Clinically supervised
Every health-domain decision has medical oversight. Endpoint definitions, adverse events, clinical significance thresholds.
Service · 07 of 07
MD collaboration for clinical study design, health data analysis, epidemiological methods, and CONSORT-compliant reporting. Bespoke scoping required.
What's included
Health & clinical work is scoped individually. Every project includes an MD collaborator from initial design through to reporting. Deliverables are agreed at the proposal stage.
The engagement
Day 0
We discuss your research question, data, and timeline. You'll know by the end of the call whether this service fits — if it doesn't, we'll say so and suggest what does.
Day 1–2
A detailed scope with total cost, timeline, and deliverables. No surprises, no scope creep — you approve before any work begins.
Agreed timeline
Annotated code, documented decisions, and a report structured so that you understand every choice. Two rounds of revisions included as standard.
Why the MD collaboration matters
Every health-domain decision has medical oversight. Endpoint definitions, adverse events, clinical significance thresholds.
CONSORT, STROBE, PRISMA — completed checklists, not a checkbox exercise.
Confounding, selection bias, information bias — identified, measured, and addressed in the analysis.
IRB/ethics applications for health studies require both statistical and clinical input. We provide both.
Pricing
Clinical studies vary too much in scope to quote without a brief. Send a project description and we'll respond with a methodology proposal and a fixed fee.
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