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

The medical industrial complex and scientistic cult evidently keep using the most vulnerable members of society (especially children) as a sacrifice in the pursuit of their efforts. But, with all that we know about the medical industrial complex, this is not news to anyone. In fact, what is expected is that there be progressive institutional reform in the status quo – especially in the second Trump administration – that directly challenges these issues. However, what is being exposed is just how deeply entrenched regulatory bodies are in their collusion with the medical industrial complex – especially pharmaceutical companies. But, today, we ought to discuss this further in light of Moderna’s mRNA COVID Shot getting Full FDA Approval for said to be “At-Risk” Infants.

U.S PRESIDENT DONALD TRUMP THREATENS 35% TARIFFS ON CANADA STARTING AUG. 1

U.S President Donald Trump has threatened a 35% tariff on goods imported from Canada. [ROLL CLIP00:11-] Trump’s announcement of higher tariffs on Canada comes amid a flurry of letters the U.S President has sent to world leaders over the past week informing them what rates their goods will be tariffed at come August 1, absent any trade deals.

BRAZIL VOWS RETALIATORY TARIFFS AGAINST US IF TRUMP FOLLOWS THROUGH ON 50% IMPORT TAXES

In a related matter, Brazilian President Luiz Inácio Lula da Silva has said that he will impose retaliatory tariffs on the United States if President Donald Trump follows through on a pledge to boost import taxes by 50% over the South American country’s criminal trial against his predecessor, Jair Bolsonaro. Lula said he will trigger Brazil’s reciprocity law approved by Congress earlier this year if negotiations with the U.S. fail.

NETANYAHU SAYS HOPING HOSTAGE DEAL WILL BE FINALIZED ‘IN A FEW DAYS’

On the last day of his 4-day trip to the US, Benjamin Netanyahu released a brief clip detailing his discussions with US President Donald Trump as well as Israel’s plans for Gaza amid ceasefire talks. Netanyahu emphasised Israel’s previous goals in Gaza including the removal of Hamas, demilitarisation of Gaza.

UK, FRANCE ANNOUNCE AGREEMENT ON PILOT MIGRANT RETURNS PROGRAM

British Prime Minister Keir Starmer and French President Emmanuel Macron have reached an agreement on a pilot programme to return migrants and refugees arriving in small boats, in a scheme to curb crossings over the English Channel. In a joint press conference on Thursday, Starmer said people arriving in the United Kingdom on small boats will “be detained and returned to France in short order”.

MODERNA’S mRNA COVID SHOT GETS FULL FDA APPROVAL FOR “AT-RISK” INFANTS

On July 10, 2025, the FDA granted full approval for Moderna’s mRNA COVID-19 vaccine (Spikevax) in “at-risk” children aged 6 months to 11 years. The shot was previously available only under emergency use authorization. This approval comes despite a mountain of evidence linking the shots to catastrophic harms, some of which include heart damage, brain damage, cancer, and mass death. Once again, this decision is quite concerning as it shows that regulatory agencies remain captured by the Bio-Pharmaceutical Complex. And so, one has to ask: How many more children must be sacrificed before accountability begins?

THIS MOVE COMPOUNDS THE LACK OF TRUST TOWARDS THE FDA

Now, this move certainly compounds the lack of trust towards the FDA, and necessarily so when you consider who influences the policy direction of the FDA. The general points of historical context to note regarding the FDA is that it was established in 1906 in response to public concern over unsafe food and drugs, such as spoiled food and counterfeit products. However, food industry lobbyists gradually gained influence, leading to the removal of the agency’s original leader. As a result, numerous harmful food additives were granted “generally recognised as safe” (GRAS) status and continue to be used today.

Then, in 1962, the FDA was given broad powers to oversee drug safety following the thalidomide incident. Unfortunately, the new regulations created strict standards for drug efficacy that were often selectively enforced, benefiting the pharmaceutical industry. Unfortunately, the FDA then increasingly targeted natural therapies, which led to many being erased from history – all of which is incredibly important to remember in light of our subsequent discussion on the propaganda against salt. Nevertheless, this historical context is why – despite the numerous attempts to reform the agency – issues of inefficiency and bias within the FDA persist. [PAUSE]

Now, evidence of the lobbyist factor in the FDA’s work, can be inferred in the agency’s work in food regulation. For instance, in the late 1800s, food producers were selling adulterated products, and pharmaceutical companies peddled medicines with secret ingredients like opium and alcohol. Public outrage grew, especially after exposés like Upton Sinclair’s ‘The Jungle’, which helped spark the 1906 Pure Food and Drug Act. This law gave the Bureau of Chemistry the power to ensure accurate labeling and prevent harmful additives in food.

Well, the director of the Bureau of Chemistry (and thus the first head of the FDA), Harvey Wiley conducted tests on food additives, proving they made healthy volunteers sick. While the public and many scientists supported his findings, the food industry fought back with powerful lobbyists and legal tactics. Well, Wiley’s book “The History of A Crime Against The Food Law” went on to detail much of the same abhorrent industry tactics we see happening now. But, this is all to detail the contextual background behind the FDA’s propensity to be influenced by lobbyists from the industries it is supposed to regulate – which is the first aspect of the FDA’s problem with corruption.

