Revolutionize patient care with myPGx
Our pharmacogenomics solution, myPGx, enables providers to tailor treatment by identifying drug-gene interactions for 100+ medications. Minimize costly trial and error and maximize efficacy by leveraging the power of genomics.
Covering 100+ drugs representing ∼1 billion prescriptions annually⁶ across 3 categories
Pain Management
Leverage precision medicine for a safer way to address patient pain management.
Cardiovascular Health
Identify how genetic variability can affect patient cardiovascular drug response and related outcomes.
Behavioral Health
Personalize medication selection and dosage for individuals with conditions like depression, anxiety, or ADHD.
Drive goals forward with myPGx
Heighten patient experience
myPGx can help providers get patients to the right medication faster, boosting adherence to treatment and confidence in health plans.
Reduce costs
Unsuitable treatment brings needless strain to healthcare systems. Reduce emergency room visits, hospital admissions, and physician appointments by guiding optimal medication from the start.
Improve outcomes
Improve patient outcomes and adherence to prescriptions with precision medicine, for less adverse side effects and trial and error, and more therapeutic benefit.
Annual cost of non-optimized prescription drug therapy¹
Of patients don't find relief until the 4th medication²
Deaths caused by adverse drug reactions per year³
Emergency department visits each year due to adverse drug events⁴
myPGx covers these key genes
Among the 25 gene panel covering 3 primary categories, are drugs for treatments for oncology and HIV, as well as conditions such as GERD.
Our comprehensive gene panel is designed to address the most commonly prescribed medication in the United States.
Design your solution
Get in touch with us so we can work together to build a solution for your needs
An end-to-end care solution
Direct delivery of sample collection kits
Medical support at your fingertips
High-complexity CLIA and CAP lab
Physician reviewed results in 7-10 days
Patient and PCP support with results
100% encrypted
How does this solution work
Our accessible healthcare solutions are customized to meet your specific goals, and each step of the process can be adapted to best suit your population.
Multi-channel engagement and education
We offer custom-built announcement and engagement strategies to maximize compliance, from fully digital packages to device-free communication. Our Genetics Knowledge Hub was created by experts to guide your people through the basics of genetics and what they'll learn from their results.
Simple saliva sample collection from home
We meet your people where they are with kits delivered directly to their homes. Your people will feel empowered with our easy-to-use sample collection kits, no matter what their experience or digital fluency is. We offer both printed and digital instructions depending on their needs.
Downloadable result report for easy sharing
Our wholly-owned solution ensures a streamlined delivery of lab results directly to a secure online account. Patients can easily share these results so their provider can make informed decisions about their healthcare to minimize adverse effects and make the right decisions faster.
Dynamic clinical support for providers and patients
Our affiliate pharmacy team is available to help walk patients through their result report, next steps, and how to share their report with their provider.
Our peer-to-peer clinical support guides providers in integrating myPGx findings into patient care to inform optimal treatment.
Better treatment for life
myPGx results, based on unchanging genetic sequences, help inform lifelong medication decisions. One saliva sample allows patients and healthcare providers to collaborate for precise prescriptions, maximizing therapeutic benefits.
myPGx report
Patients and providers can work together with an easily downloadable report to better inform their healthcare
Learn more about myPGx
Get in touch at b2bsolutions@letsgetchecked.com
Developed by genetic and clinical experts
We work with trusted experts to build experiences, so your population can get the answers they need.
Dr. Avni Santani
Chief Genomics Officer
Dr. Robert Mordkin, MD
Chief Medical Officer
Dr. Kate Karfilis
Director of Product - Genomics
Wendi Gill
Genetic Counselor
Bronwyn Ramey
Director of Precision Medicine
Kristin O'Connor
Nurse Manager
Request a demo
Get in touch with us so we can design your solution
1. NLM: Cost of Prescription Drug-Related Morbidity and Mortality
2. Sharon Liao WebMD: Medication Strategies for Treatment-Resistant Depression
3. FDA: Preventable Adverse Drug Reactions: A Focus on Drug Interactions
4. CDC: Adverse Drug Events in Adults
5. NIH: Projected Prevalence of Actionable Pharmacogenetic Variants and Level A Drugs Prescribed Among US Veterans Health Administration Pharmacy Users
6. FDA Table of Pharmacogenetic Associations