In addition to understanding that the COVID plandemic was a product of satanic influence, many individuals also believe that Peter Marks is the government official most directly responsible for the entire COVID catastrophe. And understandably so, because when you look at Peter Mark’s contributions to the COVID plandemic (alone), you get to see that he reflects the systemic issues within the American and global healthcare bureaucracy that urgently need to be fixed, especially so as to disincentivise other health officials from following in similar footsteps. However, recent developments reveal that Peter Marks (as a former FDA official) does not only reflect what is wrong with healthcare bureaucracy, but also the problem with the revolving door corruption that occurs between regulators and the corporations they are supposed to hold accountable – which is precisely what we will address today.

PETER MARKS & THE FDA’S COVER-UP OF THE HARMS OF COVID JABS

Now, proceeding to look further into Peter Marks’ works at the FDA, many have been horrified to learn that the FDA and CDC systematically ignored every possible sign the COVID vaccines were dangerous as they pushed it on more and more people. One of the ways people were made aware of this was through the recently leaked recordings showing how stubbornly the head of FDA’s vaccine division, being Peter Marks at the time, refused to acknowledge any of the evidence brought forward by a group of permanently injured vaccine recipients, and even medical practitioners who were treating vaccine injured patients.

Here’s why this is important to note: generally, in looking through what transpired with the COVID-19 response, Anthony Fauci is commonly blamed for all that went amiss – and correctly so. However, we must not also miss the people who were also directly involved, while hidden within the FDA bureaucracy; and one such person is Peter Marks. Peter Marks is the primary person who covered up the reports of COVID vaccine injuries (and instead repeatedly told the world they were (quote unquote) “safe and effective”).

He was also the person who kept on pushing the FDA’s chief vaccine scientists (who were very pro-vaccine) to accelerate and condense the approval timelines for the COVID jabs (as those approvals were needed to legally implement Biden’s vaccine and booster mandates). The parties involved in this process, which included, Marion Gruber and Philip Krause (who were the Director and Deputy Director of the FDA’s Office of Vaccines Research and Review, respectively); they reported that there were (at that point) no more corners they could cut to further accelerate the COVID vaccine approvals, at which point they were removed from the COVID vaccine approval process and Peter Marks took it over (at which point the unjustifiable approvals and mandates quickly followed).

BUT, despite all of this, the media lied about Peter Marks. They stated that Marks was pressured to be anti-vax by RFK Jr. Yet, no single specific action is cited. Some articles even call Marks a hero, and he is praised by past FDA officials who now consult for drug companies or serve on their board. And funny enough, Peter Marks has now joined their ranks as one among those who embody the problem with the revolving- door corruption between the FDA and the corporations it is supposed to regulate – especially pharmaceutical companies.

FROM FDA REGULATOR TO ELI LILLY EXECUTIVE — THE REVOLVING DOOR OF CORRUPTION EXPANDS

More specifically, six months after his removal from the FDA’s Center for Biologics Evaluation and Research (CBER), Peter Marks has officially joined Eli Lilly — the same company that has become notorious for particularly employing former FDA officials. In any case, Marks will serve as Senior VP for Molecule Discovery and Head of Infectious Diseases, working alongside Rachael Anatol, who is another recently ousted regulator. Meanwhile, his former FDA counterpart Patrizia Cavazzoni also quietly landed at Pfizer as Chief Medical Officer earlier this year.

IN FACT, nine of the last ten FDA commissioners have actually gone on to work for major pharmaceutical companies shortly after leaving public office. Within the Bio-Pharmaceutical Complex, officials routinely rotate between government agencies, global NGOs, and Big Pharma — advancing personal careers while deepening institutional entanglements across the syndicate. And to paint a picture of both this corrupt revolving door relationship and also just how global this syndicate is.

