Vendor sprawl and start-up delays kill momentum. OpenClinica gives sponsors total visibility, fast launches, and clean data from day one.
Sponsors running global, multi-site trials
Biotech, pharma, and medical device companies running clinical trials, patient registries, and long-term evidence programs
Teams seeking fewer vendors and faster study launches
One system for data, consent, and oversight
Dashboards from executive to site level
Rapid site onboarding and IRB-ready templates
Built-in EDC, randomization, eCOA, and coding
Transparent pricing aligned with study volume
Connect Recruit to EDC for full pipeline visibility
Scope global needs, then configure studies in one environment
Onboard sites with training, templates, and permissions
Real-time data, consent, and randomization flow into dashboards
Use full audit trails for regulatory submission
Tell us about your needs. Our team will help you find the right solution and answer any questions about how OpenClinica can support your work.
