Built to be trusted, and to be checked.
EMME drafts, you decide. Everything below is how that stays safe, evidence-grounded, and defensible, wherever you practise.
Every protocol, checked for interactions, worldwide.
A dedicated Safety agent reviews each protocol against the patient’s own medications, conditions, allergies, and pregnancy status, and flags contraindications and drug–supplement interactions with clear severity tiers.
An interaction is the same pharmacology in every country, so it works wherever you practise, and names your local regulator to verify against.
Every claim carries its working.
Tier & confidence
Each claim is graded 1A → X and carries a 0–100 confidence, so the strength of the evidence is always visible.
Dissent, not consensus
Where reputable sources disagree, the disagreement is stated, never smoothed into a false consensus.
Honest lines
Studied is not proven. Traditional use is not trial evidence. AI-synthesised is not governed. EMME never conflates them.
A recorded sign-off, not a watermark.
- ✓A recorded sign-off, not a watermark. Export and patient-sharing are blocked until you sign.
- ✓Sign-off captures who signed, when, and the exact text approved, an immutable snapshot.
- ✓An append-only audit of the whole chain: data in, AI output, review, sign-off, share.
- ✓When reference data changes, signed protocols are flagged for re-review, nothing shifts silently.
- ✓Every claim carries its evidence tier and confidence, and disagreement is surfaced, never smoothed.
- ✓Patient identifiers never leave EMME for the evidence engine.
Built for patient-data law, across borders.
Per-clinician row-level isolation, encryption in transit and at rest, an append-only audit log, a versioned consent ledger, and a de-identification boundary to the evidence engine. Real patient data is gated on signed agreements (including BAAs) and a completed risk assessment.
Bring the evidence. Keep the judgment.
Run your first case end to end and see the record it leaves.