VIDEO   Rechtsanwalt Dr. Reiner Füllmich
Verwendungszweck: “Spende Corona-Ausschuss”


below some parts in German, Dr Reiner, fast forward to David E Martin speaking in English



Reiner Fuellmich, Dr David Martin, Prof Martin Schwab, Dr Wolfgang Wodarg, Viviane Fischer

Reiner Fuellmich  00:00

Sorry, I have kept you waiting. It’s my fault. Are you still there?

Dr David Martin  00:04

Yes, I am.

Reiner Fuellmich  00:05

Oh, great. Nice to see you again.

Dr David Martin  00:07

Good to see you as well.

Reiner Fuellmich  00:09

So I think it’s best if you introduce yourself. I know you’re the chairman of M-CAM International Innovation Risk Management, but that doesn’t tell a whole lot of people what you’re really doing?

Dr David Martin  00:25

Yeah, well, from a corporate standpoint, we have since 1998, been the world’s largest underwriter of intangible assets used in finance in 168 countries. So in the majority of the countries around the world, our underwriting systems, which include the entire corpus of all patents, patent applications, federal grants, procurement records, E-Government records, etc. We have the ability to not only track what is happening and who is involved in what’s happening, but we monitor a series of thematic interests for a variety of organisations and individuals, as well as for our own commercial use, because as you probably know, we maintain three global equity indices, which are the top performing large cap and mid cap equity indexes worldwide. So our business is to monitor the innovation that’s happening around the world and specifically to monitor the economics of that innovation, the degree to which, you know, financial interests are being served, you know, corporate interests are being dislocated, etc. So, our business is the business of innovation and its finance.

Reiner Fuellmich  02:03

Reiner translates.  Okay, I got that. Yeah.

Dr David Martin  02:53

So, obviously from the standpoint of this presentation, as you know, we have reviewed the over 4000 patents that have been issued around SARS Coronavirus. And we have done a very comprehensive review of the financing of all of the manipulations of Coronavirus which gave rise to SARS as a sub clade of the beta Coronavirus family. And so what I wanted to do was give you a quick overview timeline wise because we’re not going to go through 4000 patents on this conversation but I have sent to you and your team, a document that is exceptionally important. This was made public in the spring of 2020. This document which which you do have and can be posted in the public record is  quite critical in that we took the reported gene sequence, which was reportedly isolated as a novel Coronavirus, indicated as such by the ICTV, the International Committee on Taxonomy of Viruses of the World Health Organisation, we took the actual genetic sequences that were reportedly novel and reviewed those against the patent records that were available as of the spring of 2020. And what we found, as you’ll see in this report, are over 120 patented pieces of evidence to suggest that the declaration of a novel Coronavirus was actually entirely a fallacy. There was no novel Coronavirus. There are countless very subtle modifications of Coronavirus sequences that have been uploaded, but there was no single identified novel Coronavirus at all. As a matter of fact, we found records in the patent records of sequences attributed to novelty going to patents that were sought as early as 1999. So, not only was this not a novel anything, it’s actually not only not been novel, it’s not been novel for over two decades. But let’s take a very short, and what I’ll do is I’ll take you on a very short journey through the patent landscape to make sure people understand what happened. But as you know, up until 1999, the topic of Coronavirus vs V [VSV?] the patenting activity around Coronavirus was uniquely applied to veterinary sciences. The first vaccine ever patented for Coronavirus was actually sought by Pfizer. The application for the first vaccine for Coronavirus, which was specifically this s1 spike protein. So the exact same thing that allegedly we have rushed into invention. The first application was filed January 28 2000, 21 years ago. So the idea that we we mysteriously stumbled on the the way to intervene on vaccines is not only ludicrous, it is incredulous because Timothy Millor, Sharon Klepfer, Albert Paul Reed, and Elaine Jones on January 28 2000, filed what ultimately was issued as US Patent 6372224 which was the spike protein virus, a vaccine for the canine Coronavirus, which is actually one of the multiple forms of Coronavirus. But as I said, the early work up until 1999 was largely focused in the area of vaccines for animals, the two animals receiving the most attention were probably Ralph Barics work on rabbits and the rabbit cardiomyopathy that was associated with significant problems among rabbit breeders, and then canine Coronavirus in Pfizer’s work to identify how to develop s and spike protein vaccine target candidates giving rise to the obvious evidence that says that neither the Coronavirus concept of a vaccine, nor the principle of the Coronavirus itself as a pathogen of interest with respect to the spike proteins behaviour is anything novel at all. As a matter of fact, it’s 22 years old, based on patent filings. What’s more problematic, and what is actually the most egregious problem is that Anthony Fauci and NIAID found the malleability of Coronavirus to be a potential candidate for HIV vaccines. And so SARS is actually not a natural progression of a zoonetic modification of Coronavirus. As a matter of fact, very specifically in 1999 Anthony Fauci funded research at the University of North Carolina Chapel Hill, specifically to create, and you cannot help but, you know, lament what I’m about to read because this comes directly from a patent application filed on April 19 2002. And you heard the date correctly 2002 where the NIAID built an infectious replication defective Coronavirus that was specifically targeted for human lung epithelium. In other words, we made SARS and we patented it on April 19 2002, before there was ever any alleged outbreak in Asia, which as you know, followed that by several months. That patent issued is US Patent 7279327. That patent clearly lays out in very specific gene sequencing, the fact that we knew that the ACE receptor, the ACE2 binding domain, the s1 spike protein, and other elements of what we have come to know as this scourge pathogen was not only engineered, but could be synthetically modified in the laboratory, using nothing more than gene sequencing technologies, taking computer code and turning it into a pathogen or an intermediate of the pathogen. And that technology was funded exclusively in the early days as a means by which we could actually harness Coronavirus as a vector to distribute HIV vaccine. I’ll let you translate that because that’s a lot of material.

Reiner Fuellmich  11:30

Okay. Reiner translates. Okay.

