ActX
Genomic Decision Support. In your workflow.
Overview
ActX is a genomic clinical decision support service that integrates directly into a provider's existing EHR. Once a patient's genetic data is in the system, ActX works in the background, alerting the physician in real-time if they are prescribing a medication that could be ineffective or cause an adverse reaction based on the patient's genetics. The service covers pharmacogenomics, carrier status, and hereditary risks.
✨ Key Features
- Real-time alerts within the EHR prescribing workflow
- Covers pharmacogenomics (PGx)
- Checks for actionable hereditary risks (e.g., cancer, cardiovascular)
- Provides carrier status information
- Patient-friendly genomic profiles
- Integrates with major EHRs
🎯 Key Differentiators
- Broad scope beyond PGx, including actionable hereditary risks and carrier status.
- Real-time, interruptive alerts are deeply embedded in the prescribing workflow.
- Service model includes both the testing and the ongoing decision support.
Unique Value: Makes genomic insights immediately actionable and unavoidable for the clinician by integrating live alerts directly into the EHR prescribing workflow, covering more than just pharmacogenomics.
🎯 Use Cases (4)
✅ Best For
- EHR-integrated pharmacogenomic alerting
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Complex genomic data analysis for research
- Somatic variant interpretation for oncology
🏆 Alternatives
Unlike platforms that exist outside the EHR or require manual look-up, ActX provides automated, real-time checks at the moment of decision-making.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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