Simple EDC
Trial setup that takes just two weeks from protocol finalization
Study startup is a major bottleneck in clinical trials. Sites are ready to recruit, but your data collection instrument isn't. The traditional model—contracting a vendor and manually programming forms—is an outdated, slow way of working.
We do things differently. Starting directly with your trial protocol and documentation, we automatically extract your core requirements to generate a fully programmed CRF—complete with audit trails and data validation checks. We can get your study up and running within two weeks of receiving your protocol.
