A scientist, patriot, and truth-teller who exploded onto the alternative media scene when he was the featured scientist in filmmaker Mikki Willis’ excellent production: Plandemic InDOCTORnation. He exposed, for example, how the U.S. Government has owned patents on coronaviruses since the 1990s and that Covid was an intentional release, not a leak from a lab or a natural virus from bats. Dr. Martin has also named names by compiling a list titled “The Names of the People Killing Humanity” which includes the puppetmasters of Anthony Fauci, Rochelle Walensky, etc. such as Bill Gates, Klaus Schwab, Larry Page, Mark Zuckerberg, and several more.
Martin finished his doctorate at the University of Virginia in 1995, after which he was hired on to the medical school faculty in radiology and orthopedic surgery. In 2006, he set up the first medical device clinical trials organization for the University of Virginia — a company called IDEAmed — which conducted medical device clinical trials for U.S. Food and Drug Administration submission. So, he has an extensive background working with FDA clinical trials.
In 1998, he founded another company called M-CAM International, which is focused on finding ways to bring intellectual property into conventional finance. M-CAM also started auditing the U.S. patent system at the request of the U.S. Congress. In the early 2000s, M-CAM worked with the Senate Banking Committee and was a contractor for the United States Treasury to expose white collar criminal activity around intellectual property and tax fraud. In doing that work, Martin also discovered something else.
“Quite alarmingly, we found an enormous number of patents [detailing] biological and chemical weapon violations,” Martin says. “That was not something we were looking for. I let people know this was not something we set out to find. This is something that landed in our lap.
I developed a technology a decade earlier called linguistic genomics, which is a means by which you can look at unstructured text data and find the metaphoric meaning inside of what is being communicated. As you can imagine, if people of ill intent are trying to do something, they often hide what they’re doing in plain sight, but they use language that is not conventional.
So, when you find a patent, for example, on a blast-resistant pathogen from a rocket-propelled grenade — did you hear what I just said? ‘A blast-resistant pathogen from a rocket-propelled grenade.’ Does that sound like it’s a common way to inoculate a population or does that sound like [a bioweapon]?
And so, finding a number of bioweapons patents, we started taking into account some very serious things. I published once a year the literal global phonebook of every biological and chemical weapon violation that took place anywhere in the world.
[It tells you] the who, the where, the who funded it, what their addresses are. It was … used by U.S. law enforcement, intelligence communities and elsewhere around the world to track things that were being done inappropriately. And, it was in 1999 [that] we started detecting that there seemed to be an alarming event around coronavirus, which we’re going to get into.”
As explained by Martin, in 1999, the National Institutes of Allergy and Infectious Diseases (NIAID), headed by Dr. Anthony Fauci, identified coronavirus as a possible vaccine vector. At the time, the disclosed rationale was to try to come up with an HIV vaccine, and to that end, Fauci, in 1999, funded research to create “an infectious replication-defective recombinant coronavirus.”
In 2002, Ralph Baric, Ph.D. and colleagues at the University of North Carolina, Chapel Hill, filed a patent on recombinant coronavirus, and within a year, we got the world’s first SARS outbreak.
For more background on Fauci, be sure to read Robert F. Kennedy Jr.’s book “The Real Tony Fauci,” which details how Fauci’s promotion of AZT during the 1980s ended up killing hundreds of thousands of people. And the pattern we’re seeing with coronavirus is basically a repeat of previous behavior. Martin says:
“It’s important to realize that at the time [in 1984 when Fauci became director of the NIAID] we were transitioning from an STD environment in which syphilis and gonorrhea and those types of STDs were the things that we were concerned about …
HIV became a political and social hot potato because it was associated in many respects with lifestyle branding, and as a result it became a political issue to essentially identify a class of the population that could be the basis for research without consideration.
The notion by Fauci was that people with HIV had already made decisions that somehow entitled them to less humanity. As a result, the clinical trials around developing both management techniques as well as potential treatments … were done in a very reckless fashion. Numerous people died in [those] clinical trials, and by the way, still are …
He has been obsessed about this HIV situation as a platform to, essentially, use humans that he determines to be some form of sub-human for clinical trials. It is a horrific blight on the United States’ medical establishment that we have been willing to allow this to go on in the name of science, in the name of health promotion, since 1984, without any significant disruption or check.”
The First SARS Outbreak
The first SARS outbreak occurred in late 2002 going into 2003 in China. Curiously, before Baric’s team invented and patented a recombinant infectious replication-defective coronavirus, no one had ever heard of SARS.
“I’m not drawing a causal relationship,” Martin says. “I’m making an observation that humans and what we call coronavirus seem to have cohabitated this earth for hundreds of thousands of years.
And then we manipulate that [virus] in 1999. We start playing around with putting it into different animals and different human cell line models, and then in 2003, we have SARS. Like a lot of other things, it’s an observation worth noting.
What makes the observation more problematic, obviously, is this was happening during the unfortunate results of the 2001 anthrax attack, which as you know came out of federal labs …
[It] became very clear that this was not [due to] a bad actor, per se. This was medical and defense research gone bad that got into the public and people died. But the real benefit, if you will, of the anthrax attack was the passage of the PREP Act.”
