Research intelligence
Research Agent
Synthesize research context, evidence gaps, and cohort questions for human research teams.
Human review
before study design, patient outreach, publication, or operational decision
research lead, IRB owner, or qualified clinician reviewer
01no IRB bypass
02no unsupported clinical claim
03human research approval required
Minimum context required before workflow execution.
- research question
- cohort criteria
- literature summary
- data availability
Reviewable artifacts the agent can produce.
- research brief
- cohort feasibility questions
- evidence gap summary
Connector targets this workflow may eventually depend on.
- research platforms
- data warehouses
- clinical registries
Least-privilege capabilities allowed for this workflow.
- read research fixtures
- summarize evidence
- draft research operations brief
Events that must remain observable and reviewable.
- brief drafted
- evidence gap logged
- cohort question created
- review disposition recorded
No SCRIMED agent should operate beyond explicit scope, consent, permissions, and review policy.
Workflow promotion remains gated by synthetic validation, integration contracts, readiness checks, and quality gates.