Dr Elizabeth Nabel, who is the former Director of the National Heart, Lung, and Blood Institute (NHLBI) at the NIH — Joined Moderna’s Board of Directors. Dr Scott Gottlieb, who is the former FDA Commissioner — Joined the Board of Pfizer to promote vaccines on TV during pandemic. Dr Stephen Hahn, the former FDA Commissioner — Became Chief Medical Officer at Flagship Pioneering, which is the venture capital firm that launched Moderna. Sir Jonathan Van-Tam, who is the United Kingdom’s former Deputy Chief Medical Officer and member of the Vaccine Task Force — he was appointed as Senior Medical Consultant at Moderna. Then, Dr Jeremy Farrar, the former Director of the Wellcome Trust — he was appointed as Chief Scientist at the World Health Organization (WHO).

In addition, Dr Soren Brostrom, the Director General of the Danish Health Authority — he was also elected to the Executive Board of the World Health Organization. Then, Dr Moncef Slaoui, who is the former Chief Scientist of Operation Warp Speed — he previously served as an executive at GlaxoSmithKline (GSK) and as a Board member at Moderna. Dr Julie Gerberding, who is the former CDC Director — became President of Merck Vaccines, later serving as CEO of the Foundation for the National Institutes of Health (the NIH). There is also Dr Luciana Borio, the former FDA Acting Chief Scientist and member of the Biden COVID-19 Advisory Board — she became a Partner at ARCH Venture Partners, which is a firm heavily invested in biotech, while (as we just alluded) Dr Patrizia Cavazzoni, the former Director of the FDA’s Center for Drug Evaluation and Research (CDER) — Appointed as Chief Medical Officer at Pfizer, and Dr Peter Marks, the former Director of the FDA’s Center for Biologics Evaluation and Research (CBER) — has recently been appointed Senior Vice President for Molecule Discovery and Head of Infectious Diseases at Eli Lilly.

It is jarring how repetitive and global this revolving door corruption is; it is factually a syndicate that has gotten so bold in its endeavours, that it has become a network that erases the line between public health stewardship and corporate profiteering — which is a deeply embedded conflict of interest that undermines both trust and safety.

THE REVOLVING DOOR CORRUPTION IS INDICATIVE OF A BROADER ISSUE OF DIABOLICAL CORPORATIONS

Now here is why this revolving door issue matters beyond the specific individuals who are involved in it. A frequent criticism of corporations (which I believe also applies to governmental bureaucracies) is that their organisational structure encourages sociopathic behaviour – in fact, you would have heard me quote the President of Loveworld Incorporated, the highly esteemed Rev Dr Chris Oyakhilome DSc DSc DD, when he warned that “Capitalism has metamorphosed”, in that while we used to have corporations that sought to make profit through contributing products and services that added a net positive to society, that has since changed for a handful of them, and now they seek to make profit at the expense of the best interest of society.

Well, this typically occurs because MEMBERS of these entities are shielded from legal or personal accountability for their actions, with any wrongdoings being attributed to the corporation as a whole. In contrast, the main form of accountability most members face is the pressure to advance the institution’s mission (e.g., to make more money), leading to the proliferation of increasingly unethical methods to achieve that goal. To illustrate this, consider this quote from Peter Rost, who is a former executive at Pfizer and one of the few pharmaceutical leaders to speak out against the industry: He stated that (quote):

“It is scary how many similarities there are between this industry [speaking about the pharmaceutical industry] and the mob. The mob makes obscene amounts of money, as does this industry. The side effects of organised crime are killings and deaths, and the side effects are the same in this industry. The mob bribes politicians and others, and so does the drug industry … The difference is, all these people in the drug industry look upon themselves – well, I’d say 99 percent, anyway – look upon themselves as law-abiding citizens, not as citizens who would ever rob a bank … However, when they get together as a group and manage these corporations, something seems to happen … to otherwise good citizens when they are part of a corporation. It’s almost like when you have war atrocities; people do things they don’t think they’re capable of. When you’re in a group, people can do things they otherwise wouldn’t, because the group can validate what you’re doing as okay.”

Now, this genuinely sounds like a cry for help, from someone who fell into the pharmaceutical rabbit hole, only to discover later that they had become everything that they found morally reprehensible. Which clarifies, in part, how many of the people in this industry overlook what they know and are asked to do. But, on the other hand, we also know that there are those who are driven by their gain: be it power brockering or money. For instance, during the COVID plandemic, there was essentially zero daylight between Anthony Fauci’s agencies and the pharmaceutical industry; and this incestuous relationship was a significant part of the problem. But, here’s more on the propensity of pharmaceutical companies to function like the mafia or mob.

