Upload VCF data, select medications, and receive CPIC-aligned risk insights with actionable recommendations. Built for safety, clarity, and real-world clinical workflows.
Dual-audience summaries for clinicians and patients, grounded in the evidence.
Dose and therapy recommendations mapped to recognized guidelines.
Clear status, confidence signals, and export-ready results.
Evaluate multiple drug risks to surface interaction and safety concerns.
A transparent pipeline clinicians can trust.
Securely ingest a VCF file with local validation and privacy-first parsing.
Extract pharmacogenomic markers (genes, rsIDs, star alleles) from INFO fields.
Translate diplotypes into clinically meaningful phenotypes.
Apply CPIC-backed logic to classify risk and dosing guidance.
Generate clear clinical and patient summaries with AI assistance.
Return structured results for export, sharing, or audit.
PharmaGuard bridges the gap between complex genomic data and bedside decisions. It pairs a deterministic risk engine with AI-generated explanations to help clinicians act confidently while keeping patients informed.
Supports core pharmacogenes and high-impact medications with confidence scores.
Outputs shareable JSON reports for clinical documentation.
Privacy-first workflow: data stays local until analysis submission.
PharmaGuard is designed to assist clinical decision making, not replace it. Always validate against institutional policy and current CPIC guidelines.
Launch the analysis workspace and get risk results in minutes.