The questions that stall deals.

Three things, from one supply of verified doctors. Grade your AI: clinicians score your model’s answers and show you where it fails. Data, made to order: recordings, interviews and clinical Q&A collected fresh to your spec. Continuous supply: a dedicated cohort producing every month under a standing contract. Most clients take all three.

Feasibility on any cohort, with counts, within 48 hours. The 24-hour test returns first responses to a structured question within a day of go. Custom recordings start in days and first files land in four to eight weeks.

You send one real question, we put it in front of verified clinicians in our own community, and first responses come back within 24 hours. It is the cheapest and fastest way to judge us. How the test works →

Yes. If the data doesn’t exist, we record it: your specialty, your language, your topic, audio or video, consent attached. Composing a cohort and fielding it is what this team did more than 1,200 times last year.

No. Every engagement is scoped to a bench, a language set and a volume, so numbers are discussed on a call once we have confirmed feasibility. Nothing on this site is an offer.

A named human replies within one business day. For the catalogue, a mutual NDA arrives first and the catalogue follows the same day it is signed. For the 24-hour test, we confirm the bench and take your question. For partner terms, we set up a short call.

Four explicit affirmations, signed before the session and timestamped: recording, processing, licensing, and use as AI training data. Withdrawal applies to future use. Older collections are re-consented before any licensing, and each collection’s consent status is stated plainly in the catalogue.

One signed page per file: consent scopes, credential verification and the method used, the collection record, and chain of custody. One ID, one signature, verifiable on audit.

No. You receive professional attributes only: specialty, country, experience band. Identity stays in our custody, verifiable on audit, never attached to a file. Redaction runs to a versioned key.

EU GPAI enforcement has been live since 2 August 2026, with public training-data summaries required and fines up to €15M or 3% of turnover. Every FieldTruth file ships with signed consent and a provenance certificate, which strengthens your compliance file. This is documentation, not legal advice.

No, and we say it unprompted: data from commissioned research is never licensed, resold, or used to train any model, warranted in writing. FieldTruth material is collected separately, under purpose-scoped consent.

Yes. Audit trail on demand, identities verifiable on audit, and a named human who answers the same day. We are certified to ISO 27001:2022 and ISO 20252:2019 and are corporate members of ESOMAR, Intellus Worldwide, EPHMRA, BHBIA and AQR.

Never without consent, and never identifiable. Where a commissioned project records real doctor–patient encounters, both the clinician and the patient consent explicitly before recording. Every file is de-identified before licensing; patient identity never enters a dataset and remains in our custody. We do not collect patient medical records — case data is physician-abstracted.

Pipeline-ready data in one audio standard, native and English transcripts, diarised JSON, a metadata sheet per file (duration, sample rate, specialty, country, counts, accuracy, redaction key) and a provenance certificate per file.

In a locked room: named users, streamed media, no downloads, access that expires with the licence. One buyer, one room.

Yes. The catalogue lists what exists, what is weeks away and what we build to order. It is shared under NDA. Request the catalogue →

Committed buyers get first refusal on new capacity. When demand collides, committed contracts are served first.

A mutual NDA for the catalogue, then an evaluation licence before anything ships, then a plain-language data licence or services agreement. Every delivery passes our compliance gate first, warm relationship or not.

Yes, as commissioned collection. Real consultations recorded at the point of care, with explicit consent from both clinician and patient captured before recording, fully de-identified to a versioned redaction key before delivery. Scoped per specification — tell us the specialty, language and setting.

Twelve and counting, with unusual depth in Hindi, Gujarati and other Indian vernaculars, Spanish (Spain and Latin America), Portuguese, Filipino and English variants. For a Gujarati-speaking diabetologist we are often the only option that exists.

Not in our current language set.

Forty-plus. Primary care at volume; oncology with more than 2,000 members; deep cells in cardiology, endocrinology, neurology, internal medicine, surgery and family medicine; rare disease composed to spec. See the network →

Six layers behind every member: credential capture, OTP, biometric liveness, device and email risk intelligence, human licence QC against official registries, and government ID with face match. Every member is reviewed by our QC team before their first task.

Published honoraria scaled to the work and paid within 30 business days, a specialty-calibrated feed with no noise, and a community that gives back: a peer forum, a journal, webinars. Fairly treated experts answer fast and stay for years.

Yes, under partner terms. You buy output, never access to the panel; no physician identities; white label is allowed, but the provenance certificate always carries GRG Health’s signature. Ask for partner terms →

Yes, the same partner terms apply, and if you already buy research from GRG Health your existing relationship owner stays in the room.

We license small corpora and clinician evaluation for published work and ask for the citation. Ask about a research licence →

Always. Direct lines are here, or use the form and a human replies within one business day.