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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
Strategies for Students Recovering Lost Educational Time Post-Pandemic in 2025

Strategies for Students Recovering Lost Educational Time Post-Pandemic in 2025

by Oceanit | Feb 12, 2025 | Education, Future

Strategies for Students Recovering Lost Educational Time Post-Pandemic in 2025 The COVID-19 pandemic led to significant disruptions in education, resulting in notable learning losses for students across the United States. As of 2025, various strategies have been...
COVID-19 Recovery Period for New Variants in 2025: What to Expect

COVID-19 Recovery Period for New Variants in 2025: What to Expect

by Oceanit | Jan 31, 2025 | Education, National News

COVID-19 Recovery Period for New Variants in 2025: What to Expect With ongoing seasonal surges, Rapid Home Tests are a vital tool for staying healthy and protecting your family and loved ones in 2025. Experts say that we should stock our home medicine cabinets this...
COVID-19 Impact: Hardest Hit Countries and Those Still Struggling in 2025

COVID-19 Impact: Hardest Hit Countries and Those Still Struggling in 2025

by Oceanit | Dec 12, 2024 | Future, Government, International News

COVID-19 Impact: Hardest Hit Countries and Those Still Struggling in 2025 Global Impact of COVID-19: Countries Hardest Hit and Those Still Struggling in 2025 The COVID-19 pandemic has left a profound impact on nations worldwide, with some countries experiencing...

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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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