HarnessHealth

Start a pilot

Put a named physician
behind your AI output.

Your model drafts the prior-auth determination, the letter, the coded note, the answer to the patient. A licensed, NPI-verified physician signs it, revises it, or declines it with a reason — and you get a receipt anyone can verify. The law increasingly requires the human; we supply the human and the record.

Pre-go-live pilot. The sandbox runs synthetic samples in your browser and stores nothing. A BAA is offered to qualifying covered entities; none has been executed yet.

What every output gets

  • A named reviewer. A physician verified against the CMS NPPES registry, matched to the specialty of the output, bound to a signing key only they hold.
  • A real decision. Sign, revise, or decline — with a documented rationale. The fee is the same either way, so the no stays honest.
  • A receipt. NPI, timestamp, and document hash, anchored on hashcare.com and countersigned daily. Verifiable by anyone, without asking us.
  • A closed gate. Outside a covered specialty the gate fails closed and tells you so. It never quietly approves.

Price

$12 – $100

per review, a flat fee by document class — the same whether the physician signs or declines. The platform fee is flat per completed review and disclosed before you accept. No subscription, no checkout here; rates are published on clinicalswipe.com.

  • Sandbox: free. Synthetic or de-identified outputs only.
  • Production: the per-review fee above, with terms that follow a BAA.
  • Never: a share of your revenue, a fee tied to approvals, or a fee tied to referrals.

Flat fees regardless of outcome are the structure the HHS Office of Inspector General viewed favorably in Advisory Opinion 25-03 (June 2025). That is a design principle here, not a legal opinion about your arrangement.

Why a vendor needs this now

CMS's WISeR model, running from January 2026 in six states, requires that every non-affirmation be reviewed by a human clinician with relevant expertise and that no denial be made solely by technology. Seven states passed laws in 2026 saying the same thing to insurers: AI may draft or screen, but a licensed human makes and signs the adverse decision. If your product feeds one of those decisions, the human is now a requirement, not a feature.

Most of those laws bind the plan, not the vendor. A vendor selling into a plan supplies the clinician the plan must have — and the record that proves it. Whether a given arrangement satisfies a given statute is a question for the plan's counsel; we supply the named, licensed, specialty-matched reviewer and the receipt.

The other reason is cost. Mayo Clinic's chief AI implementation officer told Becker's (August 31, 2026) that the cost of maintaining AI systems is “far higher than I think any of us in the industry really thought,” and that his engineers can never let go of a live product. A flat fee per review turns the human part of that burden into a variable cost. The numbers →

The statutes, the dates, and the sources →·Built for a WISeR participant? →

Request a pilot.

Five fields. The founder reads every one. If the answer is not yet, you will be told what has to be true first.

Your request reaches the founder directly. The sandbox is open now; no patient data until a BAA exists.