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Our partners

We work with leading genomics and healthcare organizations to bring advanced testing to the patients and providers we serve.

Technology partner

Oncology NGS

Panel and technology partner

Celemics

Visit celemics.com

Celemics is a genomics company founded in 2010 and headquartered in Seoul, Korea, with a U.S. office in California. Celemics designs the hybrid-capture panels and target-enrichment chemistry behind our oncology NGS portfolio, and AchieveDx runs the testing and reporting. Our PGx testing is separate and is not a Celemics product.

  • Proprietary probe-synthesis technology for hybrid-capture target enrichment
  • More than 10 years designing and customizing NGS panels
  • ctDNA panels developed with Seoul National University Hospital since 2017
  • Publicly listed genomics company (KOSDAQ)
Panels with AchieveDxOncoRiskCancerScreen 50ctDNA ColorectalctDNA BreastctDNA Lung
Partner with AchieveDx

Interested in working with us?

We partner with diagnostics companies, health systems and organizations that share our focus on making genomic testing accessible and actionable.

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Build your testing program

Partner with AchieveDx.

Three quick steps. A program specialist follows up with a recommended workflow, materials and a go-live timeline.

Your program so farNothing yet

Your organization and the tests you pick will show here.

Prefer to talk now?
(618) 224-4383
info@achievedx.com
Step 1 of 3Your organization

What kind of organization are you?

STEP 1We review your request

A specialist reads your answers before reaching out.

STEP 2A short discovery call

We learn your workflow, patient population and goals.

STEP 3Your program plan

Recommended workflow, kits and materials, and a go-live timeline.

Questions

Frequently asked

What is pharmacogenomic (PGx) testing?

A PGx test reads genes that control how your body activates and clears medications. Providers use the results to choose drugs and doses that are more likely to work and less likely to cause side effects.

How is the sample collected?

With a simple cheek swab. No needles or blood draw. It can be done in a pharmacy, physician office, hospital unit or at a resident's bedside.

How long do results take?

Typically 5–7 days after the lab receives the specimen. SNF programs receive results by encrypted email or fax within 5–10 business days.

Is it covered by insurance?

Medicare covers PGx testing when a clinician is considering or using a specific drug with an actionable gene-drug interaction and needs the result for that decision. Medicaid and commercial coverage vary by state and plan. We verify coverage first and confirm any cost with the patient in advance.

Does the test need to be repeated?

No. Your genes don't change, so one test can guide medication decisions for life.