Is That COVID-19 Test FDA Approved?

Aug 12, 2020

Is That COVID-19 Test FDA Approved? Testing Misnomers and Related Issues

The most frequently asked question of them all when we get a call inquiring about the Coronavirus testing services we offer is, “Is it FDA approved?”
The short answer is, no it’s not FDA approved and neither are any of the tests available anywhere. In fact there is no such thing as an FDA Approved test yet because FDA approval takes years and requires exhaustive data aggregation and validation. It’s a process for which we sometimes have not enough time because of a pressing need.
So what’s the deal with FDA “approved” tests we hear about in ads and in the media?
The FDA has a tool or option for allowing medical treatments, tests and devices to come to market prior to their being “approved”. It’s called an Emergency Use Authorization (EUA) and it’s what the FDA is granting to companies meeting a certain low-bar criteria so tests that would take months or years to validate (and many test that would never achieve validation because they don’t work) are available right now.
The EUA though can be misleading and has caused myriad issues, including allowing thousands of inaccurate and unreliable tests to flood into the country from China, Korea and Russia.
The time consuming rigors of gaining FDA Approval exists to protect against these same issues. The EUA therefore goes against the very mandate of the FDA and its processes.
The FDA’ description of their EUA tool is as follows:
“During a public health emergency, the FDA can use its Emergency Use Authorization (EUA) authority to allow the use of unapproved medical products, or unapproved uses of approved medical products, to diagnose, treat, or prevent serious or life-threatening diseases when certain criteria are met, including that there are no adequate, approved, and available alternatives.”
To be granted and EUA requires no real validation and no FDA review of the COVID-19 tests being sold or the dozens of companies making and or selling the tests. To put it plainly, no one tests the tests independently of the company that makes them.
A test with an FDA EUA therefore does not have to be proven accurate, reliable or even inspected to ensure sanitary packaging or that it meets standards for importation.
Think of the EUA like a tin badge given by an Old West Sheriff to members of his quickly formed posse, chosen only because they have a good horse and a rifle. Having been “deputized” does not indicate quality at all but an emergency need for something in place of nothing at all.

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