ClinDRA™ · Clinical Data Review Assistant
Go from scattered data
to focused clinical review.
Connect study sources, run defined review logic, and investigate the details behind each signal.
- Review study status and areas needing attention.
- Connect adverse events, labs, queries, and subject context.
- Configure checks and outputs for your protocol and team.
Deterministic-first. AI is completely optional.
Inside the product
Start with the study.
Follow the question to the subject.
See the review context.
Select a study scope and population. Review status, safety measures, and operational attention in the same workspace.
Bring a subject’s information together.
- Review subject-level flags and clinical context.
- Move among safety, labs, vitals, queries, and medications.
- Keep reviewer comments connected to the subject.
Follow laboratory results over time.
Explore observed laboratory trajectories for participants with alerts. Review normal and flagged results together, with treatment and study-end context.
Your study determines the configuration
Defined logic.
Useful outputs.
Optional AI.
- Harmonize sources into versioned review data.
- Implement study-specific checks and programs.
- Develop patient profiles, visualizations, and review outputs.
- Define permitted inputs and human review before enabling AI.
Demo screens illustrate selected capabilities. Source coverage, deployment, validation, and review responsibilities are scoped for each implementation.
Start with your study
Show us where review
gets difficult.
Let’s discuss the expertise, review tools, or ongoing support your team needs.