By Belle Carter
The Food and Drug Administration (FDA) adopted back in June a “Future Framework” scheme that allows Pfizer and Moderna to reformulate and release updated Wuhan coronavirus (COVID-19) shots without conducting any additional clinical trials.
Pharmaceutical companies will be able to update their current COVID-19 jabs to include “an omicron BA.4/5 spike protein component to the current vaccine composition to create a two-component (bivalent) booster vaccine.” The modified versions are expected to be available as boosters in time for the “cold and flu” season. (Related: FDA’s “Future Framework” allows Big Pharma corporations to unleash reformulated covid vaccines without any clinical trials.)
The scheme will not only permit completely untested, modified experimental COVID injections to be produced in massive amounts, but it could also be expanded to other vaccines and drugs. This was according to an analysis published by Dr. Joseph Mercola in his newsletter.
“It could even lower standards for drug trials in general, which historically have required at least 10 years of multi-phase testing,” he wrote, stressing that this is the worst idea in the history of public health.
He further cited political economist Toby Roger’s Substack article explaining the origin and purpose of this dangerous move by the FDA.
Rogers said that everyone now knows that the mRNA COVID-19 shots do not stop infection, transmission, hospitalization or death from the SARS-CoV-2 virus. However, Pfizer and Moderna are making about $50 billion a year on these shots and so they want that to continue. To do this, they would need to reformulate the shots, maybe target a new variant or change some of the ingredients.
“Since reformulated shots mean new clinical trials and new regulatory review by the FDA, there is a decent chance that any reformulated shot might fail new testing and the public is deeply skeptical of these shots so the scrutiny would be intense. So, Big Pharma figured out a way to use regulatory capture to get their reformulated COVID-19 shots approved without further clinical trials,” he pointed out.
Mercola further said the people have seen plenty of examples of how vaccine trials are being rigged and that the “framework” is an extreme expansion and formalization of that rigging.
“Not recording injuries, or recording them improperly, is a common tactic used to fudge results and make a vaccine appear safer than it is. Another common strategy is to exclude any parameter that turns out to be problematic, and that includes participants who are injured. Because this is such a common trick, the fact that 3,000 of the 4,526 children (aged six months through four years) enrolled in Pfizer’s pediatric COVID trial were excluded is a huge red flag,” he said.
Rogers: WHO, Gates Foundation could be behind the scheme
According to Rogers, the World Health Organization (WHO) and the Bill & Melinda Gates Foundation could be the masterminds behind the scheme.
“Gates requires that WHO use the McKinsey consulting firm so this is probably a McKinsey operation (and McKinsey also works for Pharma so this is a huge conflict of interest). As Naomi Wolf points out, the involvement of the WHO also raises troubling questions about the influence of the Chinese Communist Party over this process,” he wrote.
He further stated that as far back as January, the WHO, Gates and McKinsey junta realized that these shots were terrible and so they decided to use that as an opportunity to seize even more power and control.
“The WHO set up the Technical Advisory Group on COVID-19 Vaccine Composition [TAG-CO-VAC] to implement these Orwellian ‘Future Frameworks’ to lower manufacturing costs for Pharma and avoid bothersome health data that might hurt profits. All the messaging we have seen from the FDA and leaked to the press was initially developed and released by TAG-CO-VAC.”
Back in June, the FDA released an 18-page briefing document in connection with this scheme.
“To base the entire future of COVID-19 shots on this glorified undergrad term paper is madness,” Rogers said. He noted that the briefing document literally states that the evaluation will need to rely on measures other than actual health outcomes because of time constraints.
Watch the below video where Toby Rogers talks about how FDA’s “Future Framework” is a reckless plan.
This video is from the Chinese taking down EVIL CCP channel on Brighteon.com.