For clinical research
Prescreen participants with their real history.
Flexpa can supply participant-authorized claims and clinical records for clinical trial prescreening. Researchers can review available diagnoses, procedures, medications, and lab results against inclusion and exclusion criteria. Records vary by source and do not replace the study team's eligibility assessment or required tests.
Updated 2026-11-11
How it works
- Participant authorizes supported sources
- Retrieve available records
- Researchers review study criteria
What to review
- Recorded diagnoses and procedures relevant to the protocol.
- Medication information present in the connected sources.
- Available lab results, with their dates and units.
Keep unresolved criteria visible
Use the retrieved records as an input to prescreening. Do not interpret an absent result as a negative finding or assume that a historical result establishes a participant's current status.
Questions
How can claims data support clinical trial prescreening?
Flexpa can retrieve participant-authorized records for researchers to review against study criteria. Available claims can show recorded diagnoses and procedures; connected clinical sources may add lab results and other details. The study team still determines eligibility.
Does Flexpa replace screening visits or lab tests?
Flexpa retrieves available health records for prescreening. Do not use those records as a substitute for visits or tests required by the study protocol, or assume every required result will be available.