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Frequently asked questions

Straight answers to the questions sponsors, sites, and investors ask us most. Something missing? Contact us and we'll answer directly.

What is Eichor?

Eichor is a software platform for clinical research intelligence. It brings together public registry, regulatory, and payment data and turns it into insights that teams can act on: site-risk grades, results-disclosure compliance, protocol feasibility and competitive trial landscapes.

Where does the data come from?

The data comes from public, authoritative sources: ClinicalTrials.gov, the EU CTIS register, UK MHRA requirements, NIH RePORTER, CMS Open Payments, FDA inspection and enforcement records, and SEC filings. Every claim in our deliverables links back to its source.

Do you use patient data or PHI?

No. Eichor works only with public, institution-level data such as trial registrations, disclosure records, and aggregate payments. We never handle or access patient records, electronic health records, or any form of PHI.

How does Eichor use AI?

Eichor uses AI mindfully, and never as a unilateral source of facts. Every data point comes from structured pipelines built on public sources — the same query always returns the same result, with clear source attribution. AI operates on top of this verified data: it interprets, explains, and identifies inconsistencies across sources. The intelligence is AI-assisted; the evidence is always grounded in source data.

How do I know the analysis is reliable?

In two ways most vendors don't offer. First, key facts are sealed in a signed, tamper-evident ledger at the moment they are generated. Second, we keep a verified track record: our at-risk queries are checked against actual registry outcomes, and misses are published alongside hits.

Who is Eichor for?

Eichor is designed for sponsor and CRO clinical operations and feasibility teams; research sites seeking accurate representation of their performance; business development teams; investors and vendors tracking clinical trial activity; and academic institutions.

What does it cost?

There is a free tier — the same-day Site-Risk Snapshot and sample digests — and paid options ranging from one-off reports to annual subscriptions and enterprise portfolio coverage. See the pricing section on the home page, or request a quote for enterprise needs.

Can I try it before buying?

Yes. Run a free Site-Risk Snapshot, review sample reports, or request a demo. Every paid product has a sample you can review before paying.

How do I get access?

Use the Request Access form. We review submissions and onboard new users by email. Sign-in uses one-time email codes, so there are no passwords to manage.

Do you integrate with our internal systems?

The core product runs in the browser with exportable reports, so there is nothing to install. For enterprise engagements, we scope integrations (HL7 FHIR R4, CTMS and EDC data flows) case by case.

Is our usage confidential?

Yes. The site sets no cookies and uses no third-party trackers. What your team searches and unlocks is never shared or sold. Enterprise engagements run under NDA.

Can consultants resell or white-label Eichor?

Yes. Through the partner program, consulting firms deliver Eichor-generated evidence under their own brand at partner rates. See the Partner Program page.

Planning or rescuing a trial? Eichor generates evidence-linked site-risk reports from public data in minutes. Get a free preliminary snapshot →
Launch offer through July 31: first full site unlock free — one per company.