Four American war criminals I think should be prosecuted first: Alex Azar, Robert Kadlec, Marion Gruber and Bill Gates
Four American war criminals I think should be prosecuted first: Alex Azar, Robert Kadlec, Marion Gruber and Bill Gates
Four American war criminals I think should be prosecuted first: Alex Azar, Robert Kadlec, Marion Gruber and Bill Gates
A reader commented at yesterday’s post In Nov. 2020, Pfizer told FDA reviewers, led by Marion Gruber, that safety studies were neither needed nor conducted; in making that argument, Pfizer cited WHO guidance written in 2002 by a team led by Marion Gruber:
I am bothering Robert F. Kennedy Jr. and Mary Holland [attorneys at Children’s Health Defense] re this post and suing Gruber.
I poked around in my index card files a little more, looked a little more at Marion Gruber’s 12/11/2020 Pfizer EUA review memo, and located Alex Azar’s 03/24/2020 Declaration of Emergency Use Authorization: “that circumstances exist justifying the authorization of emergency use of medical devices, including alternative products used as medical devices.” 85 Federal Register 17335.
I think the top three American government officials to be prosecuted for treason (18 USC 2381), biological weapons development, stockpiling and use (18 USC 175), terrorism (18 USC 2331), war crimes (18 USC 2441), genocide (18 USC 1091), and related crimes, should be Marion Gruber, Robert Kadlec and Alex Azar, based on the paper trail of intentionally fraudulent, malicious and homicidal declarations and authorizations they issued under PREP Act and EUA laws.
The first American civilian to be prosecuted for the same crimes should be Bill Gates, on the basis of the Microsoft patent US 16138518, "cryptocurrency system using body activity data."
Because I noticed another key timeline sequence today.
The patent for systems to install nanotech in living human beings was issued 03/26/20, two days after Alex Azar on 03/24/2020 issued a Declaration of Emergency Use Authorization for the general class of products, that Marion Gruber in December 2020 began authorizing for actual use on humans under specific manufacturing brands including Pfizer, Moderna and Janssen, falsely presented to the public as 'Covid-19 vaccines.'
They are actually injectable nanotech devices whose precise contents and biological effects have been made known to the public only through the cardiac, neurological, reproductive and other injuries and deaths directly experienced by millions of recipients.
And have only been scientifically investigated by independent researchers, using smuggled vials, working on at least 26 teams in 16 countries on five continents between July 2021 and August 2022, as collected by David A. Hughes in the International Journal of Vaccine Theory, Research and Practice, Sept. 3, 2022 issue.
HHS Secretary Alex Azar issued the original declaration that a public health emergency exists 01/31/2020, retroactive to 01/27/2020. The declaration showed up in the Federal Register as effective 02/04/2020, along with a declaration for emergency use authorization of in vitro diagnostics (PCR tests). 85 Federal Register 7316.
In coordination with Robert Kadlec, the HHS Assistant Secretary for Preparedness and Response (ASPR), Azar then issued A Declaration Under the PREP Act for Medical Countermeasures Against COVID–19 on 03/10/2020, retroactive to 02/04/2020, providing all the people in the research, development, supply, distribution and administration chain with blanket immunity from legal liability for their personal actions.
Kadlec then submitted a request for a Declaration of Emergency Use Authorization to Azar, who issued it on 03/24/2020, declaring “that circumstances exist justifying the authorization of emergency use of medical devices, including alternative products used as medical devices.”
From February 2020 forward, Pfizer/Moderna/Janssen/DOD/DARPA/BARDA and subcontractors ran the fraudulent non-clinical, pre-clinical and clinical trials that whistleblower Brook Jackson discovered in September 2020 and immediately reported to the FDA, including Marion Gruber, Director of HHS-FDA-Center for Biologics Evaluation and Research, Office of Vaccines Research and Review.
Gruber blocked Jackson’s reports and refused to investigate, and then personally authorized the mass injection program — actual use of the injectable products on living human beings— under EUA on 12/11/2020 (Pfizer/BioNTech); 12/18/2020 (Moderna); and 02/27/2021 (Janssen).
