About

Why Authora exists.

The U.S. spent $35 billion last year on the friction between two parties who both want the same outcome. We are the platform built to remove it — without making either side flinch.


The premise

80.7% of appealed denials get overturned.

Source: KFF analysis of CMS Medicare Advantage data, 2023 reporting year. The number has been stable, within two points, every year since.

That statistic — 80.7%— is the founding fact of this company. Read it once and the implications stack up fast. If a payer’s denials are overturned eight times out of ten on appeal, the denials were wrong at issuance. The appeals process is not a check on edge cases; it is the actual adjudication process, run in slow motion, with a patient’s care delayed for the duration. The first decision is not a decision. It is an obstacle whose only job is to filter out the patients who give up.

And most do. Fewer than 12% of denied Medicare Advantage prior authorizations are ever appealed. Multiply that by the overturn rate and the conclusion is uncomfortable: every year, a knowable number of Americans do not get care that, on the evidence, they were entitled to under their own coverage. They did not get it because the friction worked.

We started Authora because that gap is closeable, and because the regulatory window that just opened — CMS-0057-F — means closing it became a contractual obligation by January 1. Payers will have to publish their PA turnaround times, denial rates, and approval-rate-by-procedure category every year. The friction was profitable when it was invisible. It will be considerably less so when the numbers are on a public site indexed by every benefits consultant in the country.

We are not building an AI denial-faster machine. We are building the platform that produces the published numbers, truthfully, and produces them well — because the system underneath is set up to answer the right question at the right moment, with the evidence already attached.


What we believe

Four convictions.

These predate the company. They will outlast the current product surface.

01

PA exists because evidence asymmetry exists.

Payers cannot see the full clinical picture; providers cannot see the full policy library. Prior authorization is the awkward bridge between those two information gaps. Remove the asymmetry — surface the evidence and the policy together, at decision time — and the bridge becomes a transaction, not a months-long negotiation.

02

Denials should be defensible — not faster.

A platform that issues denials faster than the legacy stack is not progress. A platform that issues fewer denials, and the ones it does issue survive appeal at a much higher rate, is. The KFF data on overturn rates is the only honest scoreboard. Authora optimizes for that scoreboard, not the throughput one.

03

The trace matters more than the answer.

Every Authora decision is shipped with the criteria it cited, the policy excerpt, the supporting evidence in the chart, and the reviewer (human or agentic) who signed it. A decision without a trace is not auditable, not defensible, and not eligible for delegated UM. The trace is the product. The answer is a consequence.

04

The regulation is the floor, not the ceiling.

CMS-0057-F sets a minimum. The plans that hit only the minimum will publish embarrassing public-reporting numbers on January 1 and spend 2027 explaining them. The plans that build the system that produces those numbers truthfully — and good — will not have to explain anything. Authora is built for the second posture.


Where we operate

Distributed engineering. PHI in one region.

Engineering

Distributed across the United States. Engineering office in New York City. We hire remote-first; on-site collaboration is concentrated around two- and three-week working blocks.

Data residency

All PHI in us-east-2 (Ohio). No data crosses U.S. borders. Full data-residency posture documented in /trust.

Customer-facing roles

NYC, Boston, Nashville, San Francisco. Clinical operations team distributed across all four U.S. time zones for on-call reviewer coverage.

Legal entity

Delaware C-corp. BAA-ready under the standard OCR template. Counsel of record: a national healthcare regulatory firm; specifics provided in diligence.


The standards we serve

Bodies we are accountable to.

Healthcare interoperability is governed in committee rooms by professionals who have been at this for decades. We participate where it matters and we listen everywhere else.

  • HL7 Da Vinci ProjectPAS, CRD, DTR, PDex
  • X12278, 270/271
  • CMS Office of Burden Reduction & Health InformaticsCMS-0057-F engagement
  • NCQAUtilization Management Accreditation track
  • WEDIStrategic National Implementation Process
  • CAQH COREPhase IV applicant
  • ONCHealth IT Certification Program registrant

Backers

Who we’re building with.

We’re honest about where things stand: production infrastructure partners are listed by name. The healthcare advisory roster is being recruited deliberately through Q3 2026 and we won’t put placeholder humans on this page.

Infrastructure
Anthropic
Model infrastructure partner
Infrastructure
Supabase
Data platform partner
Infrastructure
Netlify
Application infrastructure partner
Advisor seat
Healthcare advisor — TBA
Founding clinical advisor seat, Q3 2026
Advisor seat
Healthcare advisor — TBA
Payer policy advisor seat, Q3 2026
Advisor seat
Healthcare advisor — TBA
Regulatory affairs advisor seat, Q3 2026