Product · Roadmap
Medication records (eMAR)
Medication records are the one part of a care platform that can hurt someone if built early and badly. Kindround ships them last, with a clinical safety case, not a shortcut.
Medication records ship in phase 3 with a clinical risk assessment signed off with your registered manager, and a parallel paper run before cutover.
What will ship
Medication list with schedule, dose, route and form; per-visit medication due checklist; outcomes of given, refused, not required, unavailable and self-administered; PRN with reason and effect; missed-dose alerts; MAR chart view and print per person per month.
Controlled drug register with witness sign-off and pharmacy feeds are later, and interaction warnings only through a licensed drug database, never home-grown.
How it is made safe
A DCB0129-style hazard log names the specific hazards: wrong person, wrong dose displayed, stale offline data, silent sync failure, alert not delivered. Each mitigation maps to a requirement, and a change to that requirement reopens the hazard.
A named clinical reviewer from the provider signs the hazard log before go-live.
A parallel paper run of at least four weeks; cutover needs two consecutive mismatch-free weeks and the registered manager's recorded sign-off.
The staleness gate is a floor, not a preference: no configuration can disable it, only tighten it.
See Kindround on a real round, on your own visit types and funders.