Reiner Fuellmich  15:32

(inaudible) Sequoia Pharmaceuticals.

Dr David Martin  15:32

Okay. So it gets worse. We were, my organisation was asked to monitor biological and chemical weapons treaty violations in the very early days of 2000. You’ll remember the anthrax events in September of 2001. And we were part of an investigation that gave rise to the congressional inquiry into not only the anthrax origins but also into what was unusual behaviour around Bayers ciprofloxacin drug, which was a drug used as a potential treatment for anthrax poisoning. And throughout the fall of 2001, we began monitoring an enormous number of bacterial and viral pathogens that were being patented through NIH, NIAID, US AMRIID, the US Armed Services Infectious Disease Programme, and a number of other agencies internationally that collaborated with them. And our concern was that Coronavirus was being seen as not only a potential manipulatable agent for potential use as a vaccine vector, but it was also very clearly being considered as a biological weapon candidate. And so our first public reporting on this took place prior to the SARS outbreak in the latter part of 2001. So you can imagine how disappointed I am to be sitting here 20 years later having 20 years earlier pointed that there was a problem looming on the horizon with respect to Coronavirus. But after the alleged outbreak and I will always say alleged outbreak because I think it’s important for us to understand that Coronavirus as a circulating pathogen inside of the viral model that we have is actually not new to the human condition and is not new to the last two decades. It’s actually been part of the sequence of proteins that circulates for quite a long time. But the alleged outbreak that took place in China in 2002, going into 2003 gave rise to a very problematic April 2003 filing by the United States Centre for Disease Control and Prevention. And this topic is of critical importance to get the nuance very precise, because in addition to filing the entire gene sequence on what became SARS Coronavirus, which is actually a violation of 35 US Code Section 101. You cannot patent a naturally occurring substance. The 35 US Code Section 101 violation was patent number 7220852. Now, that patent also had a series of derivative patents associated with it, these are our patent applications that were broken apart because they were of multiple patentable subject matter. But these include US Patent 46592703p, which is actually a very interesting designation, US Patent 7776521. These patents not only covered the gene sequence of SARS Coronavirus, but also covered the means of detecting it using RT-PCR. Now, the reason why that’s a problem is if you actually both own the patent on the gene itself, and you own the patent on its detection, you have a cutting advantage to being able to control 100 percent of the provenance of not only the virus itself, but also its detection, meaning you have entire scientific and message control. And this patent sought by the CDC was allegedly justified by their public relations team as being sought so that everyone would be free to be able to research Coronavirus. The only problem with that statement is it’s a lie and the reason why it’s a lie is because the patent office not once but twice rejected the patent on the gene sequence as unpatentable because the gene sequence was already in the public domain. In other words, prior to CDCs filing for a patent, the patent office found 99.9 percent identity with the already existing Coronavirus recorded in the public domain, and over the rejection of the patent examiner. And after having to pay an appeal fine in 2006 and 2007, the CDC overrode the patent offices rejection of their patent and ultimately in 2007 got the patent on SARS Coronavirus. Now, every public statement that CDC has made that said that this was in the public interest is falsifiable by their own paid bribe to the patent office. This is not something that’s subtle, and to make matters worse they paid an additional fee to keep their application private. Last time I checked, if you’re trying to make information available for the public research, you would not pay a fee to keep the information private. I wish I could have made up anything I just said, but all of that is available in the public patent archive record which any member of the public can review. And the Public PAIR, as it’s called at  the United States Patent Office, has not only the evidence but the actual documents which I have in my possession. Now, this is critically important. It’s critically important because fact checkers have repeatedly stated that the novel Coronavirus, designated as SARS CoV 2 is in fact distinct from the CDC patent. And here’s both the genetic and the patent problem. If you look at the gene sequence that is filed by CDC in 2003, again in 2005 and then again in 2006, what you find is identity in somewhere between 89 to 99 percent of the sequence overlaps that have been identified in what’s called the novel subclade of SARS CoV 2. What we know is that the core designation of SARS Coronavirus, which is actually the clade of the betacoronavirus family and the subclade that has been called SARS CoV 2 have to overlap from a taxonomic point of view. You cannot have SARS designation on a thing without it first being SARS. So the disingenuous fact checking that has been done saying that somehow or another CDC has nothing to do with this particular patent, or this particular pathogen, is beyond both the literal credibility of the published sequences. And it’s also beyond credulity when it comes to the ICTV taxonomy because it very clearly states that this is in fact a sub clade of the clade called SARS Coronavirus. Now, what’s important is on the 28th of April, and listen to the date very carefully because this date is problematic. Three days after CDC filed the patent on the SARS Coronavirus in 2003. Three days later, Sequoia Pharmaceuticals, a company that was set up in Maryland, Sequoia pharmaceuticals on the 28th of April 2003, filed a patent on Antiviral Agents of Treatment and Control of Infections by Coronavirus. CDC filed three days earlier, and then the treatment was available three days later. Now, just hold that thought for a second.

Dr David Martin  25:26

Well, there you go. That’s a good question because Sequoia Pharmaceuticals and ultimately Ablynx Pharmaceuticals became rolled into the proprietary holdings of Pfizer, Crucell, and Johnson and Johnson.

Reiner Fuellmich  25:43


Dr David Martin  25:45

So ask yourself a simple question. How would one have a patent on a treatment for a thing that had been invented three days earlier?

Reiner Fuellmich  25:55


Dr David Martin  25:57

The patent in question, the April 28th 2003 patent 7151163, issued to Sequoia Pharmaceuticals has another problem. The problem is it was issued and published before the CDC patent on Coronavirus was actually allowed. So the degree to which the information could have been known by any means other than insider information between those parties is zero. It is not physically possible for you to patent a thing that treats a thing that had not been published, because CDC had paid to keep it secret. This, my friends is the definition of criminal conspiracy racketeering and collusion. This is not a theory. This is evidence. You cannot have information in the future in form [for] a treatment for a thing that did not exist.

