THE pharmaceutical industry's main role in the 'pandemic' project has been to provide cover for what is a military bioterrorism programme, it has been claimed.
Sasha Latypova is a former research and pharmaceutical development executive who has supervised more than sixty clinical trials of new drugs for the industry, and understands every step of the regulatory protocols which govern bona fide studies and trials.
In early 2021, however, she observed that the strong safety surveillance signals of the new injectables being registered in the U.S. Vaccine Adverse Events Reporting System (VAERS) were not triggering the automatic stop and recall mechanism, and the relevant regulatory bodies were showing no concern.
This led her to conclude that there was malicious intent.
From then on, she set about examining minutely every aspect of the development, procurement and manufacturing processes of the 'vaccines' being rolled out en masse, through Freedom of Information (FOI) requests.
To illustrate her point, she explains that in January of 2021, an unusual number of allergic reactions were flagged up in California, following administration of the Moderna product. In any normal safety surveillance system, lots are tracked by their numbers, and if a clustering of problems or deaths occurs with certain batches, these are immediately recalled for analysis. This is automatic and is done by the manufacturers, in the same way as for car parts or food products.
Instead, in this instance, the lots in question were simply distributed more widely, causing sixty-five deaths and three thousand serious adverse events. Latypova explains that once a safety signal is flagged up and no recall action is forthcoming, law enforcement is normally triggered and prosecution of those responsible follows.
Diese Geschichte stammt aus der Issue 34: June 2023-Ausgabe von The Light.
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Diese Geschichte stammt aus der Issue 34: June 2023-Ausgabe von The Light.
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