ICE SHREDS 'Asinine, Legally Illiterate' Abigail Spanberger for Putting Violent Illegal Ov...
Iranian-American Journo Masiah Alinejad Has a DIRECT MESSAGE Just for Kamala Harris and...
'Secret' Iran Supreme Leader Meeting Destroyed As Rubio Sets the Record Straight
Wait, What?! Bill Clinton Casually Drops YUGE JB Pritzker Epstein Bombshell During His...
What a DICK! Jonathan Turley OWNS Richard Blumenthal With His OWN Words for...
Megyn Kelly Got Operation Epic Fury in Iran DEAD Wrong
Brit Hume HUMILIATES Chuck Todd and Chris Cillizza As Only HE Can for...
SUPER Inconvenient (for Democrats) Obama Video Drops and We Are Here FOR IT...
Iranian Women Celebrating FREEDOM Take Nasty, 'Antisemitic Karen' Slut-Shaming Them As HOO...
Eric Swalwell Tries Picking a Fight With Dave Portnoy Over Operation Epic Fury...
Jihadis NEVER Learn: Israel Takes Out Gathering of Islamic Experts Meeting to Select...
WOW: Abigail Spanberger's Admin and VA Democrats ALREADY Have EMBARRASSING Yet DELISH Scan...
Scott Jennings Renders Anti-Trump CNN Panel SPEECHLESS With Straight-Fire Defense of Iran...
Democrat Podcaster Jim Acosta Fears That Republican Scott Jennings Will Soon Have His...
Mark Cuban: Democrat Party Should Shell Out Millions to Hire Mamdani’s Socialist Social...

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