatory / IRB
Upload essential regulatory documents and track IRB/Ethics submission and approvals
Enrollment
Report and track screening and enrollment to confirm activation
What Do Customers Think…
Clients
We are proud to be recognized by MD Tech Review for our advancements in the clinical space!
To learn more about our first-of-its-kind Study Start-Up System (SSUS) and read the Q&A with our Founder and President, please click here.