How it works
Study in. Cited verdict out. In hours.
No black-box scoring, no weeks waiting on a vendor. Describe the study and get a six-pillar assessment where every number links to its public record — ready to verify, defend, and act on today.
Describe → gather evidence → six-pillar assessment → signed deliverables.
The four steps, in detail
What happens between upload and decision
Each step is built so anyone in the room — clinical, commercial, or financial — can trace the result end to end.
You describe the study
Upload the protocol PDF, or start from just the molecule (or drug class) and the indication — enough for a full public-data assessment even before a protocol exists. The platform reads out the indication, intervention, phase, endpoints, and eligibility criteria. Your documents are processed privately and are never used to train a model.
The engine gathers the public evidence
Around 50 live public sources are pulled for your study: ClinicalTrials.gov and national trial registries across the world, PubMed and preprint literature, FDA and EMA regulatory precedent, pharmacology and target databases, patents, drug pricing, and SEC filings. Every record is pinned to the exact snapshot it was read from, and the evidence ledger shows honestly which sources returned data — and which didn’t.
Six pillars, one verdict
More than 30 analyses are computed across six pillars — scientific rationale, trial design, patient cohort, sites & cost, commercial case, and the verdict itself — ending in a go/no-go recommendation. Every number carries its citation, an honest evidence grade, and the whole run lands on a tamper-evident audit trail aligned to 21 CFR Part 11.
Expert roles turn it into deliverables
Seven expert workspaces — protocol design, biostatistics, clinical pharmacology, commercial strategy, and more — draft the documents your decision needs: a Go/No-Go memo, a protocol synopsis, a statistical analysis plan, valuation scenarios. Your team reviews and approves each one with a Part 11 electronic signature; if the underlying evidence later changes, the signed decision is flagged for re-review.
Why cited matters
A verdict you can hand to a board, a sponsor, or a regulator
The output is not an opinion — it is a defensible argument.
Every figure in the assessment — probability of success, eligible-patient reach, site density, budget band, market size — carries a citation back to the exact public record it was derived from, along with the query and the snapshot date. Open the citation on any number and you see the source, so your team can confirm the claim independently rather than trusting a model.
The assessment is also honest about what it doesn't know. Every analysis carries an evidence grade — from single-source up to triangulated — and numbers built on thin evidence say so on their face. Because every run lands on a tamper-evident audit trail and every sign-off pins the exact evidence it was based on, a verdict produced today can be reproduced and re-audited months from now. That is the difference between a number you believe and a number you can defend.
See a verdict you can actually check.
Send us a protocol — or just a molecule and an indication. We'll return a fully cited feasibility assessment you can trace, line by line, back to public data — yours to defend in a bid, take to your board or investment committee, or hand to a regulator.