Anthrax Attack Provided Desired Liability Removal
Inside the PREP Act we now have the carte blanche removal of liability for manufacturers of medical countermeasures. As noted by Martin, the PREP Act has “made pharmaceutical companies much more capable of instilling terror in the population, coercing a population into taking an untested measure, and doing so with absolute impunity.”
Curiously, while Martin’s annual report on bioweapons patents was, with only a few exceptions, appreciated and used by agencies around the world, when it comes to the information he has amassed on coronavirus, not a single agency anywhere in the world has been willing to address it.
“No one … seems to be willing to look at the fact that beginning in 2016 we started seeing very alarming language being used, which was ‘coronavirus poised for human emergence.’ This was in patents, but also in scientific publications. And when you start referring to a coronavirus allegedly poised for human emergence, after the World Health Organization has declared SARS eradicated, there’s something desperately wrong with that picture.”
Racketeering and Organized Crime
The biggest alarm bell was published February 12, 2016, by EcoHealth Alliance president Peter Daszak1 who, according to Martin, has been “the money laundering agent” for gain-of-function research coronaviruses after the U.S. implemented a moratorium on that kind of research in 2014. Rather than close it down, this research was simply moved over to China instead. In 2015, Daszak stated:2
“To sustain the funding base beyond the crisis, we need to increase the public understanding of the need for medical countermeasures, such as a pan influenza or a pan coronavirus vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process.”
That statement was made by Daszak in 2015, and was published in the spring of 2016. The statement “set off alarm bells very loudly within my organization,” Martin says, “because when you have somebody who is promoting gain-of-function research, and clearly blurring the line on what is even legal … saying we need ‘media to create the hype’ … and ‘investors will follow if they see profit’ … that doesn’t sound like public health.
To me, that sounds like organized crime. That sounds like racketeering, and we need to raise this issue.”
What the Coronavirus Patents Show
In all, since 2002, some 4,000 patents have been filed on the genome, vaccines and detection of coronavirus. According to Martin, this is alarming, “because you don’t file patents on something that you don’t intend to commercialize.” Evidence of intended commercialization can also be found by looking at the dates of certain patents by certain companies.
April 28, 2003, the U.S. Centers for Disease Control and Prevention filed a patent on the genome of the SARS coronavirus. Five days later, Sequoia Pharmaceuticals received a $935,000 grant and filed U.S. Patent 7151163 for a treatment for that same virus. How can you file a patent for the treatment of a virus that was only discovered five days earlier?
“That sounds like an inside job,” Martin says. “Because you cannot have a pathogen identified and a cure for it in five days, when all of the information was held from the public, because when the CDC filed its patent on the genome of coronavirus, it paid to keep that patent secret.
So, somebody somewhere knows that this thing was going to turn out to be a moneymaker … The proliferation of proprietary controls around SARS Coronavirus probably exceeds at least by two or three times most other pathogens …
Dana Farber had a monoclonal antibody patent system that came out of three NIH grants. Their patent 7750123 on the monoclonal antibody for SARS-Cov treatment took place in 2003.”
So, while we’ve been told that SARS-CoV-2 is something we’ve never seen before, there are 4,000 patents and patent applications that say otherwise. The same can be said for the testing and the COVID shots. For example, Pfizer filed the first S1 spike protein vaccine patent on coronavirus in 1990 — 30 years ago.
“Regardless of what part of the story we look at, the patent record is full of thousands of patents where commercial interests funded by NIAID and the National Institutes of Health have been building the economic cabal around coronavirus. This is not a new thing. It hasn’t been a new thing.
And regrettably, we’re being told continuously that somehow or another there’s something novel about this experience, despite the fact that every single part of what we are told is being detected with PCR … the injections, every single one of those things has been known and isolated for over 30 years.”
How Did We Get Here?
How did we get to a point where taxpayers are funding research on pathogens that are being designed to sicken and kill us, only to drive profits into the drug industry and all these various patent holders, which include the government itself?
In large part, it goes back to the implementation of the Bayh-Dole Act of 1980, which allows the beneficiaries of federal grants to file patents on work derived from federally funded research. The idea was that the economy would benefit by allowing scientists to be entrepreneurs first, rather than simply publishing their research.
This piece of legislation has undermined health care by bringing the patent office, the FDA and CDC into an unholy trinity that serves and promotes private pharmaceutical concerns. So, what we have now is an insidious funding loop. Martin explains:
“Corporations and pharma lobby to get people elected. Once they’re elected, the lobbyists flow an enormous amount of money into the various NIH programs. In the case of NIAID, since Fauci took over [in 1984], $191 billion have gone through his fingers. Now, is that because he’s successful?
No, as a matter of fact, under his watch, allergies and infectious diseases have increased over 60 times. Yet somehow or another, he’s still the director of a failed [agency] that’s gotten $191 billion to solve a problem that is getting worse every single year.
