Dr. David Martin has a very broad resume, some of which can reviewed in his webpage. His multi-faceted academic and professional background in both medical science (i.e., physiology and sports medicine) and business, combined with his extensive work with governments around the world gives him a unique understanding of the essentials of the Covid “PLANdemic”.
Perhaps because of his upbringing in a Mennonite family, he has a keen understanding of what is right in the sight of God. As he quoted in the Q&A below with Judy Mikovits, “Justice is Mine, saith the Lord” (Romans 12:19).
Given below are links to several series of videos featuring Dr. Martin that deal with aspects of the Covid situation, including his in-depth understanding of patents and timelines.
Fall 2021 – Bearing Down on the RICO Charges
In late October through early November, Martin is exposing his RICO charges against those that planned and those that maintain the Covid fraud. These videos are loaded chronologically newest first. As more videos appear from November 5 (Dallas TX) and 6 Lafayette, LA), they will be added to the list.
October 28, 2021 – Podcast
October 25, 2021 – Audio interview and transcript:
October 22/23 – We Can Act Conference, Salt Palace
September 29, 2021 – Interview with Dr. Joseph Mercola. Here are the video comments:
In this interview, we continue our coverage of the COVID “plandemic” by speaking to David Martin, Ph.D., who has done a phenomenal job uncovering the paper trail behind the virus now known as SARS-CoV-2. As it turns out, this is not a novel virus at all, as patents and government grants detailing key features of the virus go back two decades.
- In the early 2000s, David Martin, Ph.D., founder of M-CAM International, started finding large numbers of patents that violate biological and chemical weapons laws
- In 1999, Dr. Anthony Fauci 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
- Since 1999, at least 4,000 patents involving coronavirus have been filed, including patents detailing key features of the so-called “novel” SARS-CoV-2 virus
- The 2001 anthrax attack, which came out of medical and defense research, led to the passage of the PREP Act, which removed liability for manufacturers of emergency medical countermeasures
- The funds for entitlement programs and pensions will dry up by 2028, at which point the drug industry will go bankrupt as well. With a burgeoning population that is sick from the COVID jabs, we need to prepare new systems to care for each other
Here is the transcript of the above video
Dr. Martin’s Thoughts on the Covid Plandemic – Spring 2021
A brief admonition to people to not give in to demands to get the “shots”.
Given in this video is an interview with Atty. Reiner Fuellmich to aid in the building of cases for lawsuits and criminal prosecution of those committing “Crimes Against Humanity”, according to the Nuremberg Codes.
Investigative journalist Stew Peters interviews Dr. Martin about claims of “genocide” resulting what is termed the “Covid Plandemic”.
This video features Dr. Martin and Molecular Biologist Dr. Judy Mikovits at the late May 2021 “Free and Brave” conference at the Church of Glad Tidings in Live Oak, CA. Additional videos from that conference can be found here.
And this is Dr.Martin in another presentation at the same conference.
Dr. Martin was speaking at the Free and the Brave Conference, held at The Church of Glad Tidings in Live Oak, CA, north of Sacremento.
Dr. Martin Covid Plandemic Appearances – Summer 2021
Dr. Martin demonstrates how both the original synthetic Covid “virus” and the subsequent “vaccines” should all be considered bioweapons capable of great harm to many people.
At 8:12, the discussion turns to the August 23, 2021 FDA supposed authorization of the Pfizer “vaccine”. Dr. Martin outlines how the actual product that would be authorized has not yet been manufactured, and will not be available until 2023 at the earliest. Yet news media report that the Pfizer product is now approved. If so, why wouldn’t the FDA then also have ordered the Moderna and J&J products to be immediately taken off the market?
Note that after about 38 minutes, the discussion becomes more philosophical and no longer about Covid issues.
Dr. David Martin on Clay Clark’s Thrivetime Show, discussing some of the basics of the Covid Plandemic in a lighthearted yet serious manner.
Thinking out loud about the possibility that CRISPR’s latest “moves” might indicate the development of a second gene therapy to repair some of the damage done by the original Covid “shots”.
