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  • COVID-19: Endemic Disease
  • Products
    • ASSURE-100 Home Tests
    • ASSURE-100 POC Tests
    • Buy ASSURE-100 Tests
  • News & Updates
  • Contact Us
  • BUY TESTS
Does the CDC Still Provide COVID-19 Quarantine Guidance in 2025?

Does the CDC Still Provide COVID-19 Quarantine Guidance in 2025?

by Oceanit | Mar 7, 2025 | Education, General, Government

Does the CDC Still Provide COVID-19 Quarantine Guidance in 2025? With COVID-19 transitioning into an endemic phase, public health policies continue to evolve. As of March 2025, there have been significant changes to federal guidance regarding quarantine, isolation,...
Matthew Memoli Named Acting NIH Head: Insights on COVID

Matthew Memoli Named Acting NIH Head: Insights on COVID

by Oceanit | Jan 24, 2025 | General, Government, National News

Matthew Memoli Named Acting NIH Head: Insights on COVID In a pivotal move for U.S. public health leadership, Dr. Matthew Memoli has been named acting director of the National Institutes of Health (NIH). Known for his expertise in infectious diseases and his nuanced...
NIH RECOVER Initiative: Advancing Research for Long COVID Solutions

NIH RECOVER Initiative: Advancing Research for Long COVID Solutions

by Oceanit | Dec 27, 2024 | General, Government, National News

NIH RECOVER Initiative: Advancing Research for Long COVID Solutions The NIH’s Ongoing Efforts in the Researching COVID to Enhance Recovery (RECOVER) Initiative: What It Is and How It Helps with Long COVID The COVID-19 pandemic has reshaped the landscape of global...

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Copyright 2025 Oceanit Foundry LLC. The ASSURE-100 Rapid COVID-19 Test has not been FDA cleared or approved, but has been authorized by FDA under an EUA. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb- 3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
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