No. You presented questions and claimed they were legal. They were not phrased in legal terminology. They did not quote apposite law. They did not refer to legal judgements. In short, you did not present a legal question. You raised a valid layman's supposition that there might be a legal issue, then self-asserted you had asked a legal question, as if that made your point legitemate.
I specifcially addressed your claim, using the routinely accepted "assertions made without support do not require support when refuted".
Irrelevant. The time taken for a "typical vaccine" is conditioned by several factors:
- The time to administer vaccines in a series of trials that progressively elevate the numbers and range of the test subjects. This is the most important determinant for the authenticity of the testing process.
- How urgent the development requirement is.
- How much money is available.
- How many resources can be focused on its development.
Items 2 through 4 led to an unprecedented focus of money, expertise and all related resources. The stages of testing and the number of individuals involved were consistent with those for a "typical vaccine". Feel free to present data that contradicts this, but don't repeat the same trick of claiming I did not address your assertions.
Please refer to post 305.
I'm sorry if you are unfamilar with legal questions but I can't fix that. That is indeed the larger question facing our society, and the one with which legal minds are grappling now.
Please tell me you are familiar enough with emergency use authorization to understand that it CANNOT be granted if there is any drug currently in use that might treat the issue at hand. So...there could not be. Nothing would work. All conspiracy theories, along with the ridiculous lab leak theory.
EUA granted.
NOW, after the fact and millions of deaths and with approval process firmly in hand, they are
studying the drugs that were initially suggested that
might have saved the early millions.
From the
American Journal of Therapeutics, June 17, 2021: "
Moderate-certainty evidence finds that large reductions in COVID-19 deaths are possible using ivermectin. Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant impact on the SARS-CoV-2 pandemic globally."
If it were my grandma dying in the hospital, I would have wanted them to try Ivermectin, Hydroxycholoroquine or anything else that might save her early on. But no, it was inexplicably forbidden.
Well, except for this lady, whose family went to court for her after this politically motivated sequence of events:
"A 68-year-old woman with COVID-19, who has been in intensive care in an Illinois hospital for a month, started receiving the controversial drug
ivermectin (Stromectol) this week
after her family sued the hospital to have someone administer it, according to a report in the
Chicago Tribune.
...
On Friday, DuPage County Judge James Orel ruled Fype should be allowed to get the treatment.
Three days later, according to the
Daily Herald, the
lawyer for the hospital, Joseph Monahan, argued the hospital could not find a hospital-affiliated doctor to administer the ivermectin.
T
he Herald reported the judge told the hospital to "get out of the way" and allow any board-certified doctor to administer the drug.
When Fype's doctor was unable to administer it, the legal team found another doctor, Alan Bain, DO, to do it. Monahan said Bain was granted credentials to work at the hospital so he could administer it Monday evening.
In a follow-up hearing on Tuesday,
Monahan told Orel that the hospital asked 20 doctors and 19 other health care workers, including nurses and pharmacists, to administer the medication and they all declined, the
Herald reported."
Per her daughter via tweet, she improved and is still recovering as of May 21. I would move heaven and earth to get my mom treated with anything that might help if she were hospitalized.