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LOINC Pharmacogenomics Codes: A Lab Implementation Guide
Which LOINC codes to use for pharmacogenomics results: the PGx panel, CPIC phenotype answers, gene codes, how LOINC differs from SNOMED CT, and how to map them.
ISO 15189 for Genomics Labs: Accreditation Guide
How ISO 15189:2022 applies to genomic and pharmacogenomic labs: bioinformatics validation, version drift, vendor oversight, data retention and audit readiness.
Cloud Security for Genomics: A Lab Buyer's Guide
How clinical labs should evaluate cloud security for genomic data: HIPAA duties, SOC 2, ISO 27001, disaster recovery, SLAs and NIST threat modeling.
HIPAA BAA for Genomics: What Your Lab Must Require
What a HIPAA business associate agreement must cover when your lab uses genomics or PGx software: required terms, data return, incident reporting and subcontractors.
PGx Software Cost: What Labs Really Pay in 2026
What pharmacogenomics reporting software costs a lab: subscription ranges, one-off integration budgets, and the review and EHR costs that decide your total.
PGx RFP Checklist for Clinical Labs: Make CPIC, CLIA, and FHIR Testable
Build a defensible PGx RFP for clinical labs with testable CPIC or FDA criteria, CLIA/CAP evidence, FHIR payloads, scoring gates, and pilot acceptance tests.
LIMS Integration for PGx Labs: Why PDFs Fail at Decision Support
Connect LIMS and PGx platforms with HL7v2 LRI, FHIR, LOINC, and middleware. Map phenotypes early; validate structured results for clinical decision support.
Branded PGx Reports Put Lab Data in EHR Workflows, Not Just PDFs
See how labs can deploy branded PGx reports with discrete FHIR data, visible evidence grading, living reanalysis, workflow integration, and validation.
Pharmacogenomics in EHRs: Map One Gene Drug Pair in FHIR First
Map pharmacogenomic results to FHIR, store discrete EHR data, build tiered CDS alerts, and set governance before scaling beyond one gene drug pair.