Reiner Fuellmich  27:16

This could well blow up into a Rico case, ultimately.

Dr David Martin  27:20

This is, it is a Rico case. It’s not could blow up into it, it is a Rico case. And the Rico pattern, which was established in April of 2003 for the first Coronavirus, was played out to exactly the same schedule when we see SARS CoV 2 show up when we have Moderna getting the spike protein sequence by phone from the vaccine research centre at NIAID prior to the definition of the novel subclade. How do you treat a thing before you actually have the thing?

Reiner Fuellmich  28:04

I have to translate this, you can’t make this up? Definitely not. Reiner translates.

Reiner Fuellmich  33:22

Yeah, well, it’s gonna get worse here.

Reiner Fuellmich  33:22

Oh no, it can’t get worse.

Dr David Martin  33:24

Oh it does. The 5th of June 2008, which is an important date because it is actually around the time when DARPA the Defence Advanced Research Programme in the United States actively took an interest in Coronavirus as a biological weapon. June 5 2008 Ablynx, which as you know is now part of Sanofi, filed a series of patents that specifically targeted what we’ve been told is the novel feature of the SARS CoV 2 virus. And you heard what I just said, this is the 5th of June 2008.

Reiner Fuellmich  34:09

They found what?

Dr David Martin  34:10

Specifically they targeted what was called the poly basic cleavage site for SARS Cov, the novel spike protein and the ACE2 receptor binding domain which is allegedly novel to SARS CoV 2, and all of that was patented on the 5th of June 2008. And those patents in sequence were issued between November 24th of 2015, which was US Patent 9193780. So that one came out after the gain of function moratorium. That one came after the MERS outbreak in the Middle East, but what you find is that then in 2016, 2017, 2019, a series of patents all covering not only the RNA strands, but also the sub components of the gene strands were all issued to Ablynx and Sanofi. And then we have Crucell. We have Rubius Therapeutics. We have Children’s Medical Corporation. We have countless others that include Ludwig Maximillans University in Munchen, Protein Sciences Corporation, Dana-Farber Cancer Institute, University of Iowa, University of Hong Kong, Chinese National Human Genome Centre in Shanghai, all identifying in patent filings that ranged from 2008 until 2017. Every attribute that was allegedly uniquely published by the single reference publication, the novel bat Coronavirus, reveals quote natural insertions of the s1 s2 to cleavage site of the spike protein and possible recombinant three origin of the SARS CoV 2 virus, the paper that has been routinely used to identify the novel virus. Unfortunately, if you actually take what they report to be novel, you find 73 patents issued between 2008 and 2019, which have the elements that were allegedly novel in the SARS CoV 2, specifically as it relates to the poly basic cleavage site based your receptor binding domain and the spike protein. So the clinically novel components of the clinically unique, clinically contagious, do you know where I’m going with this? Okay. There was no outbreak of SARS, because we had engineered all of the elements of that. And by 2016, the paper that was funded during the gain of function moratorium, that said that the SARS Coronavirus was poised for human emergence written by none other than Ralph Baric was not only poised for human emergence, but it was patented for commercial exploitation 73 times.

Reiner Fuellmich  38:07

Didn’t Ralph Baric, I think I saw a video clip with him giving a speech in which he explicitly told the audience that you can make a lot of money with this.

Dr David Martin  38:17

Yes you can. And he has made a lot of money doing this.

Reiner Fuellmich  38:22


Dr David Martin  38:25

So for those who want to live in the illusion that somehow or another that’s the end of the story, be prepared for a greater disappointment because somebody knew something in 2015 and 2016, which gave rise to my favourite quote of this entire pandemic. And by that I’m not being cute. My favourite quote of this pandemic was a statement made in 2015 by Peter Daszak. The statement that was made by Peter Daszak in 2015 reported in the National Academies Press Publication, February 12th 2016. And I’m quoting,” we need to increase public understanding of the need for medical countermeasures, such as 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”. end quote.

Viviane Fischer  39:47

That’s quite shocking, because I thought that –

Reiner Fuellmich  39:49

That’s really I mean, Peter Doshi, wasn’t he the one –

Dr David Martin 39:49

– let me just read that again, just because I don’t know if I might get lost in translation. So let me just go ahead and read it slowly. Yeah, and as Americans love to do When speaking to a multilingual audience, maybe I should say it louder. I won’t. “We need to increase public understanding of the need for medical countermeasures, such as 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.” End quote.

Reiner Fuellmich  40:45

– no no no Peter Daszak.

Viviane Fischer  40:46

Oh Daszak?

Dr David Martin  40:47

Peter Daszak the head of Eco Health Alliance?

Reiner Fuellmich  40:49

Peter Doshi is the good guy.

Viviane Fischer  40:51

Yeah, I was just –

Dr David Martin  40:52

– Peter Daszak the person who was independently corroborating the Chinese non lab leak non theory because there wasn’t a lab leak. This was an intentional bio weaponization of spike proteins to inject into people to get them addicted to a pan-Coronavirus vaccine. This has nothing to do with a pathogen that was released and every study that’s ever been launched to try to verify a lab leak is a red herring.

Viviane Fischer  41:26

And there’s really nothing that is new in this?

