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Together, we can:
Optimize and automate workflows that support clinicians and staff
Address population health, equity, and quality goals
Provide personalized, end-to-end support for patients along their journey
Real-world experience
Cancer screening solutions that work on your terms to optimize cancer detection
Our screening portfolio is designed to get every eligible patient screened with the right test. We're focused on providing innovative solutions at speed and scale, in one comprehensive portfolio, backed by end-to-end support. Our cancer screening portfolio includes:
Colorectal cancer (CRC) screening
- For average-risk patients aged 45+ — the Cologuard Plus® test is an FDA-approved stool DNA test that offers early-stage detection of colorectal cancer (CRC).
1 - For patients who remain unscreened — the SimpleScreen™ CRC test is an FDA approved screening option for average-risk patients 45+. CRC blood tests are recommended by the American Cancer Society (ACS) for those who will not complete a preferred screening test.
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Multi-cancer early detection
- The Cancerguard® test — an innovative multi-cancer early detection (MCED) test that complements standard-of-care screening and can help detect multiple cancers with a simple blood draw.
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Precision oncology: Testing for every stage of care
Exact Sciences’ Precision Oncology portfolio doesn't stop with a test's science. It also reflects the realities of the clinical setting and what providers can face when ordering tests and delivering results to patients.
Pairing comprehensive, world-class genomic tests like the Oncotype DX® test with a connected digital infrastructure
- Helps to efficiently create a complete picture of each patient's unique cancer
- Enables providers and their patients to focus on what matters most—the best way forward
We’re equipped to integrate solutions into your workflows, streamlining your genomic cancer testing and helping you match your patients with emerging personalized treatments.
ExactNexus™ technology platform: Streamlined and secure care
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Footnotes and references
Important Information about the Cologuard products
The Cologuard test and Cologuard Plus test are indicated to screen adults, 45 years or older, who are at average risk for CRC. A positive result may indicate the presence of colorectal cancer (CRC) or advanced precancerous lesions (APL) and should be followed by a colonoscopy. Not a replacement for colonoscopy in high-risk individuals. False positive and negative results may occur. Rx only. See more information about Cologuard and SimpleScreen CRC at Cologuard.com/risk- information.
Important Information about the SimpleScreen CRC test
SimpleScreen CRC is indicated for colorectal cancer screening in adults aged 45 years and older who are at average risk for the disease. Patients with a positive result should be followed by colonoscopy. SimpleScreen CRC is not a replacement for diagnostic colonoscopy or for surveillance colonoscopy in high-risk individuals.
Precaution: Based on data from clinical studies, SimpleScreen CRC has limited detection (57%) of Stage I colorectal cancer (64% when U.S. 2020 Census age-sex adjusted) and does not detect 87% of advanced precancerous lesions (86% when U.S. 2020 Census age-sex adjusted). One out of 10 patients with a negative SimpleScreen CRC result may have a precancer that would have been detected by a screening colonoscopy. Rx only. IVD. See more information about Cologuard and SimpleScreen CRC at Cologuard.com/risk-information.
Developed and manufactured by Freenome, LLC. Distributed by Abbott.
Important Information about the Cancerguard test
The Cancerguard test is indicated for use in adults ages 50-84 with no known cancer diagnosis in the last three years. The test does not detect all cancers and is not a replacement for existing recommended cancer screening or diagnostic modalities for cancer. The test is not indicated for screening of breast and prostate cancer and was not evaluated for the detection of pre-cancerous lesions. False positive and negative results may occur. The Cancerguard test is a Laboratory Developed Test, it has not been cleared or approved by the US Food and Drug Administration. Rx only. See more at cancerguard.com/indications-for-use.