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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).