What was tested
Deterministic source retrieval, claim-to-source coverage, explicit UNKNOWN/conflict handling, stable manifests, script-free reports and altered-file detection.
Trial Provenance Pack
Give us a public NCT ID. We return a portable evidence pack showing where material trial facts came from, what changed, what conflicts, what remains unknown, and whether the delivered package was altered.
Not an efficacy score. Not a regulatory certification. A provenance layer for consequential trial decisions.
Why trust this enough to spend $2,500?
Deterministic source retrieval, claim-to-source coverage, explicit UNKNOWN/conflict handling, stable manifests, script-free reports and altered-file detection.
The current engine passes 16/16 deterministic tests. Canonical UD regressions remain separate, and every public sample carries an integrity-verified manifest state.
No clinical-truth determination, FDA validation, regulatory certification, GxP or Part 11 claim, verified signer identity, or trusted timestamp is implied.
30-second proof
The sample keeps the public source, retrieval context and claim relationship next to the observation so another reviewer can inspect the path.
Inspect this in the verified sample →Ordinary diligence vs portable provenance
Summary, detached links and analyst context travel separately. The next reviewer reconstructs which source supports which fact.
Material observations, source relationships, explicit uncertainty, delivery manifest and verification artifacts travel together.
Who it’s for
Board, partner and portfolio decisions tied to changing public trial evidence.
Faster reconciliation across registry records, publications and later updates.
An inspectable trail that travels beyond the analyst who assembled it.
A portable public-evidence layer that complements existing controlled systems.
What you receive
Every material field is source-backed, explicitly UNKNOWN, or explicitly in conflict.
A readable, script-free report for reviewers.
Structured trial observations and declared sources.
Material fields mapped to evidence and retrieval context.
A deterministic inventory of the covered delivery.
Files and instructions for integrity and tamper checking.
Compare completed, terminated and withdrawn public trial states. Public-source evidence only; no patient-level data or implied sponsor endorsement.
Completed registry record with exact-NCT publication relationships.
Integrity verified · no recorded conflicts
Open human-readable report →View report, JSON, ledger and manifest →A terminated public record showing why state and provenance matter.
Integrity verified · status remains inspectable
Open human-readable report →View report, JSON, ledger and manifest →A withdrawn trial where no publication relationship is manufactured.
Integrity verified · absent relationships remain UNKNOWN
Open human-readable report →View report, JSON, ledger and manifest →Request → quote → payment → delivery
Submit one public NCT ID, a work email and the decision or review the pack should support.
A person checks public-record availability and sends written scope, exclusions, delivery timing and price.
After you accept the scope, you receive secure payment instructions through the existing commercial service.
Work begins only after confirmed payment. The operator assembles and independently checks the bounded pack.
You receive the agreed artifacts through the confirmed delivery channel, followed by the included readout.
The request form does not collect trial files, patient information, PHI or confidential evidence. Secure handling requirements are agreed before any non-public material is accepted.
Clear pricing
Bounded, operator-assisted deliverables. Universal Document remains the evidence substrate.
One Trial Provenance Pack and a 30-minute readout.
Request this pack →Three packs plus a cross-trial provenance issue summary.
Ten packs plus a portfolio-level provenance summary.
Monitoring for up to ten previously packed trials.
Portfolio Mode
Submit a bounded trial list once. Receive individual provenance packs plus a transparent cross-trial summary—never a mysterious quality or risk score.
Provenance confidence summary
No single percentage is presented as “truth.” The buyer sees the underlying states and evidence.
Trial Provenance Pack does not establish clinical truth, FDA validation, regulatory certification, GxP or 21 CFR Part 11 compliance. It shows the provenance and limits of the public evidence included in the delivered pack.