THE FDA’S DECEPTIVE AND HARMFUL “GENERALLY RECOGNISED AS SAFE” STATUS

Let’s then proceed to discuss the FDA’s “Generally Recognised as Safe” status. Many food additives are “generally recognised as safe” (or GRAS), and what this actually means is that they are widely used but WITHOUT REGULATION! Well, GRAS food products presented two fundamental issues: food industry counterfeiting and harmful additives. More specifically, the industry often fakes products to cut costs; for instance honey is often faked by adding cheap syrups or other ingredients to mimic its appearance and taste; while polluted waters are also added to enlarge oysters.

Now, despite evidence of harm, the food industry claimed these additives were essential for production, even though competitors showed higher-quality (and ultimately more profitable) products could be made without them. However, there were warnings that chronic exposure to additives could cause long-term health issues, such as organ damage; and these warnings were ignored – especially as the influence of industry lobbyists grew – which is why these harmful additives and faked foods were eventually reclassified as “generally recognized as safe.” But of course, these so-called “safe” additives have contributed to widespread chronic illness in society. Here’s more on the FDA’s GRAS status.

Furthermore, companies currently self-certify their chemicals without independent oversight; which has resulted in ingredients like titanium dioxide – which is banned in Europe and other developed nations still being legal in the US despite mounting health concerns. Through GRAS, FDA has for the longest time applied an “innocent until proven guilty” approach to food! Which is a categorically dangerous approach; ingredients should not have to harm or kill people first before they are deemed unsafe!

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

Let’s also look at vaccine cover-ups, as being part of the reasons behind the compounding lack of trust towards 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. 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).

THE PROBLEMS WITH THE FDA ARE FURTHER ENABLES BY STANDARDS IN MEDICINE

So, while the FDA is central to focus on as far as recent developments are concerned, it’s important also to note that the problems with the FDA are FURTHER enabled by standards in medicine. And I say that because it occurred to me that even if we have bad regulators who approve bad medicine, if we had good doctors and medical standards, then the harms could easily be averted or mitigated. But if the medical standard is overmedication and trusting “the science”, while doctors function as pharmaceutical representatives, then of course the problems are worse.

Let’s look at medical education. No matter how you dice it, medical education is quite challenging as there is simply too much to learn, and so even the “brightest” students adopt a triage mentality where they cut out things that NOTt necessary (or low-yield) (specifically) for exams so they can pass and get a degree. And because of this medical education typically presents 3 issues as far as medical standards are concerned.

First, the present standard of medical education covers many aspects in a superficial manner (e.g., med students just learn the classic indications, simple mechanisms of action and commonly recognized side effects of drugs). Now, this is quite problematic as many of those simplistic facts students memorize aren’t always entirely correct (or become evidently contradictory once you take the time to understand them). However, since students are under such pressure to memorize them, they take the facts as verbatim facts they don’t question and become quite haughty towards those who do.

Second, there has been a strong focus in medicine on the key medical products on the market (e.g., doctors focus on how to use pharmaceutical drugs along with the key microbes and their pharmaceutical treatments, understanding what aspects of the body each speciality is responsible for, how to interpret imaging studies, and even how to understand surgery well enough to want to go into it or refer patients to it). Similarly, there is also a strong focus on just the basic skills necessary for being a doctor (this includes being able to recognize potentially life-threatening conditions, conducting a physical exam with enough details to complete a medical note and writing billable medical notes). That said, there is also (thankfully) a strong focus on anatomy and physiology, which along with recognising key diseases and medical emergencies, represent some of the most valuable aspects of conventional medical training.

Then the third issue presented as far as medical standards are concerned has to do with how medical training cuts out a lot of the subtle aspects of medical science and doctoring that make you an effective clinician (and this includes things like medical ethics). And because of this, there is always a subset of medical students who have that inherent capacity and excel at being clinicians but very few learn it through their training. Put differently, standard medical training does NOT really cover what is needed to make people healthy as there is never enough time for that and again and again, we hear stories of medical educators who try to incorporate it but get pushed to the side due to limited curriculum time.

So, in a world where medical standards prioritise pharmaceutical interventions, and medical education and training focuses purely on passing exams as opposed to being more concerned with aspects of medical science that make a med student an effective clinician, well then of course the FDA’s corruption will have crippling impact, because doctors themselves are trained to push what the FDA has approved.

Well, no wonder the medical industrial complex is so-multilayered. There are clearly various actors involved. But, this also gives broader context behind why doctors become progressively less focused at making their patients better, while becoming product pushers for the pharmaceutical industry. Take this testimony from a pharmaceutical representative of 32 years. She exposes the corrupt relationship between big pharma and doctors, primarily based on greed because it was about organising expensive gifts and experiences for doctors in exchange for their product loyalty.

WORST OF ALL IS THAT PATIENTS ARE DISADVANTAGED BY THE MEDICAL SYSTEMS

I’ve had discussions with medical students and practitioners on the necessity of strict standards to enter medicine because it is one of those fields where there is no room for error. ANd I think many people still have that same perception of the medical field: which is that it brings in the best and trains them rigorously so they are less susceptible to making mistakes that can be the difference between life and death for some. BUT… while there absolutely are exceptions who are incredible doctors, it is also clear that the medical system is not as fool, corruption, and greed-proof as we thought. And worse of all is that there are many people who have not broken free from this presumption of excellence and efficacy in the medical field, and pay with their lives. And yet, the issues in medicine are quite nuanced because it is NOT just the FDA that has been financially bought out – it is almost everyone, down to the medical schools that teach the doctors that are supposed to practise evidence based and holistic medicine. In fact, the verdict from good doctors is that there is almost no such thing as evidence-based medicine anymore, in a world where big pharma has gained influence over regulators and academia.

Written By Lindokuhle Mabaso