It seems the White House intends to strongarm the Food and Drug Administration (FDA) into fully approving COVID vaccines, while completely dismissing evolving safety and efficacy concerns in the process.
It began during a CNN town hall this week, when President Biden appeared to let it slip (in difficult to comprehend language) that he was pushing for full FDA approval before the end of the year.
Fully authorizing the COVID vaccines will allow for the government to hop over legal and regulatory hurdles that come from their current status under emergency use authorization. The Biden Administration seems to believe full approval will act as a mandate for further draconian, top down policies from the federal government, the likes of which may include vaccine passports and compulsory vaccination for much of public and private industry.
In an article earlier this week, state-corporate press organ NBC News attempted to tee up the case for vaccine mandates. Several Obama and Biden “health” officials went on the record for the piece to make it clear they wanted to make life as difficult as possible for “unvaccinated” Americans.
“The official regulatory sign off would remove a significant legal and public relations barrier for businesses and government agencies that want to require vaccinations for their employees and customers, former health officials from the Biden and the Obama administrations said,” the NBC article states.
Andy Slavitt, a former Biden Administration official who infamously advertised a mask that he claimed could “deactivate” the coronavirus, told NBC News:
“I think once the vaccines go through full FDA approval, everything should be on the table, and I think that everything will be on the table at the level of municipalities, states, employers, venues, government agencies.”
The FDA is not in fact an independent regulatory agency. It is simply another executive branch agency that falls under the umbrella of the Department of Health and Human Services. While the FDA is tasked with ensuring the safety of drugs that have prospects for the open market, the reality remains that politicians and pharmaceutical companies regularly steer and manipulate the FDA as they please.
The revolving door between Big Pharma and the Government Health is very much on display at the FDA today. Patrizia Cavazzoni, the FDA’s new top drug regulator, worked for two decades in Big Pharma (including a stint at Pfizer) before entering her government role in 2019. In fact, it is the norm, not an aberration, for Big Pharma executives to have a resume stuffed with Big Pharma consulting and employment gigs. Recent FDA chiefs, such as Pfizer board member Scott Gottlieb and Obama FDA chief Robert Califf, have resumes stuffed with examples of the constant revolving door between lobbying, government, and pharmaceutical companies.
The notion that mRNA vaccines have proven, *long term* safety and efficacy standards for the masses is simply not possible to prove at this time. Real world data (as opposed to Big Pharma studies) out of Israel, Malta, the UK, and elsewhere show that the vaccines have not exactly demonstrated much of an ability to prevent infection, contrary to the early claims made by pharmaceutical companies and Government Health institutions.
The bottom line: The White House is seeking to use the reputation of the FDA to force more Americans to take COVID vaccines, and they’ve made it clear that this is entirely about politics, and not science. The government agency that gave us the disaster that is the food pyramid is not an independent body, nor is it any kind of authority on science and health. The FDA is just another bureaucracy, with the primary interested parties being the White House and Big Pharma.
Reprinted with permission from The Dossier.