Liquid evil – the contents of CoVID-19 vials
Criminal negligence or intent – design or manufacture?
Once again demonstrating its presence as “the tip of the spear” in attacking the roll-out of toxic injections, The Expose-UK thrusts that tip into the heart of the reincarnated Fourth Reich of the WEF/WHO/National Health Regulators/Big Pharma criminal racket.
Please donate, I have. They are doing God’s work to prevent the spread of malice and evil.
From here:
https://expose-news.com/2022/09/10/uk-lab-report-graphene-covid-vaccines/
In summary, a forensic report has been present to the UK Police that provides evidence of toxic “inclusions” in four vials – two from Moderna, one from Astra Zeneca and one fro Pfizer. The inclusions are:
The Identified inclusions are:
1. Graphene nano ribbons coated with Polyethylene Glycol
2. Graphene Composite Form 1.
3. Graphene Composite Form 2.
4. Microcrystalline Calcite with Carbonaceous inclusions.
5. Graphene Nano Form with and without fluorescence
6. Graphene nano objects
7. Graphene nano scrolls
The full forensic report is here:
Case Briefing Document.docx (ukcitizen2021.org) (not secure)
ukcitizen2021.org/Case_Briefing_Document_and_lab_report_Ref_AUC_101_Report%20.pdf
It has the following heading:
Case Briefing Document
Offences ● Corporate Manslaughter ● Gross Criminal Manslaughter
Immediate action required: Halt the roll-out of experimental treatments known as “COVID-19 Vaccines” immediately pending Police forensic examinatio
Defendants identified ● AstraZeneca ● Pfizer ● Moderna ● National Health Service (NHS) ● Medicines & Healthcare products Regulatory Agency (MHRA) ● Joint Committee on Vaccination and Immunisation (JCVI) ● Her Majesty’s Government
The evidence has been presented for verification by the multi-million-dollar forensic facilities available to the Police.
Enquiring minds want to know why a private company has had to do this forensic work in the UK and it is not being done by police and prosecutorial bodies In each country where deaths and sever injuries have been inflicted by the injections of these CoVID-19 toxins.
Enquiring minds want to know IF, since toxins have also been discovered in the Astra Zeneca vials, are they ALSO PRESENT IN THE ENTRIE “VACCINE” INDUSTRY IN EVERY VIAL FOR EVERY INJECTION OF EVERY “JAB” (or “SHOT”).
As a reminder, using an Under-Reporting Factor (URF) of 40 (just one event reported to national injection adverse event reporting systems for every forty events suffered), applying this URF to the VAERS and EUDRA reporting systems of the US and EU, then scaling for the one eighth share that EU+US doses make up of 12.6 billion doses administered globally, there may have been 20 million murders and almost 2 billion wounds to internal organs around the world, since the injections began to be rolled out in early December 2020.
Note: BEFORE injection roll-out – 70 million “cases” and 1.7 million deaths globally, using the faulty RT-PCR test as a diagnostic tool at 35-40 amplification cycles (instead of lower than 24).
21 months and 12.6 billion global doses administered later – 613 million “cases” and 6.5 million deaths.
Cases have increased by more than 8 times and deaths by a factor of almost 4. The claim made in clinical trials that the annual case rate (70 million in 2020) would be reduced by over 90%. Instead they have increased by 875%.
Welcome to Planet Stupid – exploited by the reincarnated Fourth Reich.
There is a plethora of information on the toxic ingredients that have NOT been disclosed in the vials. IS this a flaw in the manufacturing process of the toxins, or the vials? Is it isolated to some manufacturing planets or to all manufacturing plants?
For those interested in a fast precis of the graphene “case”, check this out:
Time for the truth on the presence of graphene in the shots – Explore EVERY angle (pennybutler.com)
https://pennybutler.com/graphene-c19-vaccines/
As a reminder, from my previous substack:
Covid19 remedies - the legal ones - by Peter Halligan (substack.com)
21 U.S. Code § 351 - Adulterated drugs and devices | U.S. Code | US Law | LII / Legal Information Institute (cornell.edu)
21 U.S. Code § 360d - Performance standards | U.S. Code | US Law | LII / Legal Information Institute (cornell.edu)
Definition: device from 21 USC § 321(h)(1) | LII / Legal Information Institute (cornell.edu)
Here are the section headings from Code 351
“A drug or device shall be deemed to be adulterated—
(a)Poisonous, insanitary, etc., ingredients; adequate controls in manufacture
(b)Strength, quality, or purity differing from official compendium
(c)Misrepresentation of strength, etc., where drug is unrecognized in compendium
(d)Mixture with or substitution of another substance
(e)Devices not in conformity with performance standards
(f)Certain class III devices
(g)Banned devices
(h)Manufacture, packing, storage, or installation of device not in conformity with applicable requirements or conditions
(i)Failure to comply with requirements under which device was exempted for investigational use
(j)Delayed, denied, or limited inspection; refusal to permit entry or inspection
How Bad is my Batch website (How Bad is my Batch ?) provides a wealth of evidence of poor quality and/or manufacturing practices.
Now the next one that applies to Class 2 devices and some Class 3:
21 U.S. Code § 360d - Performance standards | U.S. Code | US Law | LII / Legal Information Institute (cornell.edu)
(a)Reasonable assurance of safe and effective performance; periodic evaluation
(b)Establishment of a standard
(c)Recognition of standard
(d)Pilot accreditation scheme for conformity assessment
There is a lot more detail within each of these section headings.
Onwards!!!!
https://principia-scientific.com/why-health-officials-wont-let-independent-scientists-examine-mrna-vax-vials/
"“Of particular concern is RNA instability, one of the most important variables relevant to all mRNA vaccines that has thus far received scant attention in the clinical community. …
“RNA instability is one of the biggest hurdles for researchers developing nucleic acid based vaccines. It is the primary reason for the technology’s stringent cold chain requirements and has been addressed by encapsulating the mRNA in lipid nanoparticles.
“‘The complete, intact mRNA molecule is essential to its potency as a vaccine,’ professor of biopharmaceutics Daan J.A. Crommelin and colleagues wrote in a review article in The Journal of Pharmaceutical Sciences late last year.
“‘Even a minor degradation reaction, anywhere along a mRNA strand, can severely slow or stop proper translation performance of that strand and thus result in the incomplete expression of the target antigen.’”
..
“There were considerably more of these fragmented forms of RNA found in the commercially manufactured products than in the products used in clinical trials. The latter were produced via a much more tightly controlled manufacturing process. …
“While we are not asserting that non-spike proteins generated from fragmented RNA would be misfolded or otherwise pathological, we believe they would at least contribute to the cellular stress that promotes prion-associated conformational changes in the spike protein that is present.”
skip to 30 minutes
mercury in multi-dose vials - ask fro single vials
also aluminium
https://live.childrenshealthdefense.org/shows/chd-friday-roundtable
‘Friday Roundtable’ Episode 25: Novavax Deception – What You Need To Know