Trusted Partnerships
Trusted by thousands of researchers across public and private sectors.











Built for the people who run clinical research
Clinical research runs on
incomplete records. We fix that.
Six things our clients have that they did not have before.
01
Enroll faster. Complete histories arrive before the screening visit, so eligibility is decided once. Records in under 24 hours instead of four to six weeks.
02
Fewer screen failures. Missing labs and prior treatments stop being discovered on screening day. Sites screen the right patients the first time.
03
Less site burden. No chasing faxes, no manual chart abstraction, no re-keying. Coordinators run the study instead of the paperwork.
04
Reach patients you can actually enroll. Consent makes each candidate contactable, so feasibility becomes enrollment on one platform instead of a handoff to another vendor.
05
Keep patients after enrollment. Continuous longitudinal records without extra visits. Retention, outcomes, and safety signals stay visible for years.
06
Evidence that holds up. FDA 21 CFR Part 11 chain of custody from consent to export. Data that stands in a submission, not just a slide.