Dr David Martin 41:29

Nothing. Zero. 73 patents on everything clinically novel. 73, all issued before 2019. And I’m going to give you the biggest bombshell of all to prove that this was actually not a release of anything because Patent 7279327, the patent on the recombinant nature of that lung targeting Coronavirus, was transferred mysteriously from the University of North Carolina, Chapel Hill to the National Institutes of Health in 2018. Now, here’s the problem with that. Under the Bayh-Dole Act, the US government already has what’s called a margin right provision. That means if the US government is paid for research, they are entitled to benefit from that research at their demand or at their whim. So explain why, in 2017 and 2018, suddenly the National Institutes of Health have to take ownership of the patent that they already had rights to held by the University of North Carolina, Chapel Hill. And how did they need to file a Certificate of Correction to make sure that it was legally enforceable? Because there was a typographical error in the grant reference in the first filing. So they needed to make sure that not only did they get it right, but they needed to make sure every type of graphical error that was contained in the patent was correct. On the single patent required to develop the Vaccine Research Institute’s mandate, which was shared between the University of North Carolina, Chapel Hill in November of 2019 and Moderna in November of 2019 when UNC Chapel Hill, NIAID and Moderna began the sequencing of a spike protein vaccine a month before an outbreak ever happened.

Reiner Fuellmich  43:51

You have all the evidence, right?

Dr David Martin  43:53


Reiner Fuellmich  43:55

I’ll have to translate this. So it’s all about money.

Dr David Martin 49:25

It has always been about money, and just to answer a question that was asked slightly earlier. The script for this was written first January 6th 2004.

Reiner Fuellmich  49:39

January 6 2004? Who wrote the script?

Dr David Martin  49:42

Merck, at a conference called SARS and bioterrorism, bioterrorism emerging infectious diseases, anti microbials, therapeutics and immune modulators. Merck introduced the notion of what they called the new normal. Proper noun the new normal, which is the language that became the branded campaign that was adopted by the World Health Organisation, the Global Preparedness Monitoring Board, which was the board upon which the Chinese Director of Centre for Disease Control, Bill Gates’ Dr. Elias, of the Gates Foundation, and Anthony Fauci sat together on that board of directors. But the the first introduction of the new normal campaign, which was about getting people to accept a universal pan-influenza pan-coronavirus vaccine was actually adopted January 6th 2004. So it’s been around quite a long time. I’m not going to belabour many more points, other than to say that it was very clear that Merck knew that, sorry that Moderna knew that it was going to be placed in the front of the line with respect to the development of a vaccine in March of 2019. And this is a very important date, because in March of 2019, for reasons that are not transparent, they suddenly amended a series of rejected patent filings, which is a very bizarre behaviour, but they amended a number of patent filings to specifically make reference to an intentional or accidental release, I’m sorry, their term deliberate release of Coronavirus. So in March, they amended four failed patent applications to begin the process of a Coronavirus vaccine development. And they began dealing with a very significant problem that they had, which was they relied on technology that they did not own. Two Canadian companies Arbutus Pharmaceuticals and Acuitas Pharmaceuticals actually own the patent on the lipid nanoparticle envelope that’s required to deliver the injection of the mRNA fragment. And those patents have been issued both in Canada and in the US and then around the world in their World Intellectual Property equivalence. Moderna knew that they did not own the rights and began trying to negotiate with Arbutus and Acuitas to get the resolution of the lipid nanoparticle patented technology available to be put into a vaccine. And we know, as I made reference to before, that in November, they entered into a research and cooperative research and development agreement with UNC Chapel Hill with respect to getting the spike protein to put inside of the lipid nanoparticle so that they actually had a candidate vaccine before we had a pathogen, allegedly that was running around. What makes that story most problematic beyond the self evident nature of it is that we know that from 2016 until 2019, at every one of the NIAID Advisory Council board meetings, Anthony Fauci lamented the fact that he could not find a way to get people to accept the universal influenza vaccine, which is what was his favourite target, he was trying to get the population to engage in this process. And what becomes very evident with Peter Daszak Eco Health Alliance, UNC Chapel Hill and others, and then most specifically, by March of 2019, in the amended patent filings of Moderna, we see that there is a epiphany that says, What if there was an accidental or an intentional release of a respiratory pathogen? And what makes that particular phrase problematic is it is exactly recited in the book A World At Risk, which is the scenario that was put together by the World Health Organisation in September of 2019. So months before there’s an alleged pathogen, which says that we need to have a coordinated global experience of a respiratory pathogen release, which by September 2020, must put in place a universal capacity for public relations management, crowd control, and the acceptance of a universal vaccine mandate. That was September of 2019. And the language of an intentional release of a respiratory pathogen was written into the scenario that quote “must be completed by September 2020”.

Dr Wolfgang Wodarg  55:44

This was a text for Mrs. Brundtland was heading this commission, isn’t it?

Dr David Martin  55:50

Well, this is the global preparedness monitoring boards unified statement. There are a number of people who have taken credit and then backed away from credit for it, but yes, you’re right.

Dr Wolfgang Wodarg  56:00

Am I right too when I say that also the ACE2 receptor that was already described in the patents before 2019?

Dr David Martin  56:11

Yes, we have 117 patents with specifically the ACE2 receptor targeting mechanism for SARS Coronavirus.

Dr Wolfgang Wodarg  56:20

So because they always say this is the new thing with the virus.

Dr David Martin  56:24

Now, it’s not new, and it has not been even remotely new. It’s in publications going back to 2008. In the weaponization conferences that took place in Slovenia, in Europe, all across Europe, and all across the DARPA infrastructure. We’ve known about that since 2013. It’s isolation and amplification.

Viviane Fischer  56:49

And this, the amendment that Merck did to this, [where] they rejected patent applications, so was it only about the fact that it’s like deliberately, you know, like, put into the environment or something, or did they add anything else?

Dr David Martin  57:05

Well, these were four failed patent applications that were essentially revitalised in March of 2019. And it was Moderna, I misspoke. I spoke about Merck, it was Moderna, and I tried to correct that I’m sorry that that didn’t come through. But it’s Moderna’s patent applications that were amended in March of 2019 to include the deliberate release of a respiratory pathogen language.

Viviane Fischer  57:35

Was that not been rejected for some reason, they would just not they were just sitting there basically.

