How PGxAlly Simplifies the PGx Testing Workflow for Providers
- Shawn Bjorndal
- Oct 14
- 3 min read
In an era where healthcare teams are juggling endless demands, from patient load to documentation, finding ways to simplify care delivery without sacrificing quality is crucial. Pharmacogenomic (PGx) testing offers tremendous potential for improving patient outcomes, but too often, implementation has been bogged down by complex workflows, disconnected systems, and unclear responsibilities.
At PGxAlly, we’ve solved that problem. Our technology was designed from the ground up to make precision medicine simple, integrated, and actionable for healthcare providers.
The Challenge: PGx Testing Has Traditionally Been Cumbersome
For many providers, incorporating PGx testing into daily workflows has felt like adding one more task to an already full plate. Common challenges include:
Manual ordering that requires extra logins or paperwork
Fragmented communication between labs, providers, and patients
Long turnaround times for results, with unclear next steps
Limited interpretation support, leaving clinicians unsure how to act on data
These barriers slow down care and prevent patients from benefiting from precision medicine in a timely way.

The PGxAlly Solution: Seamless Integration, Smarter Workflow
PGxAlly’s platform removes the friction from every step of the process. Our goal is to empower providers to deliver personalized care with the same ease as ordering a routine lab test.
Here’s how our workflow makes it happen:
1. Simple Ordering
Providers can order a PGx test in just a few clicks, directly within their existing workflow. No complex forms, no redundant data entry.
2. Automated Tracking and Notifications
Once a test is ordered, both provider and patient receive updates at each stage. Our system automates communication, keeping everyone informed without additional administrative effort.
3. Fast Turnaround and Results Integration
When results are ready, they are delivered directly into the provider’s workflow, easily integrated into the patient’s chart for easy access. No more hunting through portals or emails.
4. Pharmacist-Led Interpretation
Our clinical pharmacists review and interpret each report, ensuring providers receive clear, actionable recommendations tailored to the patient’s medication profile and genetic insights.
5. Collaborative Follow-Up
PGxAlly’s team helps facilitate next steps, from patient consults to medication adjustments, ensuring that insights translate into action, not just information.

Why Workflow Matters: Faster, Smarter Decisions
Every delay in getting the right medication to a patient can impact adherence, outcomes, and overall satisfaction. PGxAlly eliminates these delays by making pharmacogenomic data immediately usable, within the provider’s natural workflow.
Providers report benefits such as:
Improved medication matching and fewer adverse reactions
Reduced time to therapeutic success
Streamlined documentation and reporting
Greater confidence in precision-based prescribing

Designed for Real-World Clinical Practice
Whether you’re in a large health system, a specialty clinic, or a community pharmacy, PGxAlly’s platform adapts to your environment. Our technology integrates seamlessly with existing systems, including EHRs and pharmacy management tools, making adoption straightforward and scalable.
Most importantly, our pharmacist-led model means you’re never navigating precision medicine alone, you have a partner who understands the science and the clinical reality.
Ready to Simplify Precision Medicine?
At PGxAlly, we believe precision medicine should enhance, not complicate, clinical practice. Our technology allows providers to order, interpret, and act on PGx results seamlessly, transforming what was once a cumbersome process into a smooth, integrated part of patient care.
Learn how PGxAlly can help your practice streamline pharmacogenomic testing and improve patient outcomes.




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