Automated, reusable workflows, intuitive interfaces and clear dashboards simplify and improve experience and outcomes. We deliver a flexible platform of best-in-class solutions that work beautifully together or as standalone solutions: EHR-to-EDC Integration | eSource | EDC | ePRO & eCOA | eConsent | Patient-Level Data Capture | Randomization & Supply Chain | Data Analytics
From recruitment to study lock, we've got you.
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EHR to EDC eSource
Auto-populate EDC & eCRFs with regulatory-grade source data from patient EHRs in real-time. Unite is a device-agnostic solution that’s proven & scalable. Loved by research staff. Valued by sponsors. Learn more
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Electronic Data Capture
Speed up study start with our EDC’s intuitive form builder. Maintain momentum with automated workflows & notifications, smart eCRFs, and protocol automation for participant and research scheduling. Learn more.
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ePRO & eCOA
Keep participants engaged, ease clinician burden and get higher-quality results earlier with anytime, anywhere, any device outcome reporting. Learn more.
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eConsent
Deliver an engaging consent experience to boost recruitment, retention and onboarding with total electronic consent management. Learn more.
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Randomization & Supply Chain
Create easy, automated workflows for total randomization and supply chain management right within eCRFs. Learn more.
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Data Analytics
Visualize, analyze and share key trial analytics in real-time with out-of-the-box library of reports and dashboards. Easily build and share customized insights to meet your unique trial needs. Learn more.
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15,000+Clinical trials across 100+ countries
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3 Million+Participants supported
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500+Customers trust OpenClinica
The best way to learn about us is to have a conversation.
The OpenClinica Difference
Support for all types & phases of clinical trials
Adaptive platform, master protocol, device, umbrella, observational, interventional, digital therapeutics (DTx), plus registries and real-world evidence research are just a sampling of the types of trials we support. Our flexible framework delivers unparalleled support for trials in all types & phases of clinical research.
Serving all indications & therapeutic areas
Our flexible, scalable, intelligent, no-code/low-code solutions are ideal for all indications and therapeutic areas. Our customers include large-scale, multi-year adaptive platform oncology trials, extensive diabetes trials, cell and gene therapy research, biotechnology studies, cardiovascular disease research, rare disease and orphan drug development, infectious disease trials, neurology studies, mental health and psychiatry research, immunology and inflammatory disease trials, pediatrics, dermatology studies, ophthalmology research, respiratory disease trials, and regenerative medicine.
Loved by researchers
Our solutions are developed & constantly refined with the busy researcher front-of-mind. Always. We believe that gathering & analyzing study data should be effortless and that turning protocols and protocol changes into eCRFs should be a breeze. We believe technology should enable site & study teams to focus on high-value scientific research and patient-focused care.
Valued by leadership
By automating and simplifying data management & analysis, site leadership can take on more studies; sponsors can get early, reliable data for better decision making, academic research organizations can do better research, CROs can gain a competitive advantage, and most importantly, people can get the therapies they need sooner.