What patient, reporting, and analytics features did Burna AI ship in 2025 and 2026?

Patient reporting runs through Healthnotes, the trial participant app: a site issues a PRO token that serves as the participant's login, and sponsors compose, schedule and publish instrument batteries, including PRO-CTCAE, without an app release. What a participant reports between visits is carried into the next encounter, where it stays the patient's own report and the clinician grades. A pre-visit interview gathers the coordinator's questions before the visit for verification and sign-off. Reports: FDA MedWatch, IRB and serious adverse event reports are produced from the graded record and download as documents, alongside adverse event report PDFs with WHO-UMC and Kramer attribution. Analytics: grading, rater agreement and PRO submission views, and a sponsor safety surface where a sponsor reads graded data for its own trials, separate from the site view.