If it was a company, we would have fired him. The problem is, it’s not a company. It’s a money laundering agency. It moves public funds through the hands of a federal agency into the research laboratories, which ultimately are going to conduct research that is then licensed back to the benefactors, which are the pharmaceutical companies that paid to get people into office in the first place.
So, this is a revolving door problem, and the Bayh-Dole Act created an insidious incentive that said that the only research that was going to be conducted was going to be research that ultimately would flow back to the pharmaceutical industry and create juggernauts, where the risk of R&D was taken by the public and the benefit for that R&D was taken by the private. That’s a horrible thing, and that is exactly what Fauci has run.”
Why Did Fauci Pick Moderna as Vaccine Frontrunner?
Martin also points out that Fauci has also lied to Congress about the NIAID’s financial interests in drugs. During this pandemic, Congress and the Congressional Budget Office asked for an accounting of NIH-owned patents where they have potential commercial interest in the drugs being produced. Fauci did not disclose any of them. Instead he lied and said there are none.
“The evidence is stacked a mile long,” Martin says. “Moderna stands alone as the only recipient of NIAID funding that fails to comply with the law and fails to disclose the federal government’s interest in their intellectual property.
Despite the fact that everyone knew Moderna failed to disclose the federal government’s interest in its research, Fauci picked Moderna to be the frontrunner for an untested, commercially unsuccessful and entirely unproven mRNA vaccine technology in the spring of 2020.
There was no rational justification for that, and there would have been less rational justification, given the fact that Moderna is on record as having violated the federal law, the Bayh-Dole Act, 141 times at the time they were picked to be the winner.
This is a known fact, but it was overlooked entirely, and not a single law enforcement agent anywhere in the United States has decided that having a criminal organization supply a product sounds like a bad idea.”
Violations of Law Everywhere
Since the beginning of this pandemic, the number of rules, laws and regulations that have been broken in the name of public health boggle the mind. Even laws that are absolutely clear and in no way ambiguous are being broken. For example, under Code of Federal Regulations Title 21, section 50, no one can be forced or coerced into a clinical trial of an experimental medical product, even if it’s a pandemic countermeasure.
“It’s black and white, and this clinical trial does not end until 2023 in the first best instance. So, there is no such thing as an approved or even authorized use of a [COVID ‘vaccine’] that can be compelled on the population,” Martin says.
And yet they’re bribing, threatening and coercing people everywhere. The drug companies also violated basic principles by eliminating all of the controls and giving the test vaccine to everyone in the trials, leaving us nothing against which to compare side effects. They also do not have an independent investigational review board, or the statutorily required approval processes for the protocol.
The companies themselves decided to modify their protocols midstream, which simply isn’t how it’s done. Basically, we do not have an actual clinical trial on these COVID shots, because so many of the basic principles of clinical medical research were violated.
Collapsed Judicial System Has Put Big Pharma in Charge
The federal government is also violating the False Claims Act by telling you the COVID shots are safe and effective, when the studies are still years from being completed, and have been undermined in all the ways just mentioned.
“What we have is a situation where the deaths are actually considered to be acceptable,” Martin says. “I don’t know what world you have to come from to find that term even remotely speakable. I think the utterance of that phrase is horrific … We are killing people willfully, and we are doing it with impunity in the name of what we call a love affair with science.
The only problem is we’ve desecrated science in the process because it turns out that when I did randomized double-blind, placebo-controlled trials, you know what I had to do? I had to keep the populations blinded. I had to keep it placebo-controlled for the whole clinical trial. And the reason I had to do that is because that’s what the statute requires.
This entire process has been willful acts of harm to humanity. And the only hope we have is a very small note in the Department of Justice opinion that took place under the Trump administration, which says that if this was based on felony acts, then the entire emergency use authorization and all its benefits would collapse.
In other words, if we can show that a felony has occurred — racketeering, lying to Congress, the public coercion … [and] in the Fauci dossier3 I outline dozens of felony violations — [it] would bring this entire thing to its knees, because the moment the PREP Act protection falls away from Pfizer, Moderna, Johnson & Johnson, AstraZeneca and others, I can guarantee you [Fauci] will not be promoting a vaccine.
If they are liable for a single injury or death, they’ll pull the plug on what they know to be unsafe. That requires law enforcement to do its job. And somewhere there has to be a prosecutor who’s willing to do their job … Right now, I genuinely do not think we have three tiers of government. I don’t think there is a Department of Justice.
The judiciary is functionally gone … When we allow the judiciary to be an arm of the executive [branch], then what happens is we’ve actually lost the three-tiered structure of government. And, as a result, the system collapses. The judiciary was the only thing that was explicitly independent. We don’t allow judges to get sponsorship in campaign finance. We don’t allow judges to be elected.
We appoint them, we go through an approval process. We do all sorts of things to try to make sure the judiciary is independent. So, the only risk to the pharmaceutical industry, the only risk to an executive out of control, was the judiciary.
By collapsing the judicial system in the United States, we have effectively made the government a servant of its benefactors — and that is the pharmaceutical industry.”
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