Sage has a new post about Robert “Swings-Both-Ways” Malone:
https://sagehana.substack.com/p/genocide-clue-solving-the-murder
I posted a comment there, reposted here:
“You kind of can't have it both ways.”
That “both ways” problem has been preoccupying me today, while I ponder what information would go in the Statement of Facts section of a federal civil complaint charging Azar, Kadlec, Gruber and Gates with the terrorism and related genocide/murder/conspiracy/war crimes under 18 USC 2333.
I think the challenge for the federal courts — should they stand up for the Constitution-in-exile and the rule of law derived from it — is to untangle the two, parallel, non-intersecting statutory threads that have unspooled since about 1938 and then got tangled together in a horrific knot in January 2020.
Under one thread, which includes things like the PATRIOT Act, the Project BioShield Act, and the PREP Act, the US government actions by DOD/HHS/DHS/DOJ were legitimate public health measures undertaken to cope with a legitimate public health threat, and the people who performed them are heroes who saved the world with modern medical technology.
Under the other thread, which includes things like the 1990 Biological Weapons prohibition law that Francis Boyle wrote, and the 1993 Religious Freedom Restoration Act, the same people were state-sponsored terrorists who destroyed informed consent on their way to world domination.
The way to resolve the dispute is to gather and present the evidence and make arguments for and against each claim, in an adversarial proceeding with enforceable rules of evidence and procedure, such as an American federal trial court operating under pre-PATRIOT Act standards.
Good morning, Katherine.
Kadlec is referenced here as the boss of Michael Callahan. Michael Callahan is the Spook Doc and Scientist who Dr. Robert Malone has stated tipped him off to the Wuhan virus.
https://siliconicarus.org/2020/07/31/darpas-man-in-wuhan/
"Simultaneously in the U.S., it is claimed, an old colleague of Callahan’s Dr. Robert Malone had been conducting a study with U.S. government-sponsored research teams. Specifically, Malone was working alongside U.S. Defense Threat Reduction Agency (DTRA) consultants to carry out supercomputer-based analyses to identify existing FDA-approved drugs that may be useful against the novel coronavirus responsible for COVID-19. Per their analyses, famotidine turned out to be the “most attractive combination of safety, cost and pharmaceutical characteristics“.
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Sage note: *Note that this computer modeling system, called DOMANE, which Malone worked on somehow managed to spit out Remdesivir as a live trial treatment for COVID-19.
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-------Callahan, who by then had been recruited to be Special Adviser on COVID-19 to the Assistant Secretary of Preparedness and Response (ASPR), Robert Kadlec, was presented the joint findings of the U.S. DTRA and Dr. Malone. Both Dr. Callahan and Malone claimed to be unaware of each other’s conclusions regarding the anti-acid, and despite agreeing to collaborate, each claims to have made the initial discovery. Malone offered a February post on LinkedIn as proof, where he asserts that he was “the first to take the drug to treat my own case” upon discovering the proper dose. Callahan, meanwhile, never provided any evidence of his ostensible breakthrough, though he claims to have told Dr. Malone himself about the discovery before the Virginia-based physician began running the sequences through DTRA computers.
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Master of the Dark Sciences
After a few years bouncing from one former Soviet lab to another, Michael Callahan would return to the United States with a head full of new ideas and a brand new job at the Pentagon’s Defense Advanced Research Projects Agency (DARPA) where he could put it all to use as director of the agency’s biodefense therapeutics portfolio.
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Prophecy was another program created by Callahan at DARPA. It sought to “transform the vaccine and drug development enterprise from observational and reactive to predictive and preemptive” through algorithmic programming techniques. In layman’s terms, the program proposed that “viral mutations and outbreaks” could be predicted in advance to more rapidly counter the unknown disease with preemptive drug and vaccine development.
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Sounds very similar to DOMANE in the sense of trying to get ahead of drug and vaccine development.
Quite a bit of overlap between the nature of Callahan and Malone's work and it makes sense that they would collaborate.
You must wonder the extent of the knowledge that Robert Malone has of what has gone on behind this curious world of DARPA and Michael Callahan.