Le Lézard
Classified in: Health, Business, Covid-19 virus
Subjects: LIC, CSR

Helix partners with San Diego County to make COVID-19 testing accessible for those who need it most


SAN DIEGO, July 13, 2020 /PRNewswire/ -- Helix, the leading population genomics company, today announced a partnership with San Diego County to make COVID-19 testing accessible across the County to those who need it most. As part of this important public-private partnership, Helix will be providing San Diego County with up to 2,000 COVID-19 tests per day.

"We're incredibly proud to partner with San Diego County to expand access to COVID-19 testing at a time of unprecedented need," said Marc Stapley, Helix President and CEO. "Given our years of experience in collecting and handling biological samples and reporting clinical results at significant scale, we're uniquely qualified to help our community during this public health crisis."

"Communities across the country have been struggling to provide access to fast and reliable COVID-19 testing," said Greg Cox, Chairman of the San Diego County Board of Supervisors. "Through this strategic partnership with Helix, we've made a major step forward in meeting the need for COVID-19 testing here in San Diego."

"It is critical to public health that San Diego have access to reliable and rapid COVID-19 testing," said Nick Macchione, Director of San Diego County's Health and Human Services Agency. "We view Helix as a true partner in our fight against COVID-19."

San Diego County will be using the Helix? COVID-19 Test, a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in upper respiratory nasopharyngeal (NP), anterior nares (AN) and oropharyngeal (OP) swab specimens from individuals suspected of COVID-19 by their healthcare provider. Emergency use authorization is pending and Helix is working interactively with the FDA.

The Helix? COVID-19 Test is part of Helix's broader end-to-end test system, which is available nationally to health systems, employers, governments, and other organizations in need of sensitive, scalable, and fully kitted COVID-19 testing solutions. It includes:

To support further expansion of its testing capabilities and capacity, Helix has also filed an additional EUA for a higher throughput and more sensitive COVID-19 test based on next-generation sequencing technology, which is currently under review by the FDA.

The Helix? COVID-19 test has not been FDA cleared or approved. This test has been validated in accordance with the FDA's Guidance Document (Policy for Diagnostics Testing in Laboratories Certified to Perform High Complexity Testing under CLIA prior to Emergency Use Authorization for Coronavirus Disease-2019 during the Public Health Emergency). FDA independent review of this validation and issuance of Emergency Use Authorization (EUA) is pending.

Additional information, including important test information and limitations, is available at helix.com/COVID. Organizations in need of a COVID-19 testing solution can contact Helix by emailing [email protected].

About Helix

Helix is the leading population genomics company operating at the intersection of clinical care, research, and genomics. Its end-to-end platform enables health systems, life sciences companies, and payers to advance genomic research and accelerate the integration of genomic data into clinical care. Powered by one of the world's largest CLIA / CAP next-generation sequencing labs and its proprietary Exome+® assay, Helix supports all aspects of population genomics including recruitment and engagement, clinically actionable disease screening, return of results, and basic and translational research. In response to the COVID-19 public health crisis, Helix has launched a sensitive and scalable end-to-end COVID-19 test system to meet the needs of health systems, employers, governments, and other organizations across the country. Learn more at www.helix.com

SOURCE Helix


These press releases may also interest you

at 01:20
Biophytis SA (Euronext Growth Paris:ALBPS), ("Biophytis" or the "Company"), a clinical-stage biotechnology company specialized in thedevelopment oftherapeutics for age-related diseases, today annouces that it will change the ratio...

18 avr 2024
The report titled "Clinical Trials Matching Software Market by Functionality (Analytics & Reporting, Compliance Tracking, Data Management), Deployment (Cloud & Web Based, On-Premise), End-Use - Global Forecast 2024-2030" is now available on...

18 avr 2024
South Korea's biotechnology company Hyundai Bioscience (CEO Oh Sang-gi, www.hyundaibioscience.com) announced on April 15 that it would carry out global clinical tests aimed at treating all serotypes of Dengue virus infection....

18 avr 2024
The economic turmoil triggered by the COVID-19 pandemic has led to a sharp decrease in the number of self-employed individuals in the United States, with a 22% reduction...

18 avr 2024
WHY: Rosen Law Firm, a global investor rights law firm, announces the filing of a class action lawsuit on behalf of purchasers of common stock of QuidelOrtho Corporation between February 18, 2022 and April 1, 2024, both dates inclusive (the "Class...

18 avr 2024
Takeda (TSE:4502/NYSE:TAK) today announced that the U.S. Food and Drug Administration (FDA) has approved ENTYVIO® (vedolizumab) subcutaneous (SC) administration for maintenance therapy in adults with moderately to severely active Crohn's disease (CD)...



News published on and distributed by: