Houston Concierge Medicine Partners With Cardio Diagnostics to Offer the Epi+Gen CHD Test in Their Executive Health Program
Cardio Diagnostics Holdings Inc (Nasdaq: CDIO) has partnered with Houston Concierge Medicine to offer the Epi+Gen CHD precision cardiovascular disease test, targeting executives in Houston, Texas. This test utilizes epigenetics and AI to identify coronary heart disease risks, enhancing preventive care for high-stress professionals. The collaboration highlights a growing trend of executive physicals aimed at long-term health benefits, potentially reducing future medical costs and absenteeism. The Houston practice emphasizes its commitment to best-in-class diagnostic solutions, addressing heart health concerns among its clientele.
- Partnership with Houston Concierge Medicine expands market reach for Epi+Gen CHD test.
- Utilization of advanced technologies (epigenetics and AI) in the test enhances precision in identifying heart disease risks.
- Growing trend of executive physicals may enhance preventive care and reduce future healthcare costs.
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Leading concierge medicine practice in
Executive physicals are becoming more common as employers recognize the long-term value of preventive care and wellness for their executives. Executive physicals are important employee benefits because they provide employers with the opportunity to promote health and wellness among key employees. They can help identify and address potential health risks before they become serious, reducing medical costs and absenteeism over time.
“We are excited to partner with
“At Houston Concierge Medicine, we’re committed to providing our patients with best-in-class diagnostic solutions. And since heart disease is top of mind for so many of our clients who work in fast-paced, stressful environments, the addition of Epi+Gen CHD will enable our practice to provide patients with objective and non-invasive tests to determine their risk for heart disease. We’re proud to partner with
About Houston Concierge Medicine
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This press release includes "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Words such as "expect," "estimate," "project," "budget," "forecast," "anticipate," "intend," "plan," "may," "will," "should," "believe," and similar expressions are intended to identify such forward-looking statements. Forward-looking statements include, without limitation, the Company’s expectations with respect to future performance, development and commercialization of products and services, the potential benefits and impact of the Company’s products and services, potential regulatory approvals, and the size and potential growth of current or future markets for the Company’s products and services. Forward-looking statements are statements about future events that are based on current expectations and assumptions and, as a result, are subject to risks and uncertainties that could cause the actual results to differ materially from the expected results. These statements are based on various assumptions, whether or not identified in this press release, and are not intended to serve as, and they must not be relied on by an investor as, a guarantee, an assurance, a prediction or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and will differ from assumptions. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that Epi+Gen CHD™, Cardio’s initial test, is accepted and adopted by patients, healthcare professionals and participants in other key channels; the impact of COVID-19 on the Company’s business; the inability to maintain the listing of the Company’s common stock on Nasdaq; changes in applicable laws or regulations; the inability of the Company to raise financing in the future; the inability of the Company to obtain and maintain regulatory clearance or approval for its tests, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that could serve the same or similar functions as the Company’s products and services; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical tests conducted using the Company’s products and services; the Company’s estimates regarding expenses, future revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the
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