Development partners
Become Safer-Med’s clinical development partner.
Built to deploy. Designed to prove its incremental value in real care.
We’re seeking one or two U.S. health-system development partners to validate Safer-Med
on your own data and in your own workflows. Each phase is jointly evaluated before the
next begins — and no nurse receives a notification until the relevance and the
alert burden are acceptable to you.
It takes two champions: pharmacy owns the cabinet, the override governance, and the
clinical logic; nursing owns the moment the dose reaches the patient. Both shape what
Safer-Med surfaces, when it fires, and how it reaches the floor, with clinical
informatics helping design the integration, routing and technical acceptance criteria
— see the view for
pharmacy leadership,
nursing leadership, or
clinical informatics.
Phase 1 · Retrospective
What your workflows missed
We run on roughly 12 months of your historical clinical and ADC data and show your medication-safety committee which clinically meaningful risks Safer-Med would have surfaced — measured as findings not already identified or acted on by your existing safeguards, using comparator data and clinician adjudication. Targeted override triage prioritizes review; it never replaces required override governance.
Gate you agree on: does the signal justify a prospective evaluation?
Phase 2 · Shadow mode
Measured before anyone is paged
Safer-Med runs on live feeds with no nurse paged, measuring adjudicated relevance, alerts per 1,000 dispenses and per nurse per shift, processing latency, and routing readiness.
Gate you agree on: are performance and the expected workflow burden acceptable?
Phase 3 · Graded go-live
Reversible, unit by unit
Activate one unit at a time — reversible at any point — under joint pharmacy, nursing and informatics governance, evaluating actual nurse response, escalation, and clinical utility.
Gate you agree on: should deployment expand?
You shape the thresholds, wording, workflow and evaluation criteria, co-generate the
evidence, and hold named reference rights (with veto) and preferential founding-partner
terms. Every stage is reversible and proceeds only by mutual agreement.
We start with a short conversation to establish clinical value and fit — then, if it makes
sense, a joint pharmacy & nursing workshop to plan an evaluation. No commitment to later phases
is required to begin.