Consultation memory for doctors

Your consultation memory, ready when the patient returns.

Aira captures a consultation with consent, prepares a structured draft for doctor review, and brings the approved context back at the next visit.

Concept render. Final product may vary.

Concept render of the compact black Aira recorder beside pale limestone
01Consent-first capture

Recording starts only after clear patient consent.

02Doctor-reviewed records

The doctor reviews and approves each structured draft.

03Clinical boundaries

No autonomous diagnosis or prescribing.

What is Aira?

A doctor-controlled AI consultation memory system.

Aira is a pilot-stage system for doctors and clinics. With patient consent, the intended workflow captures a consultation, prepares a structured draft, and lets the doctor review, correct, and approve it before the context is reused.

Aira does not diagnose, prescribe, or replace clinical judgment. Product capabilities described on this website remain subject to pilot validation, legal review, and clinical review.

The current problem

The visit moves quickly. The context should not disappear.

Clinical work depends on details, but the normal rhythm of a busy practice makes those details difficult to capture and retrieve.

01

High consultation volume

A full clinic day leaves little room for detailed notes between patients.

02

Fragmented documentation

Context can sit across paper, memory, messages, and disconnected systems.

03

Thin return-visit context

The reason behind a past decision is often harder to recover than the decision itself.

04

Work after clinic hours

Important documentation can spill into the time doctors need to rest.

How Aira works

One responsible path from conversation to continuity.

The workflow keeps the doctor in control at each point where clinical meaning is created or reused.

01

Consent

The doctor explains recording and confirms the patient agrees.

02

Capture

One clear action begins the consultation recording.

03

Secure sync

The consultation moves to the review app when a connection is available.

04

Structure

A draft groups the details that matter for follow-up.

05

Doctor approval

The doctor reviews, corrects, and approves the record.

06

Return visit

Approved context is ready when the patient comes back.

Visible device states

Quiet in the room. Clear when it matters.

A compact e-paper display and a single illuminated control communicate what the recorder is doing without turning the consultation into a screen-led experience.

These states describe the intended pilot experience. Final hardware behaviour will be validated before clinical deployment.

READY

The device is available and waiting for a doctor to begin.

Structured record

A draft built for review, not blind acceptance.

Aira groups consultation context so the doctor can find, correct, and approve the important details.

RETURN VISIT CONTEXTDOCTOR APPROVED
Concerns and symptoms

Patient-reported concerns, timing, and changes discussed during the consultation.

Clinical context

Relevant background and observations documented for the doctor to verify.

Medication and care

Medication and care details as stated, with no autonomous treatment recommendation.

Follow-up actions

Next steps agreed in the room, prepared for confirmation before they become part of the record.

The return visit

Remember the thread, not only the last line.

Aira is designed to make approved context easier to retrieve when a patient comes back, while leaving interpretation and clinical decisions with the doctor.

The concern is explored

The consultation is captured with consent. A structured draft is prepared and reviewed by the doctor.

The record becomes reliable context

Corrections and approvals preserve what the doctor considers meaningful.

The approved story is available

Past context is presented for reference. Aira does not produce an autonomous diagnosis or prescription.

Device and review app

Made to support attention, not compete for it.

The dedicated recorder offers one-button operation, visible status, and local storage. The secure review app is where the doctor examines the structured draft and approves what can be reused.

Warm editorial still life with a notebook, pen, and ceramic cup

Three perspectives

A responsible system has more than one user.

Doctors, clinic teams, and patients experience consultation recording differently. The product and the pilot need to respect each perspective.

Doctor perspective

Stay present, then review the record.

Aira is designed to capture the consultation with consent, prepare a structured draft, and keep the doctor responsible for the final clinical record.

Trust by design

Useful memory starts with clear boundaries.

Consent

Recording begins only after the patient receives a clear explanation and agrees.

Access

Access should be limited to the people responsible for the patient and the approved record.

Retention

Pilot policies define how long recordings and records are kept.

Deletion

Requests are handled through a published privacy contact and a documented process.

Auditability

Important actions should be visible and attributable to authorized users.

Doctor approval

A structured draft is not the final clinical record until the doctor reviews it.

Clinical pilot

Help shape a more useful consultation memory.

We are inviting qualified doctors and clinics in Chennai, Bengaluru, Hyderabad, Mumbai, and Coimbatore to explore the pilot. Applications from other cities join our future-access list.

Frequently asked

Clear answers before the first recording.

Does Aira diagnose or prescribe?

No. Aira is designed to support consultation capture, structured drafting, doctor review, and later retrieval. Diagnosis, prescribing, and treatment decisions remain with the doctor.

Does a patient have to agree to recording?

Yes. The intended workflow starts with a clear explanation and patient consent. A patient can decline without losing access to the consultation.

Is the product available today?

Aira is at the prototype and pilot preparation stage. Product renders and described capabilities are concepts until they are validated in the pilot.

What will the pilot measure?

The pilot is intended to examine workflow fit, consent clarity, review effort, record usefulness, and safe use in real clinical settings. Final measures will be agreed with participating clinicians.