EUA Approval From FDA For Rapid COVID-19 Tests

EUA Approval From FDA For Rapid COVID-19 Tests

Started
June 12, 2020
Signatures: 3,344Next Goal: 5,000
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Why this petition matters

Started by David Kim

COVID-19 has already claimed over 100,000 American lives, and as a Second Wave approaches, we’re not out of the woods yet. 


One of the biggest difficulties that we face is testing that is not only available to the masses, but also fast and accurate. Researchers say that anywhere between 25 and 80 percent of people who have contracted the virus are asymptomatic and unaware that they could possibly be contagious, leading to large groups of men and women who could be spreading COVID-19 without even knowing they’re doing so. 


As we’ve seen over the last few months, COVID-19 has not only claimed thousands of American lives, it’s also gutted countless small businesses across the country and infringed on many of our freedoms that we had previously taken for granted. Until the full extent of this virus’ reach is known, we won’t truly know how to defeat it. Luckily, there is hope that we can get the tests needed to see the full scope of its reach, get our country back to full speed, and do so in a safe and effective manner.


Unlike some of the tests that the United States has already purchased from China that have a less than 50% accuracy rate, there are tests made by leading South Korean biotech companies that are proven to work in the range of 95%. Two of these S. Korean biotech companies, BodiTech Med and DxGen Corp, have produced three rapid-result tests that have proven themselves to be extremely accurate and producible in mass quantities. Unfortunately, these tests are hung up due to government bureaucracy and have yet to be given their proper Emergency Use Authorization (EUA) approval by the Food and Drug Administration (FDA) in spite of approval in 90+ other countries. 


With the ability to produce over 25 million tests a month, it won’t be long before we can get one to every person in the country who needs it. Sign below and help us do our part to restoring the health and freedoms that every person in the United States of America deserves. 


We are petitioning to have the EUA Approvals completed by the FDA for the three tests below...


EUA 201322 - BodiTech Med iChroma COVID-19 Ab Test with iChroma II Analyzer


EUA 201294 - BodiTech Med AFIAS COVID-19 Ab (with AFIAS-1 and AFIAS-6 analyzers)


EUA 201290 - DxGen Epithod 616 COVID-19 IgM/IdG

 

**For additional information or purchasing inquiries, please contact David Kim at david@bluestoneholding.com**

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Signatures: 3,344Next Goal: 5,000
Support now
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