We are the world’s first digital contract research organization (CRO). We contract with biotechnology and pharmaceutical firms to run pragmatic clinical trials for peer-reviewed publication and regulatory purposes.

Our team includes industry leaders in secure transfer and use of complete EHR data, clinical natural language processing, healthcare artificial intelligence, and healthcare data policy. We have run studies and defined cohorts for the leading academic medical centers, the National Institutes of Health, and the National Science Foundation. We have testified before Congress in the 21st Century Cures Initiative and helped shape policy in use of advanced clinical data and technologies.

We welcome the opportunity to show you the state of the art, let you work with data in an easy to use graphical interface, and expand the future of medical knowledge together.

 

Comparison of a traditional versus digital CRO

Trial Step Traditional CRO RWE CRO
Protocol definition Focused on human subjects protection Focused on data security and analytic methodology
Academic medical center engagement Clinical division relationships Bioinformatics division relationships
IRB approval Clinical practices Security and privacy
Patient recruitment Workflow related Natural language processing and cohort definition
Trial arm distribution Clinical intervention Artificial intelligence
Validate information Clinical monitoring Drill down capabilities and manual annotation