Furthermore, why this revolving door issue matters beyond the specific individuals who are involved in it is that it also points to a culture of disregard for morally acceptable or ethical conduct. In other words, pharmaceutical companies had a streak where they just did not fear consequences as much as they should, because they often got away with very heinous conduct – either through out-of-court settlements, or because of the work done through the pharmaceutical lobby. As such, this created a culture of outright corruption.

For instance, you’d recall that in May this year, the FDA Commissioner in this second Trump administration, being Dr Martin Makary, he publicly exposed a longstanding practice where agency inspectors accepted luxury limousine rides from the very pharmaceutical corporations they were tasked with overseeing. This underscores deep-seated conflicts of interest that have undermined the integrity of drug safety inspections, especially at overseas manufacturing facilities.

Now, the issue centers on foreign inspections, where the FDA’s oversight of drug production has historically relied on “scheduled” visits—essentially announced in advance. These setups, Makary argues, are “no inspections at all. They’re a joke.” Companies get ample time to polish their operations, hide violations, and even roll out the red carpet. Enter the limos: lavish rides provided by inspected firms, blurring the line between regulator and regulatee. While not outright bribes, such perks create an aura of favoritism, potentially softening enforcement. Makary’s exposure highlights how these rides were routine, eroding public trust in the FDA’s gold-standard claims. And this is not hyperbole; especially as the numbers paint a grim picture.

In particular, the FDA inspects thousands of foreign facilities annually, many in countries like India and China, which produce up to 80% of active pharmaceutical ingredients for U.S. drugs. A 2023 Government Accountability Office report flagged delays and weaknesses in these checks, exacerbated by COVID-19 travel bans. But post-pandemic, the return to fieldwork revealed these ethical lapses. In response, the FDA announced an expansion of unannounced inspections in May 2025, aiming to catch bad actors off-guard—those falsifying records or concealing contamination risks. The policy also explicitly bans inspectors from accepting industry-provided transport, including taxis, limos, or for-hire vehicles, alongside lodging perks. “This is a key step… to ensure that the FDA is the gold standard for regulatory oversight,

WORLD’S FIRST INTERNATIONAL GOVERNING BODY DECLARES mRNA INJECTIONS BIOLOGICAL & TECHNOLOGICAL WMDS

But, while all of this happens, there are strong efforts that are pushing against the works of pharmaceutical companies, and the vaccine holocaust. Notable among them is that in a stunning and historic move, the Alliance of Indigenous Nations (or A.I.N.) International Tribunal has issued an ORDER and DECLARATION stating that “mRNA nanoparticle injections are in fact biological and technological weapons of mass destruction.” And, of course, this marks the first formal judicial declaration by any recognized international authority categorizing the COVID-19 mRNA products as biological weapons.

Now, also important to note is that, in December 2024, Canada’s Ministry of Crown–Indigenous Relations and Northern Affairs (CIRNAC) formally acknowledged the Alliance of Indigenous Nations, its Treaty, and its International Tribunal—a judicial body composed of judges from every continent. In its official letter dated December 13, 2024, Canada affirmed that its relationship with the A.I.N. exists on a Nation-to-Nation basis, thereby recognizing the Tribunal as a sovereign legal authority under Indigenous and international law.

Also important to note is that the declaration by the Alliance of Indigenous Nations International Tribunal that the COVID vaccine is a biological and technological weapons of mass destruction aligns with our recent study by Zywiec et al, which demonstrated that the COVID-19 mRNA injections violate the Biological Weapons Convention, the Nuremberg Code, the Helsinki Declaration, and the US Constitution. It also aligns with Minnesota Bill HF3219, which classifies mRNA injections and related products as weapons of mass destruction under Section 609.712, prohibiting their possession or distribution within the state.

Written By Lindokuhle Mabaso