AccessDX
AccessDx Laboratory is dedicated to providing clinical insights that improve patient outcomes through advanced laboratory diagnostics solutions, including COVID-19 testing, pharmacogenomic testing, cancer genomic testing, and infectious disease testing. The company is CLIA-certified, CAP-accredited, and NYSDOH-approved, serving thousands of healthcare providers nationwide with a commitment to clinical excellence, innovation, and health equity.
Industries
Nr. of Employees
large (251-1000)
Products
PGx targeted gene panel
A clinically selected panel of genes and variants to assess medication-related genetic risk across therapeutic areas with clinician-facing interpretive reports.
UTI diagnostic panel (molecular + culture + AST)
Combined molecular detection of common UTI pathogens and resistance markers with culture-based antibiotic sensitivity to support rapid and confirmatory clinical decisions.
Population health and medication risk management platform
Platform functionality for real-time medication monitoring, alerts, cohort analytics, and program analytics to support medication-safety initiatives at facility and network scale.
AccessDx PGx Profile
A pharmacogenomic test profile designed to help healthcare providers identify the safest, most effective medications and dosages based on a patient's unique genetics.
PGx Profile – Comprehensive Panel
Comprehensive pharmacogenomic test panel analyzing an extensive set of genes including ABCB1, ABCG2, ACYP2, ADRA2A, ANKK1, CEP72, COMT, CYP1A2, CYP2B6, CYP2C, CYP2C19, CYP2C8, CYP2C9, CYP2D6, CYP3A4, CYP3A5, CYP4F2, DPYD, DRD2, F2, F5, FKBP5, G6PD, GRIK4, HCP5/HLA-B*57:01, HTR2A, HTR2C, IFNL4, MTHFR, NUDT15, OPRM1, SLC6A4, SLCO1B1, TPMT, UGT1A1, UGT2B15, and VKORC1.
Pharmacogenomics
Comprehensive pharmacogenomic panel offered by AccessDx Laboratory to test how genes affect medication response.
PGx targeted gene panel
A clinically selected panel of genes and variants to assess medication-related genetic risk across therapeutic areas with clinician-facing interpretive reports.
UTI diagnostic panel (molecular + culture + AST)
Combined molecular detection of common UTI pathogens and resistance markers with culture-based antibiotic sensitivity to support rapid and confirmatory clinical decisions.
Population health and medication risk management platform
Platform functionality for real-time medication monitoring, alerts, cohort analytics, and program analytics to support medication-safety initiatives at facility and network scale.
AccessDx PGx Profile
A pharmacogenomic test profile designed to help healthcare providers identify the safest, most effective medications and dosages based on a patient's unique genetics.
PGx Profile – Comprehensive Panel
Comprehensive pharmacogenomic test panel analyzing an extensive set of genes including ABCB1, ABCG2, ACYP2, ADRA2A, ANKK1, CEP72, COMT, CYP1A2, CYP2B6, CYP2C, CYP2C19, CYP2C8, CYP2C9, CYP2D6, CYP3A4, CYP3A5, CYP4F2, DPYD, DRD2, F2, F5, FKBP5, G6PD, GRIK4, HCP5/HLA-B*57:01, HTR2A, HTR2C, IFNL4, MTHFR, NUDT15, OPRM1, SLC6A4, SLCO1B1, TPMT, UGT1A1, UGT2B15, and VKORC1.
Pharmacogenomics
Comprehensive pharmacogenomic panel offered by AccessDx Laboratory to test how genes affect medication response.
Services
Targeted PGx panel testing with clinical interpretation to identify drug-gene interactions and support medication optimization.
PCR-based pathogen detection and reporting for infectious disease diagnosis and stewardship initiatives.
Service combining rapid molecular detection of urinary pathogens and resistance markers with culture and AST to enable faster and confirmatory clinical decisions.
Continuous drug-gene monitoring and pharmacogenomic risk alerts delivered into clinical workflows and EHRs to help identify and remediate medication risks.
Investigational variant-detection services using sequencing to identify emergent pathogen variants from PCR-positive samples, offered as a surveillance capability.
Targeted PGx panel testing with clinical interpretation to identify drug-gene interactions and support medication optimization.
PCR-based pathogen detection and reporting for infectious disease diagnosis and stewardship initiatives.
Service combining rapid molecular detection of urinary pathogens and resistance markers with culture and AST to enable faster and confirmatory clinical decisions.
Continuous drug-gene monitoring and pharmacogenomic risk alerts delivered into clinical workflows and EHRs to help identify and remediate medication risks.
Investigational variant-detection services using sequencing to identify emergent pathogen variants from PCR-positive samples, offered as a surveillance capability.
Expertise Areas
- Pharmacogenomics
- Molecular infectious disease diagnostics
- Hereditary cancer genomics
- Clinical decision support and EHR integration
Key Technologies
- Polymerase chain reaction (PCR)
- Next-generation sequencing (NGS)
- Microbiology culture and antibiotic susceptibility testing (AST)
- Bioinformatics for clinical reporting
News & Updates
Partnership to enhance diagnostic solutions.
A session on personalized medication management.
Seamless integration to improve resident care.
Pharmacogenomic Testing as a Preventive Approach to Tardive Dyskinesia Risk Reduction and Management
Exploring the benefits of pharmacogenomics testing.
A tutorial on CYP2D6 structural variation testing.
Recognizing her contributions to genetics and genomics.
Partnership to enhance diagnostic solutions.
A session on personalized medication management.
Seamless integration to improve resident care.
Pharmacogenomic Testing as a Preventive Approach to Tardive Dyskinesia Risk Reduction and Management
Exploring the benefits of pharmacogenomics testing.
A tutorial on CYP2D6 structural variation testing.
Recognizing her contributions to genetics and genomics.