by Rhoda Wilson, Daily Expose:
“[Pfizer] did not defraud the government. We delivered the fraud that the government ordered.” Sasha Latypova used these words to describe the basis on which Pfizer has requested the dismissal of a False Claims Act case brought against them for their covid “vaccines.”
The US Department of Defence ordered “demonstrations” from pharmaceutical companies using the same secretive framework they use to order weapons. While telling us they were pharmaceutical products, for legal reasons they described them as emergency use authorised “countermeasures.” No pharmaceutical regulation applies to countermeasures.
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“They were claiming that they’re producing pharmaceutical products to the good manufacturing standards when they perfectly well knew, I assure you, they were all aware of this. They perfectly well knew that no pharmaceutical regulations apply to these things, countermeasures … They’re just lying to you that these are pharmaceuticals. They’re actually not,” Latypova explained.
The international conference ‘Pandemic Strategies: Lessons and Consequences’ held at the Stockholm Waterfront on 21-22 January 2023 gathered 15 leading doctors, researchers and lawyers from the US, Canada, UK, Germany, France, Belgium, Switzerland, Israel, Ukraine and Norway, along with 7 Swedes.
Presentations and panel discussions are being released in the order that they appeared on the program at a rate of 3 per day.
Alexandra “Sasha” Latypova was one of those who gave a presentation. She holds an MBA degree and is a former Pharmaceutical R&D Executive. Latypova has spent approximately 25 years in the pharmaceutical industry and has owned and managed several contract research organisations – conducting clinical trials for over 60 pharmaceutical clients worldwide. She became concerned about the irregularities, cover-up and apparent fraud relating to the extremely high number of deaths and injuries associated with the covid injection rollout.
In her presentation, she explained that her initial investigation was to look into the so-called covid vaccines’ compliance with good manufacturing practices. It is the practice required to conform to quality guidelines recommended by regulatory agencies and applies to drugs, food and other mass-produced products that are consumed. It is to ensure, for example, that if you buy your favourite beer today and then you go to the to buy it again a week from now or a month from now, your experience is the same. The same goes for medicines like Aspirin that you buy in a pharmacy. You don’t expect a product to be a thousand times different a week from now versus today.
“As a highly regulated industry, pharmaceutical manufacturers are supposed to comply with [good manufacturing practice]. And this means that the product that they claim that they make, with the ingredients that they claim that they make, is supposed to be in every vial, every shot, every pill, over and over and over again, and they should be almost identical to each other,” Latypova said.
In the first few months of her investigation, Latypova found evidence of “very bad manufacturing practices” in relation to the mRNA injections. “When I looked at the [ ] graph [of serious adverse events and deaths recorded in VAERS] for mRNA injections for the US, I found [the below]”
“[I’m] only looking at serious adverse events and deaths. There were almost no adverse events reported in some lots, and some lots had thousands and they had hundreds of deaths. And so, this is not good manufacturing practice-compliant product at all,” said Latypova. “I’m not endorsing flu vaccines or any vaccines anymore, because until this is investigated fully, nobody should be taking anything. That’s my professional opinion.”
The above graph shows Johnson & Johnson (Janssen), Moderna and Pfizer. Below is a graph for Moderna. The blue colour represents serious adverse events and the orange represents death post-vaccination. “A well-manufactured product should not look like this at all,” Latypova explained.
Explaining the significance of the lot labelled in the graph above, Latypova said:
“On January 18, Orange County, California Health Department flagged this particular lot of Moderna for what they called ‘excessive number of allergic reactions’. Nothing was done about it. The injections were not stopped. In fact, this lot was being sold all over the United States until it ran out in late March.
“And as you know, if there is salmonella in a salad, they will recall the entire product from all the shelves in the country. Right? That’s what you should do as a manufacturer. All manufacturers have systems to detect this. And the majority of recalls of products are voluntary because they don’t want this to happen.
“Yet [with this lot from Moderna], nobody stopped. Not the manufacturer, not the health authorities of Orange County, not the CDC, FDA, or whoever was supposed to monitor this, they continued selling this lot. It’s now associated with over 65 deaths in the US and over 3000 serious adverse events. So, after something like this happens, everything that follows is intentional.”
Every researcher that has questioned or challenged regulatory authorities has been told: “We looked at it. It’s safe and effective. Go get vaccinated.” Why were they all behaving this way? Why are they all following the same script the world over?
Latypova has been collaborating with legal researcher Katherine Watt, who publishes articles on a Substack page titled ‘Bailiwick News’, to reveal the legal structure – or rather the pseudo-legal structure as it’s not lawful – of this government, pharma, military criminal cartel. “It actually is operating all over the world,” Latypova said.