Industries · Healthcare

Clinical conversations, fully reviewed.

Multi-clinician case conferences, M&M reviews, and patient-safety meetings need a record that survives scrutiny. Felarity provides it under a BAA.

Felarity is decision support, not clinical decision support. We do not diagnose, recommend treatment, or substitute for clinician judgment. We give your clinical teams a faithful, attributed, signed record of what was actually said in the room.

What clinical teams use Felarity for

Healthcare organizations operate on a continuous stream of high-stakes conversations. Most leave no usable record. The ones that do are usually scribbled notes that nobody trusts a year later when the case is being re-litigated. Felarity sits in those rooms and produces a record that holds up.

The Healthcare council

When you run a case conference or an M&M through Felarity, four specialist analysts review the transcript independently. Each writes in their own voice; a synthesis layer reconciles them into a final intelligence report. You see all four perspectives — disagreements included.

HIPAA posture

Healthcare is a regulated environment and our posture reflects that. We do not ask clinical leaders to take our word for any of this — every line below maps to a control documented in /trust/compliance/.

What Felarity is not

We want this on the page in plain language because clinical leaders ask it on every call. Felarity is not an EHR. We do not write to your chart. We do not replace your documentation workflow. Felarity is not a clinical decision support system in the regulatory sense — we do not diagnose, do not recommend treatments, and do not produce outputs intended to direct patient care. Felarity is not a substitute for clinician judgment. Everything the council produces is decision support for the people in the room and the people who review the room afterward. The clinicians remain the clinicians.

Workflow example

A typical deployment for a hospital quality department looks like this:

  1. Sign the BAA and provision a PHI-flagged workspace for the patient-safety committee. Retention is set to ninety days for audio, indefinite for signed reports.
  2. Record case conferences and M&M sessions through the meeting capture. Diarization separates speakers in real time. Live contradiction detection runs against the clinical council during the session.
  3. On stop, the eleven-stage post-session pipeline runs: concatenation, full-session diarization, acoustic markers, confrontation classification, speaker attribution, NLI re-scoring, topology analysis, deep council re-analysis, and the 8-node Merkle attestation chain.
  4. Review the report through the Clinical Risk Officer persona for safety posture, then the Quality Improvement Lead for process findings. Both write in their own voice and cite the transcript moments they are referencing.
  5. Export the signed report for the patient-safety committee file. The Ed25519 signature and Merkle root are embedded; the public verify endpoint at /verify/ lets any reviewer confirm the record was not altered.
A note on what this replaces

Most clinical committees today operate on a handwritten note, a Word document drafted three days after the meeting from memory, and an action item list nobody quite remembers agreeing to. Legal teams typically report that the gap between what was said in the room and what ends up in the file is where preventable risk lives. Felarity closes that gap.

Request a BAA Talk to clinical lead

Last updated: June 7, 2026.