Dr David Martin  57:41

No, they do processes similar to other pharmaceutical companies, where they evergreen applications and continually modify applications to enjoy the earliest priority dates available. But that’s why you have to go back and look at the amendment of the application records to find out when the actual amendment language was put in place. But yeah, I mean, the fact of the matter is, and like I said, I’m not going to belabour all of the patent data, but any assertion that this pathogen is somehow unique or novel falls apart on the actual gene sequences, which are published in the patent record, and then more egregiously falls apart in the fact that we have Peter Daszak himself stating that we have to create public hype to get the public to accept the medical countermeasure of a pan-Coronavirus vaccine. And what makes that most ludicrous is the fact that as we know World Health Organisation had declared Coronavirus, you know, kind of a dead interest. I mean, they said that we had eradicated Coronavirus as a concern. So why having eradicated it in 2007 and 2008? Why did we start spending billions of dollars globally on a vaccine for a thing that had been eradicated by declaration in 2008? You know, kind of falls into the zone of incredulity, to say the least.

Reiner Fuellmich  59:23

Doesn’t that also mean if you if take the entirety of the evidence, then this is a tool the Coronavirus and the vaccines, this is a tool, and the interest of DARPA in creating a biological weapon out of this, this is a tool for everything else that latches on to this including population control, for example.

Dr David Martin  59:50

Well listen, we have to stop falling for even the mainstream narrative in our own line of questioning because the fact of the matter is this was seen as a highly malleable bioweapon. There is no question that by 2005, it was unquestionably a weapon of choice. And the illusion that we continue to unfortunately see very well meaning people get trapped in is conversations about whether we’re having a vaccine for a virus. The fact of the matter is we’re not, we’re injecting a spike protein mRNA sequence, which is a computer simulation, it’s not derived from nature. It’s a computer simulation of a sequence which has been known and patented for years. And what we know is that that sequence, as reported is reported across things like you know, the very reliable phone conversations that took place between Moderna and the vaccine research centre by self report, where I don’t know if you were on a phone call and you heard ATTCCGGTTCCGABBB, you know, is there any chance you might get a letter of valour a consonant dropped here or there. The ludicrous nature of the story that this is somehow prophylactive or preventative flies in the face of 100 percent of the evidence, because the evidence makes it abundantly clear that there has been no effort by any pharmaceutical company to combat the virus. This is about getting people injected with the known to be harmful s1 spike protein. So the cover story is that if you get an expression of a spike protein, you’re going to have some sort of general symptomatic relief. But the fact of the matter is, there has never been an intent to vaccinate a population as defined by the vaccination universe. And it’s important, I mean, let’s review just for the record, when Anthony Fauci tried desperately to get some of his quote, “synthetic RNA vaccines” published, he had his own patents rejected by the patent office. And I want to read what the patent office told him. When NIAID’s own Anthony Fauci thought that he could get an mRNA-like vaccine patented as a vaccine. And here’s the quote, “these arguments are persuasive to the extent that an antigenic peptide stimulates an immune response that may produce antibodies that bind to a specific peptide or protein, but it is not persuasive in regards to a vaccine.” Okay, this is the patent office. This is not some sort of public health agency. This is the patent office. “The immune response produced by a vaccine must be more than merely some immune response, but must also be protective. As noted in the previous Office Action, the art recognises the term vaccine to be a compound which prevents infection. Applicant has not demonstrated that the instantly claimed vaccine meets even the lower standard set forth in the specification, let alone the standard definition for being operative. In regards, therefore, claims five, seven and nine are not operative, as the anti HIV vaccine, which is what he was working on, is not patentable utility.” So Anthony Fauci himself was told by the patent office themselves, that what he was proposing as a vaccine does not meet the patentable standard, the legal standard, or the clinical standard.

Prof Martin Schwab  1:04:10

Oh, can we translate this for our audience? This might be very important.

Reiner Fuellmich  1:04:20

That is by the way, David, that is our friend, Martin Schwab, Professor Martin Schwab of, he’s our most important legal adviser from the University of Bielefeld.

Dr David Martin  1:04:34

Oh right.

Reiner Fuellmich  1:04:36

He is very smart. I know that, David I know a lot of our viewers are really shocked. I can see that from the responses. One of our viewers is our PCR test specialist, Professor Kemera. She can’t believe what’s going on here.

Dr David Martin  1:09:51

Well, the sad and sober irony is that I raised these issues beginning in 2002, after the anthrax scare, and the tragedy is we’re now sitting in a world where we have hundreds of millions of people who are being injected with a pathogen stimulating computer sequence, which is being sold under what the patent office, what the medical profession, and what the FDA and its own Clinical Standards would not suggest is a vaccine, but by using the term we actually are now subjecting hundreds of millions of people to what was known to be by 2005 a biological weapon.

Reiner Fuellmich  1:10:54

Reiner translates.

Dr David Martin  1:11:44

So I obviously have hundreds of hours of this stuff committed to memory because I’ve been doing it for two decades. But if you have any questions, I’d be happy to answer them.

Reiner Fuellmich  1:11:55

I’m sure there are going to be hundreds of questions, David. We’re going to be in touch. I think you’re going to be flooded by people, by people’s emails, etc. I’m just gonna forward what comes in or we’re gonna forward what comes in, but I do think, oh, yeah, we have a Martin Schwab, he probably has a really serious question.

Prof Martin Schwab  1:12:16

And after me Wolfgang too. Okay. I’m a legal Professor with the Faculty of Law here in Bieldfeld, I have to tell you that the constitutional Protection Units of the Ministry of Interior Affairs now observes the so called Corona denier scene. Corona denial is everyone who dares to disagree to the –

Reiner Fuellmich  1:12:54

– with the official line –

Prof Martin Schwab  1:12:55

– with the official line. Yes. Now. If this constitutional Protection Unit takes notice of me taking part in a discussion that this pandemic was put on stage intentionally, they will probably try to fire me from my job. So I have to at least ask some questions. While I heard you talking I took a look at patent number, oh which one was it, 7220852 and 7151163. And 7220852 was filed in April 12 and 715 and so on was filed in April 28 of 2004. I see a difference between 16, not 3 days, what did I misunderstand?

