Trusted by 15+ major health systems

Personalized medicine, powered by genetics

ActX integrates pharmacogenomics directly into your EHR, enabling real-time genetic insights that improve patient outcomes and eliminate guesswork in prescribing.

Integrated with leading EHR systems

EpicOracle HealthathenahealthNextGen

Patient: Jane Doe

DOB: 03/15/1985

Genetic Profile Active
!
Pharmacogenomic Alert

CYP2C19 Poor Metabolizer detected. Consider alternative to Clopidogrel.

CYP2D6

Normal Metabolizer

SLCO1B1

Decreased Function

98%

Alert Accuracy

2.3s

Avg Response Time

15M+

Patients served

Genetic insights delivered across partner networks

500+

Medications covered

FDA-approved drugs with pharmacogenomic data

40%

Reduction in ADRs

Adverse drug reactions prevented through genetic screening

<3 sec

Real-time alerts

Instant genetic guidance during prescribing workflow

Solutions

Precision medicine for every stakeholder

Whether you're a health system, provider, practice, or individual, ActX makes genomic medicine accessible and actionable.

Health Plans & ACOs

Reduce medication-related costs, improve STAR ratings, and drive better outcomes across your member population.

  • Risk Stratification
  • Cost Reduction Analytics
  • Quality Metric Improvement

Health Systems

Deploy EHR-integrated genomic decision support across your entire network. Go live in weeks, not months.

  • Epic & Oracle Health Integration
  • Customizable Alerts
  • Enterprise Analytics

Providers

Add precision medicine to your practice without disrupting workflow. Real-time pharmacogenomics at the point of care.

  • Seamless EHR Workflow
  • Drug-Gene Interactions
  • Clinical Recommendations

Practices

Differentiate your practice with cutting-edge genetic services. Improve outcomes and patient satisfaction.

  • Quick Implementation
  • Patient Engagement Tools
  • Competitive Advantage

Individuals

Leverage your DNA to help your doctor make better decisions. Compatible with 23andMe and other consumer tests.

  • 23andMe Integration
  • Medical-Grade Analysis
  • Secure Data Sharing
For Health Plans & ACOs

Transform population health with precision pharmacogenomics

Adverse drug reactions cost the U.S. healthcare system over $528 billion annually. ActX helps health plans and ACOs identify at-risk members before costly events occur, driving measurable improvements in outcomes and total cost of care.

Platform Capabilities

  • Population-level pharmacogenomic risk stratification
  • Integration with claims data for targeted outreach
  • Member engagement programs with personalized insights
  • Provider network education and adoption support
  • Real-time alerts for high-risk prescription patterns
  • Comprehensive reporting for quality measurement
$1,200+
Saved per member annually

Reduce adverse drug events, hospitalizations, and medication waste through precision prescribing.

40%
Fewer ADR-related admissions

Proactively identify high-risk members before costly adverse events occur.

15-20%
Improvement in STAR ratings

Drive quality metrics with better medication adherence and outcomes.

3.2x
ROI within 12 months

Documented return on investment from reduced medical costs and improved quality scores.

How Health Plans Use ActX

Member Stratification

Identify members with genetic variants that increase risk for adverse drug reactions across common medication classes like statins, blood thinners, and pain medications.

Targeted Interventions

Trigger care management outreach when high-risk members are prescribed medications that may cause adverse events based on their genetic profile.

Quality Improvement

Improve medication adherence and HEDIS measures through personalized insights that help members understand why certain medications work better for them.

"ActX helped us identify over 12,000 members at high risk for statin-related myopathy. By proactively adjusting their care plans, we avoided an estimated $8.4 million in adverse event costs in the first year alone."
JM
Dr. Jennifer Martinez
Chief Medical Officer, Regional Health Plan

How It Works

From genetics to actionable insights in seconds

ActX bridges the gap between genetic data and clinical decision-making, delivering precision medicine at the speed of care.

01

Genetic Testing

Patient completes a simple genetic test through your organization or uploads existing results from 23andMe or clinical labs.

02

EHR Integration

ActX securely processes genetic data and integrates the patient's pharmacogenomic profile directly into your EHR system.

03

Real-Time Alerts

During prescribing, clinicians receive instant alerts about drug-gene interactions, dosing recommendations, and alternatives.

04

Better Outcomes

Patients receive medications optimized for their genetic profile, reducing adverse reactions and improving therapeutic efficacy.

Trusted Nationwide

Leading health systems choose ActX

From academic medical centers to community hospitals, organizations trust ActX to deliver genomic decision support at scale.

Yale New Haven Health
Mount Sinai
NorthShore
Baptist Health
Nemours Children's
Cone Health
UAB Medicine
Lakeland Regional
Vancouver Clinic
Nicklaus Children's
"ActX has transformed how we approach prescribing. The seamless EHR integration means our clinicians get genetic insights exactly when they need them, without any extra clicks or disruption to their workflow."

Dr. Sarah Chen

Chief Medical Officer, Regional Health System

EHR Integrations

Built into the systems you already use

ActX integrates natively with all major EHR platforms, ensuring genetic insights appear exactly where clinicians need them—within their existing workflow.

10+EHR Platforms
2wkTypical Go-Live
0Workflow Disruption
EpicEHR
Oracle HealthEHR
athenahealthEHR
NextGenEHR
VeradigmEHR
eClinicalWorksEHR
Greenway HealthEHR
CGMEHR
NewCropPrescribing
AprimaEHR

Ready to bring precision medicine to your organization?

Join leading health systems nationwide in delivering personalized care powered by genetics. Schedule a demo to see ActX in action.