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Originally Posted by
dawg80
I'm not sure why I continue to waste my time with you...wait! yes I do, it's fun!
Bureaucrats run the government. They do everything. I know, I used to work for the government. Quick example, when Hurricane Katrina was bearing down on New Orleans my organization had already made arrangements, plans, and had taken all necessary steps to provide services. Three days later then prez, George W. Bush, declared a national disaster. We had been providing services for better than 24 hrs by then. Point is, we knew our jobs and didn't wait for anyone.
If Covid-19 is running amuck it's not Trump's fault. Those who KNEW they were gonna be on the frontlines dropped the ball. You will keep on blaming Trump because of your bad case of TDS. But, it doesn't change the real truth. Which by the way = the facts. Unlike your boy Biden who says he wants the "truth" not "the facts." :icon_roll:
How does Katrina apply to the current situation? You obviously didn’t read the article from Science that I posted so, I will direct you to one of the key parts:
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In principle, many hospital and academic labs around the country have the capability to carry out tests themselves. The PCR reaction uses so-called primers, short stretches of DNA, to find viral sequences. The CDC website posts the primers used in its test, and WHO publicly catalogs other primers and protocols, too. Well-equipped state or local labs can use these—or come up with their own—to produce what are known as a “laboratory-developed tests” for in-house use.
But at the moment, they’re not allowed to do that without FDA approval. When the United States declared the outbreak a public health emergency on 31 January, a bureaucratic process kicked in that requires FDA’s “emergency use approval” for any tests. “The declaration of a public health emergency did exactly what it shouldn’t have. It limited the diagnostic capacity of this country,” Mina says. “It’s insane.”
On 24 February, APHL asked FDA Commissioner Stephen Hahn for “enforcement discretion” to sidestep the emergency process and allow APHL members labs to use their own tests. On 26 February, Hahn replied that the CDC test could be modified to use just the primers that specifically detect SARS-CoV-2, essentially ignoring the faulty portion of the kits. FDA, in other words, would look the other way to make more widespread testing possible.
So this begs, the question, does Trump and his appointees not understand how things work? Where I am from, that is known as “incompetence.”