Dr David Martin  1:14:03

No. April 23rd 2003 was the CDC master filing date?

Prof Martin Schwab  1:14:09

Okay. Okay. I asked this question because if they try to make me go under for my job, I have to provide strong evidence.

Dr David Martin  1:14:22

Now we have all of this sent to, I know Dr. Fuellmich has the entire record in the Fauci dossier. 100 percent of this record is in there. The additional addendum that I sent across all has the records in there including all the priority filing dates as well as the issue date. So 100 percent of this is in written published records and you have the written records.

Prof Martin Schwab  1:14:26


Reiner Fuellmich  1:14:28

I have created my own file, and it’s labelled David Martin.

Prof Martin Schwab  1:15:00

Okay, there is, I did [an] analysis of media reportings here, and I can confirm that they give a very one sided account on the pandemic. Everyone who dares to declare the threat less dangerous than the government does will be denounced as conspiracy theorists, as sinful, and so on. So the media exactly did what you pointed out in the sentence you repeated twice before now. Actually, they tell us the story of the Delta variant, which is told to be much more contagious than everything else. Experts I have spoken to told me that the databases contain as many as more or 40,000 virus strains.

Dr David Martin  1:16:01


Prof Martin Schwab  1:16:02

So, could this delta variant be some kind of media hype you told us about before?

Dr David Martin  1:16:12

There is no such thing as an alpha or a beta or a gamma or a delta variant. This is a means by which what is desperately sought is a degree to which individuals can be coerced into accepting something that they would not otherwise accept. There has not been in any of the published studies on what has been reportedly the Delta variant, there has not been a population R not calculated, which is the actual replication rate. What has been estimated are computer simulations. But unfortunately, if you look at GISAID, which is the public source of uploading any one of a number of variations, what you’ll find is that there has been no ability to identify any clinically altered gene sequence, which has then a clinically expressed variation. And this is the problem all along. This is the problem going back to the very beginning of what’s alleged to be a pandemic, is we do not have any evidence that the gene sequence alteration had any clinical significance whatsoever. There has not been a single paper published by anyone that has actually established that anything novel since November of 2019, has clinical distinction from anything that predates November of 2019. The problem with the 73 patents that I described is that those 73 patents all contain what was reported to be novel in December in January of 2019, and 2020, respectively. So the problem is that even if we were to accept that there are idiopathic pneumonias, even if we were to accept that there are some set of pathogen induced symptoms, we do not have a single piece of published evidence that tells us that anything about the subclade SARS CoV 2 has clinical distinction from anything that was known and published prior to November 2019 in 73 patents dating to 2008.

Viviane Fischer  1:18:56

Could it be that the Delta variant sort of is that just the differences, you know that the clinical symptoms are the same, but that it has the, you know, the capability of like, infecting someone who’s already gone through variant B?

Dr David Martin  1:19:14

Well, so this is where we see an enormous amount of response and reflexive behaviour to media hype. There is no, and I’m going to repeat this, there is no evidence that the Delta variant is somehow distinct from anything else on GISAID. The fact that we are now looking for a thing doesn’t mean that it is a thing because we are looking at fragments of things. And the fact is that if we choose any fragment I could come up with, you know, I could come up with variant Omega tomorrow. And I could come up with variant Omega and I could say I’m looking for this sub strand of either DNA or RNA, or even a protein. And I could run around the world going, “oh, my gosh, fear the Omega variant”.

Prof Martin Schwab  1:20:15


Dr David Martin  1:20:16

And the problem is that because of the nature of the way in which we currently sequence genomes, which is actually a compositing process, it’s what we call in mathematics and interleaving. We don’t have any point of reference to actually know whether or not the thing we’re looking at is, in fact, distinct from either clinical or even genomic sense. And so we’re trapped in a world where unfortunately, if you go and look as I have at the papers that isolated the Delta variant, and actually ask the question, is the Delta variant anything other than the selection of a sequence in a systematic shift of an already disclosed other sequence? The answer is, it’s just an alteration, and when you start and stop what you call the reading frame. There is no novel anything. Yes, well,

Dr Wolfgang Wodarg  1:21:20

Dr Wolfgang Wodarg translates.

Reiner Fuellmich  1:28:41

David, I’ll make a long story very short. He’s in full agreement with your analysis. He understands your anguish with respect to you having told the world about this 20 years ago, almost. And he admires your tenacity. And he’s extremely grateful for you having taken this very close look at the problem through patent law. Dr Wodarg believes that patents are really problematic, because it turns out that it is probably five times more expensive to patent drugs, as opposed to having public I mean, not public, private, but public universities, getting the stipends getting the money that they need in order to develop these vaccines.

