Trust
Clinical memory deserves clear controls and honest limits.
Aira is being designed to make consent visible, keep access purposeful, and leave the approved clinical record under doctor control.
Consent
Patients should receive a plain-language explanation before recording and retain the ability to decline.
Encryption
Production data will use encrypted transport and managed encryption at rest. Final technical controls will be documented before deployment.
Access control
Only authorized people should access consultation content, according to their role and the agreed clinic workflow.
Retention
Pilot participants will receive a defined retention schedule. Website pilot applications are retained for up to 12 months.
Deletion
People can request deletion through the published privacy contact, subject to applicable legal and clinical record obligations.
Auditability
Important actions such as access, review, approval, and deletion should be attributable and available for review.
Doctor approval
A machine-prepared draft is not treated as an approved clinical record until the doctor has reviewed it.
Aira does not currently claim certification or compliance with a specific healthcare standard. Those claims require completed legal, security, and deployment review.
Patient clarity
Consent should be understood, not buried.
The person being recorded should know what the recording is for, who can access it, what happens if they decline, and how to ask questions about their information.