OpenClinica transforms your clinical research through a unified, core electronic data capture (EDC) platform that simplifies the process of running clinical trials in the cloud. With ePRO/eCOA, EHR eSource Integration, Randomization, and Reporting modules, OpenClinica has powered over 10,000 studies worldwide by leading pharmaceutical companies, biotechs, contract research organizations (CROs), academic institutions (AROs), and government agencies.
Why choose OpenClinica?
Support for all types of clinical trials, therapeutic areas and indications
Adaptive platform trials, master protocol trials, umbrella trials, observational research, interventional trials, registries, and real-world evidence research are just a sampling of the types of trials we support. Our experience includes enabling clinical research for some of the first gene therapies to be approved for market and providing better data, faster for COVID-19 research.
Flexible, intuitive electronic case report forms (eCRFs)
Gathering the clinical research data that you need to draw conclusions about a drug, device, or diagnostic should be effortless. OpenClinica’s eCRFs are inherently intuitive. You don’t need to be a programmer to build them and if you need support, our Professional Services team can help you with an array of solutions, including study design and build services fit for your trial.
Better clinical data management
By investing in a partnership with OpenClinica, your clinical data managers can save time, money, and resources (that typically take hundreds of hours and thousands of dollars) to get the clean, accurate data they need. Hear how one clinical data manager used OpenClinica to achieve alone what it often takes whole teams to accomplish.
Serving a wide spectrum of clinical research
OpenClinica is used across a wide spectrum of clinical research, including drug, device, and diagnostic trials. Hundreds of small, midsize, and large research organizations leverage OpenClinica to capture better clinical data faster.
Compliance and quality
go hand-in-hand
We apply strict adherence to regulatory requirements in everything we do, following all applicable guidelines and regulations. Not only do we prioritize compliance and quality, but we enable our clients to be compliant in the areas they need to be as well. We follow: 21 CFR Part 11, Annex 11, GDPR, and HIPAA regulations.
Over 10,000 studies and counting…
We have supported clinical trials on six of the seven continents spanning Phase I-Phase IV research as well as academic studies.
Resources
Check out our free tools and thought leadership to learn more about clinical data management, electronic data capture, ePRO/eCOA, decentralized clinical research, and more!