Dr David Martin  1:29:38

Yeah, I’m gonna do something that’s very unfair, but I’m gonna hold the document very close to the screen. And it’s only for representational purposes. But I want you to see that this the barrack patent that NIH needed to have returned to them for mysterious reasons in 2018, this is 7279327. And people can look this up on their own. But if you actually look at the sequences that are patented, which is one of the things that we’ve done, we actually look at the published sequences, and realise that depending on where you clip the actual sequence string, you will have the same thing or you’ll have a different thing based nothing more than on where you decide to parse the clip. And I want to read you, I mean, this is something that comes directly from their patent application. When they actually talk about the DNA strands, which they call sequence ID numbers. They actually specifically say the organism is an artificial sequence, an artificial sequence, meaning that it is not a sequence that has a rule base in nature, it is not something that was manifest for a particular natural derivative protein or natural derivative mRNA sequence that was isolated, every one of these is in fact a synthetic, artificial sequence. And if you go back and you look at each one of them, which we have done, what you’ll find is that the sequences, in fact, are contiguous, in many instances, but are overlapping in others, where it is merely a Caprice determination that says something is or is not part of an open reading frame, or it is or is not part of a particular oligonucleotide sequence. Now, the reason why that’s important is because if we are going to examine what ultimately is being injected into individuals, we need the exact sequence, not a kind of similar to, we need the exact sequence. And if you look at the FDA’s requirement, and if you look at the European regulatory environment, and if you look at the rest of the world’s regulatory environment, for reasons that cannot be explained, the exact sequence that has gone into what is amplified inside of the injection seems to be elusive, it seems to be something that someone cannot, in fact state with 100 percent certainty, the sequence is x. The problem that that presents is that at this point in time, as much as we can be told that there are, you know, clinical trials going on, and there are all sorts of other things going on, we have no way of verifying that a complete sequence has been, is, or potentially even could be manufactured into what ultimately becomes the lipid nanoparticle that is the carrier frequency into which the injection is delivered. And it’s important for people to understand that as far back as 2002, and all the way through the patent filings of 2003, and then the weaponization patents that began in 2008, in every one of these instances, fragments are identified, but they are identified without specificity. So we don’t have direct terminal ends of the fragments, we have fragments which have, you know, essentially hypothecated gaps into which anything can be placed. And that’s the reason why I find the fact checking around the patent situation to be most disappointing. Because the reason why fact checkers among their general lazy attributes, the reason why fact checkers are not actually checking facts when it comes to the patent matters is because the actual sequences are not represented in an digital form that makes it easy to do this comparison. We literally had to take images of submitted typed paper, and then code those in to do our own assessment. You cannot do this on the EPO’s patent site. You cannot do this with WIPO data from Geneva. You cannot do this with the US Patent Office data. You actually have to go in and reconstruct the actual gene sequences by hand and then you compare them to what has been uploaded on the public servers and that’s where you find that the question of novelty is something that was not addressed. This was a manufactured illusion.

Dr Wolfgang Wodarg  1:35:03

I have one more question. Is it possible that we see that the influenza has vanished is gone. We don’t have influenza anymore. The influenza for sure the viruses are also sequenced. And is it possible that those parts sequences we now speak about that they may exist in both of the virus types, so that it’s just a matter of testing and [a] matter of instruments to observe what we find, whether we find influenza, or whether we find Corona. If we have a certain, if you have a book, you have a word with five letters, and you will find this five letters in many books,

Dr David Martin  1:35:49

Right? Exactly. Yeah. Wolfgang, your question is a beautiful metaphor of exactly the problem. The problem is, if what we’re looking for is something we’ve decided we’ve decided is worth looking for, then we’ll find it. And the good news is we’ll find it [in] a bunch of places. And if we’ve decided that we’re no longer looking for a thing, it’s not entirely surprising that we don’t find it because we’re not looking for it. The fact of the matter is whether it’s the RT PCR tests that we decided that there are fragments, which by the way, I have looked at every one of the regulatory submissions, that has been submitted to the FDA, to try to figure out what was the gold standard to get the emergency use authorization. And what fragment of SARS CoV 2 was officially the official fragment that was the comparative standard. And the problem is that you can’t get a single standard. So the question becomes, in a world where there is no single standard, what is it that you actually find? Because if I’m looking for and why don’t I just read this? If I’m looking for a CCACGCTTTG? Do I add the next strand G or do I go no, no, the next bit is GTTTATTCG. And you get the point. The point is that where I choose to start and stop, I can actually say I found it. No, I didn’t find it.

Dr Wolfgang Wodarg  1:37:33


Dr David Martin  1:37:35

And I didn’t find the match that I projected on to the data because I chose to look at the data in a way that I could not find the match. Influenza did not leave the human population. Influenza was a failed decade long pan-influenza vaccine mandate that was desperately, desperately desperately promoted by governments around the world, they failed and they decided if influenza doesn’t deliver on the public promise of getting everybody to get an injection, let’s change the pathogen.

Dr Wolfgang Wodarg  1:38:19

There are many more they can change.

Dr David Martin  1:38:21

Oh, goodness, we’ve got tonnes more to come.

Reiner Fuellmich  1:38:24

Yeah, but now we’re on to them.

Viviane Fischer  1:38:27

I would like to tell you something about this development of the drosten PCR test, you know, because we looked at it just briefly, not to that extent that you now looked at the patents that you just described, but we looked at this kind of miracle, or like I mean, strange aspect of like the Drosten test development, because he, despite the fact that he would have needed to basically, through his employer, The Charite would be entitled to holding the patents on this, you know, his invention, he just published the instruction to the (inaudible) house so everyone could see it. So basically, the whole invention lost its possibility to be patented, and that’s kind of strange, you know, when you look at it, so we asked the Charite in a Freedom of Informatio act request, and so they said, Well, you know, because there was so much rush to get the, you know, this test out because there was this –

Reiner Fuellmich  1:39:34

– pandemic going on –

Viviane Fischer  1:39:34

– pandemic going on, so it was like, we didn’t look at the finances, you know, we just didn’t care. So that’s kind of strange as a procedure, because I mean, basically this test is worth like billions, you know, how could you just, I mean, this is a publicly financed hospital, how can they just give, you know, give away all this this whole thing, and then because he was also in close cooperation with a private company TIB Molbiol. It’s the same with which he had developed all the PCR tests from 2002 from the first SARS, and then MERS, (inaudible) and so on and so on. So it’s very strange, you know, because he was basically like, functioning as a door opener for this company, you know, because they also said to us, so basically, it was Drosten who decided to which possible country or like laboratory or whatever the test, this TIB Molbiol company would send out the test kits in order to then of course, make more money, because he was basically like, he had a first mover advantage, you know, Drosten and or this company. So it’s clear now, I mean, maybe there was nothing at that point, because there was so many patents already going on. So basically, from this not novel virus or a PCR test, he couldn’t patent anything that would have been new. So basically, it was really like a very logical thing to do then to use the whole thing as a just to, you know, make profit from this first mover advantage. And maybe Drosten is somehow involved in this whole legal scam, financial –

Reiner Fuellmich  1:41:16

– oh he’s one of the most important people in this game, because he’s the one who’s strings they pulled first.

