The Last Chance Of Freedom : C-19 Injections: Massive Regulatory and Manufacturing Fraud

Saturday, November 26, 2022

Background

Alexandra Latypova is an ex-pharmaceutical industry executive with a lot of experience in the areas of drug safety and clinical trials
Based on the number of reported deaths and adverse events per lot, there was unprecedented variability in the toxicity of the product
According to Alexandra, the mRNA shots do not conform to their label specifications, and "in practice, both 'blank' and 'lethal' vials and anything in between is produced"
Analysis of publicly available data found strong evidence of manufacturing and regulatory fraud

Alexandra grew up in Soviet Ukraine and immigrated to America in the late 1990s.
She received her MBA from Dartmouth College and spent twenty five years in pharmaceutical industry and biotech, and founded a number of successful startups, sold them, and retired, hoping to focus on painting.

Alexandra is one of the team members behind the famous “How Bad Is My Batch” webpage where people can look up the number of severe adverse events reported to VAERS associated with a COVID injection lot number.
The uneven distribution of deaths per a hundred thousand doses from batch to batch in the U.S. showed the worst state is South Dakota (30+ reported deaths per 100,000 doses).
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COVID injections products are garbage soup
Massive non-compliance of the vial content to the specifications
Non-compliance with Good Manufacturing Practice
Vials of mRNA injections are not tested by the manufacturers for conformity to the label
The more they conform to the mRNA specification, the deadlier they seem
It is expressly forbidden by the international vaccine supply contracts to perform vial tests

There is evidence of collusion between the manufacturers, the global regulatory agencies, and the US Department of Defense
This led to the commercial release of the Covid-19 countermeasures that do not comply with the current Good Manufacturing Practices (cGMP)
Evidence includes Moderna's non-clinical study summaries, Pfizer's Chemistry Manufacturing and Controls documentation, and contracts between pharma and the DOD for supply of the mRNA/DNA products

The company submitted 700 pages of documents to the FDA, but of these, 400 pages are irrelevant studies that Moderna repeated multiple times.
Moderna also submitted three versions of a single module, and one module contained only narrative summaries of Moderna's studies, but no actual study results.
The FDA did not object to any of this.

The manufacturer and the FDA conspired to push an entirely novel technology and product on millions of people without carrying out a single well designed safety assessment
4 different variants of active ingredient were included in the single Investigational New Drug application by Pfizer
Each chemical or biological entity is nevertheless deemed legally distinct for the purpose of product approval
Pfizer's program did not include a comprehensive end-to-end test of all components of the final approved product (the mRNA COVID-19 vaccine).

But We Are Not Helpless
The challenge is centuries old, and remembering it can bring us much needed perspective and balance.
Throughout history, many of our ancestors had to deal with tyrants, and today, it is our turn to be brave. May our brave ancestors be our inspiration.

The Last Chance Of Freedom