Interviews with Vaccine Choice Canada
In this interview with Vaccine Choice Canada, Dr. Martin discussed the culpability of PM Trudeau and others in Canada for a variety of Covid-related crimes as defined in Canadian law.
A blog entry from the VCC website discussing Dr. Martin’s interview.
A section of the full interview is found in this video:
The full interview is found here:
Book Detailing Covid Criminal Activity by Fauci and Others
From Amazon: World shocking evidence exposing big pharma and naming names in true crimes against humanity in preventative medicine. This vaccine patent and fraud research book free with limited edition collectible cover artwork by Stan Q. Upjohn. Dossier evidences medical crimes against humanity for financial gain of puppet masters. Dossier by Dr. Martin is fully released under a Creative Commons license CC- BY-NC-SA. For twenty years my company M·CAM has been monitoring possible violations of the 1925 Protocol for the Prohibition of the Use in War of Asphyxiating, Poisonous or other Gases and of Bacteriological Methods of Warfare (the Geneva Protocol) 1972 Convention on the Prohibition of the Development, Production, and Stockpiling of Bacteriological and Toxin Weapons and Their Destruction(the BTWC). In our 2003-2004 Global Technology Assessment: Vector Weaponization M·CAM highlighted China’s growing involvement in Polymerase Chain Reaction (PCR) technology with respect to joining the world stage in chimeric construction of viral vectors. Since that time, on a weekly basis, we have monitored the development of research and commercial efforts in this field, including, but not limited to, the research synergies forming between the United States Centers for Disease Control and Prevention (CDC), the National Institutes for Allergies and Infectious Diseases (NIAID), the University of North Carolina at Chapel Hill (UNC), Harvard University, Emory University, Vanderbilt University, Tsinghua University, University of Pennsylvania, many other research institutions, and their commercial affiliations. The National Institute of Health’s grant AI23946-08 issued to Dr. Ralph Baric at the University ofNorth Carolina at Chapel Hill (officially classified as affiliated with Dr. Anthony Fauci’s NIAID by at least 2003) began the work on synthetically altering the Coronaviridae (the coronavirus family) for the express purpose of general research, pathogenic enhancement, detection, manipulation, and potential therapeutic interventions targeting the same. As early as May 21, 2000, Dr. Baric and UNC sought to patent critical sections of the coronavirus family for their commercial benefit. In one of the several papers derived from work sponsored by this grant, Dr. Baric published what he reported to be the full length cDNA of SARS CoV in which it was clearly stated that SAR CoV was based on a composite of DNA segments. “Using a panel of contiguous cDNAs that span the entire genome, we have assembled a full-length cDNA of the SARS-CoV Urbani strain, and have rescued molecularly cloned SARS viruses (infectious clone SARS-CoV) that contained the expected marker mutations inserted into the component clones.” On April 19, 2002 – the Spring before the first SARS outbreak in Asia – Christopher M. Curtis, Boyd Yount, and Ralph Baric filed an application for U.S. Patent 7,279,372 for a method of producing recombinant coronavirus. In the first public record of the claims, they sought to patent a means of producing, “an infectious, replication defective, coronavirus.” This work was supported by the NIH grant referenced above and GM63228. In short, the U.S. Department of Health and Human Services was involved in the funding of amplifying the infectious nature of coronavirus between 1999 and 2002 before SARS was ever detected in humans. Against this backdrop, we noted the unusual patent prosecution efforts of the CDC, when on April 25, 2003 they sought to patent the SARS coronavirus isolated from humans that had reportedly transferred to humans during 2002-2003 SARS outbreak in Asia. 35 U.S.C. §101 prohibits patenting nature. This legality did not deter CDC in their efforts. Their application, updated in 2007, ultimately issued as U.S. Patent 7,220,852 and constrained anyone not licensed by their patent from manipulating SARS CoV, developing tests or kits to measure SARS coronavirus in humans or working with their patented virus for therapeutic use. Wake up and read this!
The book can be download from the following link: