Discover more from The Kingston Report
Pfizer Can Be Sued for Toxic and Harmful Substances Found in mRNA Vials
The false claim that Pfizer is not liable for the toxic and harmful substances found in their mRNA vials is unfounded, reckless, and potentially criminal.
April 13, 2023: The false claim that Pfizer is not liable for the toxic and harmful substances found in their mRNA vials is unfounded, reckless, and potentially criminal.
Per their contract with US Army, Pfizer is legally bound to the US laws regulating good manufacturing practices (GMP) for their FDA-approved mRNA ‘vaccines’ and good lab practices (GLP) for human clinical trials and emergency use authorized mRNA ‘vaccines’. This means that all of the substances in Pfizer’s mRNA vials have to be proven to be safe for human use. If any of the ingredients are not safe, Pfizer is liable for the injuries and deaths caused by any chemicals, toxins, or other harmful substances contained in their mRNA vials.
Pfizer’s Operation Warp Speed contract with theUS Army and Department of Defense (DoD) is for the for production of safe and effective mRNA vaccines that protect against SARS-CoV-2 infection and variants. The safety of Pfizer’s mRNA injections (per standard laws of FDA approved biologics) is emphasized several times throughout the contract. This is why Pfizer’s contract also clearly delineates that Pfizer is legally bound to good manufacturing practices and liable for any toxic ingredients in the mRNA vials that results in the disease, disabilities or death of American adults or children. Whether the mRNA ‘vaccines’ are emergency use authorized product or FDA-approved does not matter, Pfizer is liable per the contract.
Contract States Pfizer Must Adhere to FD&C Act Manufacturing Laws
Under the Manufacturing Development Plan of Pfizer’s contract, it specifically states, “…the manufacturing process for the vaccine product to ensure conformity with 501(a)(2)(B) of the Food, Drug and Cosmetics Act (FD&C Act, Title 21 United States Code (USC) regarding good manufacturing practices (GMP).”
Per section 501(a)(2)(B) of the FD&C Act, a drug (or biologic) Pfizer must ensure that they follow good manufacturing practices to ensure that their mRNA injections meet the requirements of safety of any FDA-approved or authorized product for human use.
This means all substances in the vials must be safe for human use. The contract states that, “Pfizer shall scale up its capabilities for….manufacture, analysis, and release of GMP materials (mRNA).”
Analysis means that Pfizer will ensure quality control testing of the final product’s purity and consistency at the manufacturing facilities.
Many experts have proven that there are toxic levels of plasmid DNA, graphene oxide, and other substances harmful to humans found in the mRNA vials, as well as finding no mRNA itself in the vials. These findings are clear violations of Pfizer’s DOD contract and the laws that govern EUA and FDA-approved products.
Claiming Pfizer is Not Subject to FDA Manufacturing or Safety Laws is Extrinsic Fraud
An alleged expert in contracting large clinical trials for pharmaceutical and medical device companies has claimed that all mRNA injections are Emergency Use Authorized (EUA) countermeasures and that they can not constitute a clinical investigation or comply with current Good Manufacturing Practices and US regulatory laws.
These are false and reckless statements from a revered clinical trial contract expert. If used in a court of law, this type of ‘expert’ testimony could quite literally enable Pfizer to get away with murder.
Not only does Pfizer’s DOD contract clearly state that Pfizer will ensure the quality, purity and safety of their mRNA product for both human experimental use and FDA-approved use, but the contract also bounds Pfizer to the 2017 EUA Regulatory Guidance issued by the FDA.
There has been an absurd claim made that FDA clinical trials can not be conducted for a product, if that product is currently being used under Emergency Use Authorization. This claim couldn’t be farther from reality.
The 2017 FDA Guidance on EUA Products states (verbatim), “In fact, human data derived in the course of studies conducted under an IND (initial new drug application clinical trials - phases 1/2/3) may help to support an FDA conclusion that the available evidence is adequate to support an EUA consistent with the statutory criteria.”
This means that the FDA strongly encourages manufacturers to initiate and follow-through on completing standard FDA clinical trials regulated by the FD&C Act while an EUA is in place. To be clear, this does not mean the FDA clinical trials were play theatre.
I’m sorry some admired experts and attorneys have misrepresented important material evidence and the laws regarding Pfizer’s EUA and FDA-approved mRNA injections.
The Kingston Report. TRUTH WINS.
Mathew 23: 27-28
"Woe to you, teachers of the law and Pharisees, you hypocrites! You are like whitewashed tombs, which look beautiful on the outside but on the inside are full of dead men's bones and everything unclean. In the same way, on the outside you appear to people as righteous but on the inside you are full of hypocrisy and wickedness.”
Placing the International Crime of Using of mRNA Technology on Civilians Solely on the US Government and US Military Can Lead to Global Military Intervention, also Known as World War III
The enemies of America are very pleased each time an attorney or expert diverts our attention from taking down Pfizer and instead focuses us on demanding that our own military and government are prosecuted for global war crimes. Are we supposed to wait on outside global military powers to prosecute not only Pfizer, but also the US government, US military and therefore all of the U.S.A.? Am I the only American citizen who sees this as a terribly flawed strategy?
Expertise and Intelligence is Required to Win an Intelligence War
Lieutenant General Krillilov, the Russian Military Chief of Nuclear and Biowarfare, cites my med-legal analysis in his most recent global briefing on Pfizer’s role in the use of mRNA technology bioweapons on civilians under the guise of ‘safe and effective vaccines’ and has launched a global criminal prosecution case against Pfizer. Lieutenant General Krillilov cites my work and affirms that the mRNA vaccines are by definition agents of biowarfare per 18 USC 175.
I’ve been fighting this psychological war to educate Americans and our government officials for two years now. If you want America to take control of this biowarfare nightmare, please reach out to government leaders and powerful media influencers to request for me to present the evidence that can take down Pfizer and stop the mRNA technology platform dead in its tracks. I can be reached through firstname.lastname@example.org.
Keep up the good fight!
People often ask me for advice on supplements and medical treatments. I can’t make medical recommendations for you, but for me, I know that reducing the level of acid in your body and taking a supplement that contains zeolite can help remove toxic metals from your body.
I use TouchStone Essentials Zeolite daily.