Dr David Martin  1:41:22

Yeah, you need you need to create the illusion of demand, and there’s nothing right now that does a better job of creating the illusion of demand than the urgency of an event that you’ve manufactured.

Reiner Fuellmich  1:41:43

This sounds almost like comedy, but it is not.

Dr David Martin  1:41:47

Well, it is in that we have to realise that part of the reason why it was so easy for us to monitor and track this particular, you know, campaign of coercion and terror is because we’ve done it before. You know, I started my comments by making sure people remember that when it came to solving for the anthrax outbreak. Now remember, that while we had hundreds of 1000s of military people in the Middle East, allegedly getting even for the events of September of 2001, we had two Postal Inspectors investigating anthrax. Two! The largest alleged bioweapons attack on US soil and we had two Postal Inspectors. You can’t genuinely believe that two Postal Inspectors are the, you know, the crime stopping, you know, mind bendingly powerful individuals in the universe. Now I have nothing against Postal Inspectors, but I can guarantee you that if I was investigating a bioterror attack, I would not have the post office, having two Postal Inspectors as their crack team, doing the investigation. You know, it was disingenuous, and Congress knew it. And that’s the reason why, you know, we publish a thing that is not necessarily a bestseller, but we publish an intelligence briefing on every violation of the biological and chemical weapons treaties that people have signed around the world. And it’s a phone book that tells you where and who and who’s funding, and so for us it wasn’t hard to figure out that this was not a public health crisis. This was an opportunistic marketing campaign to address a stated objective, and that’s why this is occams razor. It’s the easiest thing to describe, because they’re the ones that set it. And the occams razor reality is they said they needed to get the public to accept a pan-Coronavirus vaccine countermeasure, and they needed the media to create the hype, and investors would follow where they see profit. You do not have anything else you need to rely on to explain the events of the last 20 months, than the actual statement of the actual perpetrator. And I don’t do the navel gazing exercise of going in to try to understand whether there were mommy issues behind a bank robber if they’re holding a bag of money outside of a bank. I actually make the crazy assumption that maybe they’re a bank robber. Similarly, if I have somebody who says we need to use the media to hype a medical countermeasure, which is in fact the injection of a synthetic, recombinant chimeric protein developed off of a computer simulation. If I’m actually going to listen to the motivation for why that might be being done, I will listen to the person doing the manipulation who says investors will follow where they see profit? I don’t need more explanation.

Reiner Fuellmich  1:45:28

Me either. Okay, this is mind boggling. I’m really glad, David, [I mean] we spoke a couple of months ago, maybe 3 or 4 months ago, and we were introduced to each other by a David, I’m sorry, James Henry.

Dr David Martin  1:45:52


Reiner Fuellmich  1:45:52

And I was trying to find patent lawyers in this country who might be interested in this case. Now, there are a few patent lawyers who understand about it, but there’s no one apparently up till now, but maybe this is going to change. But there was no one willing to tackle this in the context of Corona. That’s the problem.

Dr Wolfgang Wodarg  1:46:17

This is not new. I’ve tried to find such a lawyer to specialise on patents for the (inaudible) Commission for the German Bundestag 10 years ago, or more than 15 years ago. And we did not find because they were afraid to be critical on the system. They would destroy their own job. This was very difficult.

Reiner Fuellmich  1:46:38

Yeah, bear in mind that this is an old problem, because that, here’s where the problem comes in. Ever since the establishment of the European Patent Office, the Germans and the French, not surprisingly, have maintained animosity that has, you know, been just this newest version of animosity that goes back centuries. But when the EPO was set up, the role of the patent office in Munich became a very nationalistic issue for Germany. And the notion that German patent examiners and German patent professionals still enjoyed supremacy over the rest of Europe became dogmatic. In 2003 in 2004, when the European Patent Office was first audited by my organisation, and where we showed that somewhere between 20 and 30 percent of the patents in Europe, were functional forgeries, meaning that they were copied from previous patents, that the German representation of the European Patent Office lost their mind at the notion that they were doing anything remotely wrong. When the European Union commissioned us to do an examination into software patents a few years later, at the request of the Swedish delegation to the European Union, and we showed hundreds and hundreds of software patents which were illegally granted by the European Union through the EPO. And then we found out that it was German patent examiners and German patent practitioners who were the ones who were responsible for their filing. We once again saw that there was an enormous outcry. And so what happens is that we have a dogmatically held position, which says that even though the European Patent Office is supposed to be pan European, there is still in the minds of the German patent establishment, a supremacy over the rest of Europe. And if you call into question anything, including patents granted on a bio weapon, you are treading on ground that there is no forgiveness for.

Dr Wolfgang Wodarg  1:49:09

Yes. We had some questions from Transparency International, and we were wiped out; the topic was not followed.

Dr David Martin  1:49:17

Yep. You just can’t. It’s not accessible, and that’s just the tragedy of what has unfortunately become a a regulatory capture organisation. It’s actually not doing the public service.

Reiner Fuellmich  1:50:24

Reiner translates.

Dr David Martin  1:50:53

Well, thank you for the time that you’ve spent and I hope that it was helpful.

Reiner Fuellmich  1:50:57

It was very helpful.

Dr Wolfgang Wodarg  1:50:59

Very helpful, thank you very much.

Reiner Fuellmich  1:51:00

We’re gonna hear a lot of echoes. Thank you David, and have a great weekend.

Dr David Martin  1:51:07

Okay, Take care everybody.

Dr David Martin  1:51:08

Yeah, you too. Bye bye.

Viviane Fischer  1:51:10


Dr Wolfgang Wodarg  1:51:11

Bye bye.

Dr Reiner Fuellmich 1:51:11

All conversing in German.