Patient command center
Single-pane patient profile that unifies medications, labs, PGx, wearables, phenotype, and timeline into a clinician-readable chart.
Genomic, lab, medication, wearable, phenotype, and EHR signals — unified into a clinician-readable chart and surfaced as the small set of decisions that actually matter for today's visit.
PrecisionRx AI is the explainable precision-medicine decision-support layer that plugs into the EHR a clinic already uses. It organizes patient-specific clinical data into a structured context, runs evidence-linked decision-support modules against that context — starting with pharmacogenomics and drug safety — and surfaces cited recommendations for a licensed clinician to review and approve.
PrecisionRx AI is decision support. It does not diagnose, prescribe, or act autonomously. The clinician makes every clinical decision.
Every module routes back to the same versioned rule engine and audit-logged review surface. Adoption can start with a single lane and expand without re-platforming.
Single-pane patient profile that unifies medications, labs, PGx, wearables, phenotype, and timeline into a clinician-readable chart.
CPIC- and PharmGKB-aligned phenotype calls with versioned evidence. Drug-gene safety surfaces only when the data quality clears the bar.
Lab + IVD normalization into FHIR-ready DiagnosticReport / Observation context with LOINC, source provenance, and quality grading.
ApoB / Lp(a) / HbA1c / lipid / CGM trends interpreted with statin tolerability, renal function, and pharmacogenomic context.
Sleep, HRV, resting heart rate, and CGM trends correlated to medication initiation events. Catches side-effect signals before the next visit. Wear-time confidence and stale-feed gating built in.
Rare-disease feasibility, suspected mechanism, candidate categories for specialist review, and a missing-data checklist.
Intake, evidence, visit-prep, report, referral, care-gap, and patient-explanation drafts. Model + prompt versioning. Drafts only.
Co-sign workflows, suppression, amendment, hash-chained audit log, quality-override governance, and rule-version snapshots.
Clinician PDF, EHR paste block, patient-friendly summary, and specialist referral templates. Provenance snapshot per report.
A composable pipeline that keeps the clinician at the keel. Every stage is auditable, versioned, and reversible.
EHR, labs, PGx vendors, sequencing partners, wearables, patient questionnaires, PDFs.
SMART-on-FHIR, HL7 v2 / FHIR R4, VCF, CSV, OCR. Source-tagged with provenance.
FHIR-shaped Patient / Medication / Lab / Variant / Phenotype / Timeline records.
Versioned CPIC / PharmGKB / FDA-label / guideline entries with aging review queue.
Deterministic specialty-laned rules. Categories: safety, efficacy, monitoring, optimization.
Intake / evidence / visit prep / report / referral / patient-explanation drafts.
Lifecycle states, required rationale, supervising-clinician co-sign on prescribing-relevant accepts.
Clinician PDF, EHR paste, patient summary, specialist referral. Source-data snapshot per report.
Switch the lane and the panel composition, default rules, and report templates reshape themselves. Same evidence backbone, different daily surface.
PGx medication safety
Cardiometabolic optimization
Psychiatry medication review
Renal / hepatic monitoring
Medication tolerability monitoring
Rare disease feasibility
Polypharmacy review
Preventive + longevity
No proprietary data shapes for clinical concepts. Imports validate against industry vocabularies; exports return them.
Open a sample patient — Jane Smith, 38F, three high-priority items waiting — and walk through the workflow without scheduling anything.