*SNORT* Just Found the MOTHER of All Foreshadowing Pic-Posts from Eric Swalwell and...
YO Cali? They BOTH Suck: Katie Porter Trips SPECTACULARLY During Bizarre Victory Lap...
Catherine Herridge Shares Declassified Doc Drop (Adam Schiff Told HUGE Lies About Trump...
Oh, Honey... WAT? Hack Journo Drops the MOST Pathetic Excuse YET for Not...
Barack Obama and Hillary Clinton Just Made the Left's Definition of 'Democracy' VERY...
Monday Morning Meme Madness
Slant Rant: 'Journalist' Jim Acosta Laments Not Being More Opinionated About Trump on...
Desperate Dems May Call on Kamala Harris in Hopes of Avoiding All-Republican California...
Eric Swalwell Suspends Calif. Gubernatorial Campaign and Now EVERYBODY Has the Same Questi...
Dem Robert Garcia Wants Eric Swalwell to Leave CA Governor’s Race, Silent on...
Report: Artemis II Pilot Makes a Point of Thanking God
Sen. Rick Scott Trumpets Busting the Filibuster
WATCH Mark Warner Squirm As CNN's Dana Bash Asks Him As a Democrat...
Meghan McCain Shuts TDS-Inflicted Barbara Comstock DOWN in BRUTAL Back and Forth About...
In Case Your Skin Hasn't Crawled ENOUGH Already --> Check Out Eric Swalwell's...

There is a way to stop the pandemic by Christmas without a lockdown, if only the FDA bureaucracy would get out of the way, that is

 

Michael Mina, a “MD, PhD, Assistant Professor of Epidemiology and Immunology, Harvard T.H. Chan School of Public Health, Center for Communicable Disease Dynamics and Associate Medical Director of Microbiology, Brigham and Women’s Hospital, Harvard Medical School” has a piece out in Time magazine outlining how we can stop the coronavirus pandemic by Christmas without a lockdown or having to wait for vaccines.

Advertisement

In summary, we need at-home rapid antigen tests that are currently being held up by the FDA bureaucracy. From Time:

The antigen test technology exists and some companies overseas have already produced exactly what would work for this program. However, in the U.S., the FDA hasn’t figured out a way to authorize the at-home rapid antigen tests because the FDA is used to regulating medical devices, not public health screening tools. Thus, every test that is authorized, regardless of whether it is designed for medicine or public health, is authorized as a clinical medical device. Requiring public health tools to meet medical device specifications has caused company after company to delay their FDA submissions in a never ending attempt to meet the FDA’s guidelines—for example the need to separately qualify a rapid antigen test for symptomatic versus asymptomatic use.

And here’s Dr. Mina with a must-read thread on what needs to be done to get these at-home tests in use right now:

Advertisement

Advertisement

Advertisement

Let’s get this done!

***

 

Join the conversation as a VIP Member

Recommended

Trending on Twitchy Videos

Advertisement
Advertisement
Advertisement