Cited feasibility for CROs & sponsors
Cited feasibility your CRO can bid with — and defend.
Protocol in, cited go/no-go verdict out — in hours. Every number traces to its public source, on a Part 11 audit trail. White-label and ready for your bid.
Site density and cohort reach, scored across every trial region.
Built on public data sources
Public, re-verifiable sources — click any number to check it yourself. Your protocol is never used to train a model.
The moat
The opposite of a black box.
One verdict, read two ways: defensible enough for your board, transparent enough for your engineers.
For the buyer
- Defensible to your board and the FDA
- Hours, not a six-week cycle
- Built on public data anyone can re-verify
- No proprietary lock-in
For the builder
- Every number resolves to a public-source URL
- Deterministic scorers, not model guesses
- Part 11 tamper-evident hash chain
- Self-hosted Qwen — no third-party model sees your protocol
The problem
A multi-million-dollar go/no-go shouldn't rest on a report you can't audit.
If you run a CRO bid team, you know the math: a $100k, six-week feasibility cycle is fine when you win the bid and unsustainable when you lose it — and a sponsor can still pick the number apart. The same is true for a biotech or academic IST unit making an irreversible bet. Today that evidence arrives slow, opaque, and impossible to check.
Speed
A six-week CRO feasibility questionnaire is too slow for a go/no-go decision that keeps moving. By the time the report lands, the window has narrowed.
Defensibility
When your board — or the FDA — asks where a number came from, "the model said so" is not an answer. You need a verdict anyone can trace back to a public source.
Cost
Bespoke feasibility consulting costs five or six figures per protocol — before you have even decided whether the trial is worth running.
How it works
Protocol in. Cited verdict out. In hours.
Ingest
Upload your protocol PDF. A self-hosted LLM extracts the endpoints, eligibility criteria, and trial design — your document never leaves our infrastructure for a third-party model.
Pull public data + score
We query ClinicalTrials.gov, PubMed, FDA, EMA, Open Targets, AACT, and ChEMBL, then run deterministic scorers for PTRS, budget, site density, and cohort reachability.
Cited verdict
You get a verdict where every number carries its source plus a tamper-evident Part 11 hash. Export the whole thing for your board or the FDA.
How it compares
Faster than a CRO. Defensible unlike a chatbot.
A feasibility verdict that's quick to get and impossible to wave away.
| Capability | CRO questionnaire | Black-box AI | Feasibility Studio |
|---|---|---|---|
| Turnaround | 4–6 weeks | Minutes | Hours |
| Every number traced to a public source | |||
| Deterministic scorers (re-runnable) | |||
| 21 CFR Part 11 tamper-evident audit chain | |||
| Your protocol never trains a model | |||
| Cost per protocol | 5–6 figures | Low | Flat per-run |
For developers
A feasibility verdict from one API call.
POST a protocol, get back a cited, scored, Part-11-audited verdict.
- One POST, a fully cited, scored verdict back.
- Token auth + per-tenant isolation — your data never trains a model.
- Part 11 audit hash on every response.
curl https://api.feasibility.studio/v1/feasibility \ -H "Authorization: Bearer $TOKEN" \ -F protocol=@protocol.pdf # response — every figure carries its source # verdict: CONDITIONAL GO # ptrs: 58% (source: opentargets) # eligible_us: 24,300 (source: aact) # audit_hash: e7a1…9f (part-11 chain)
For your agents
Use it from Claude, Cursor, or your own agent.
Connect our MCP server and ask for a cited feasibility verdict in plain language. Citations and audit hash included.
Connect the MCP server →Design partners
Onboarding a small group of design partners.
These slots are placeholders — we won't show a logo until a partner has agreed to be named.
Protocols scored in private beta: — placeholder —
Pricing
Per-protocol or annual. No per-seat.
Pay per feasibility run, or go annual for unlimited protocols across your team.
FAQ
Questions, answered honestly.
See a verdict you can actually check.
Send us a protocol. We'll return a fully cited feasibility verdict you can trace, line by line, back to public data — yours to white-label, defend in a bid, or hand to a regulator.