Medical
Clinical evidence, genomics, pharmacology, oncology, and rare disease — ingested from 143 authoritative sources, cross-validated, and calibrated. Nine products live across medication safety, drug discovery, clinical evidence, genomics, and more.
Available now
Skippy Ground
Claim VerificationVerify any medical claim against Skippy's evidence base. Returns a calibrated confidence score, source citations, and surfaces contradictions. The evidence verification layer for healthcare AI.
Skippy Auth
Prior AuthorizationEvidence-grounded prior authorization intelligence. Given drug + diagnosis, returns a fully auditable recommendation with source lineage — defensible to CMS.
Skippy Variants
GenomicsGenomic variant interpretation with ACMG/AMP criteria applied programmatically. Built on 2.8M ClinVar records. Continuous monitoring for reclassification-warranting evidence changes.
Skippy Med-Check
Medication SafetyMedication safety intelligence for health plans, PBMs, and consumer health apps. Drug interactions, side effect attribution, and pharmacogenomics — grounded, not hallucinated.
Skippy Rare
Rare DiseasePhenotype matching, variant evidence, natural history synthesis, and trial intelligence in one platform. 300M people have rare diseases; 90% wait years for a diagnosis.
Skippy Integrity
Clinical Fraud PreventionPre-payment clinical plausibility screening for Medicaid and Medicare fraud detection. Evidence-grounded claim and regimen verification with OIG-ready audit records.
Skippy DDI
Drug InteractionsMechanistic drug-drug interaction analysis grounded in pharmacology evidence. CYP enzyme, transporter, and QT prolongation interactions with CPIC-aligned clinical action guidance.
Skippy Clinical
Clinical Decision SupportReal-time order verification, treatment protocol guidance, and discharge summary review — FHIR R4 native, CDS Hooks compatible, evidence-grounded at every step.
Skippy Pharmacogenomics
PharmacogenomicsGene-drug interaction guidance for 24+ actionable gene-drug pairs. CYP2C19, CYP2D6, DPYD, and TPMT clinical action recommendations — CPIC and PharmGKB aligned.
Skippy Pharmacovigilance
Drug SafetyCross-validate adverse event signals across FAERS, OnSIDES, and VAERS against pharmacology evidence. Detect emerging safety signals months before label updates.
Skippy Drug Discovery
R&D IntelligenceDrug repurposing intelligence grounded in ChEMBL, pathway data, and clinical evidence. Identifies novel indications with calibrated confidence and tamper-evident prediction records.
Skippy Biomarker
Biomarker AnalysisBiomarker validation across genomics, expression, and clinical evidence sources. FDA/EMA qualification status, companion diagnostic alignment, and trial enrollment correlation.
Skippy Trial Design
Clinical TrialsPatient matching, endpoint analysis, and site selection for clinical trials. Searches 578K+ ClinicalTrials.gov records with eligibility matching and investigator identification.
Skippy Medical Coding
Medical CodingPre-submit CPT/ICD-10 verification against NCD/LCD coverage policies. Evidence-grounded denial prediction and appeal support before claims go to payer.
Skippy Pharma Compliance
Pharma MarketingFDA off-label claim detection, fair balance scoring, and evidence verification for promotional materials — before MLR submission, before OPDP enforcement.
Skippy CDSS Marketplace
CDS RulesPre-built, evidence-calibrated clinical decision support rules deployable to Epic and Cerner via CDS Hooks. Browse, customize, and deploy validated rules in hours.
In development
Skippy Mind
Behavioral HealthPsychiatric medication safety, pharmacogenomics for mental health drugs, serotonin syndrome detection, and QT prolongation risk — for digital mental health platforms and behavioral health EHRs.
Skippy Reimbursement
Coverage & ReimbursementMulti-payer coverage reasoning across Medicare NCDs/LCDs, 50-state Medicaid, and top-30 commercial payer medical policies. CONTESTED detection, appeals strategy with cited ALJ/QIC/DAB precedent, DRG/APC classification, and NCCI screening.
Skippy Embedded CDS
White-Label CDSRegulatory-grade clinical decision support in a white-label SDK — for carriers, telehealth platforms, PBMs, and retail health. Bypasses EHR gatekeeping. Per-segment compliance adapters, member-facing tone calibration, and Article 14 enforcement built in.
Skippy Outcomes Eval
Clinical OutcomesFDA-deliverable outcomes evidence for healthcare AI companies. Pre-registered IRB-ready protocols, 50+ board-certified reviewers, pre-validated statistical pipelines, and FDA SaMD-formatted output — at 60–80% of the cost of building from scratch.
What we ingest
Every source is ingested, normalized, and cross-validated. Provenance is preserved at every layer — nothing is a black box.
“50–90% of medical AI responses are not fully supported by their own cited sources — sometimes contradicted by them.”
Stanford SourceCheckup, Nature Communications, Apr 2025 · 800 questions × ~58K statement-source pairs across 7 LLMs
Skippy's verifier rejects ungrounded output as a hard contract. The citation target is a verified finding with calibrated confidence and full source lineage — not a paper, chunk, or URL.
Embedded in your EHR — not alongside it
Skippy integrates at the point of care via CDS Hooks — the HL7 standard for real-time clinical decision support inside EHR workflows. Clinicians receive evidence-grounded alerts without leaving their chart.
Surface pharmacogenomic alerts, contraindications, and missed screening recommendations as a clinician opens the patient record.
Drug–drug interaction checks, pharmacogenomic dosing guidance, and evidence-grounded alternatives at prescribing time.
Evidence-based appropriateness checks at order entry — flag duplicate tests, off-guideline orders, and high-risk combinations.
See Skippy in your clinical workflow
We work with health systems, life sciences companies, and clinical informatics teams. Let's talk about your evidence problem.
Request a Demo