Medora drafts notes, surfaces the right evidence, and closes care gaps at the point of care — every output traceable to its source and reviewed before it touches the chart. HIPAA-aligned, SOC 2 Type II, and built to keep clinicians in control.
Medora works across the visit — before, during, and after — so documentation, evidence, and follow-up stop competing for your attention.
Turns the patient conversation into a structured, specialty-aware note in under 30 seconds. SOAP, H&P, or your template — drafted, never auto-filed.
Answers clinical questions with guideline-grade citations from peer-reviewed literature and your own protocols. Every claim links back to its source.
Flags overdue screenings, drug interactions, and risk signals from the chart in real time, mapped to HEDIS and your quality measures.
Nothing reaches the record without a one-tap clinician sign-off. Edits train your team's preferences, not a public model.
Bi-directional sync with Epic, Cerner, and FHIR R4 endpoints. Notes, orders, and codes land where your team already works.
Every suggestion carries a full trail — model version, source, prompt, and reviewer. Built for compliance, not guesswork.
What care teams see in the first 90 days
Medora is modular. Roll out what your team needs today and add capabilities as trust builds.
Summarizes the chart, prior visits, and open issues into a 20-second briefing so clinicians walk in ready.
Listens with consent, ignores small talk, and structures the encounter into your preferred note format live.
Suggests ICD-10 and CPT codes with supporting evidence, and queues orders for clinician approval.
Generates a plain-language after-visit summary at a 6th-grade reading level, ready to translate into 30+ languages.
Produces SBAR handoffs and referral letters that carry the full clinical context, not a copy-paste blob.
Rolls up quality measures and documentation health across panels — de-identified and governed by role.
“I used to chart until 9pm. With Medora I finish notes before I leave the building — and they read like I wrote them, because I reviewed every one.”
“What sold our compliance team was the audit trail. Every AI suggestion is sourced and signed off. We passed our HITRUST review without a single finding tied to Medora.”
“The care-gap radar caught a missed mammogram reminder on a patient who'd slipped through three visits. That's not efficiency — that's a better outcome.”
Every plan includes a signed BAA, SOC 2 Type II controls, and clinician-in-the-loop review. No PHI is ever used to train shared models.
For independent clinics and small groups.
For multi-site groups and hospitals.
For IDNs and payers with complex governance.
Yes. We sign a Business Associate Agreement with every customer, encrypt PHI in transit and at rest, and operate under SOC 2 Type II and HITRUST-mapped controls with full audit logging.
No. Patient data is never used to train shared or public models. Your clinicians' edits tune preferences within your own tenant only, and data is logically isolated per organization.
Never automatically. Every note, code, and order is a draft until a licensed clinician reviews and signs off. Medora keeps the human in the loop by design, not as an afterthought.
Medora connects to Epic and Cerner via bi-directional sync and to any FHIR R4-compliant system. Most integrations are live within four to six weeks, including validation.
Every evidence response is grounded in peer-reviewed literature and your own protocols, with inline citations you can verify. Medora declines to answer rather than guess when the evidence is thin.
A single-clinic pilot can be running ambient notes in days. Full health-system deployments with EHR sync typically go live in four to eight weeks, including security review.
See Medora draft a real clinical note from a sample encounter — and review the audit trail behind every suggestion.