It brings together two experienced pharmaceutical professionals with very different careers in the industry. Their individual knowledge and research shows that both government and industry are not telling the truth about the safety of coronavirus vaccines.
Brian Gerrish and Debi Evans, Alexandra (Sasha) Latipova, Former pharmaceutical industry executive who has it cooperated with many companies Including Pfizer. Brian and Debi will also join us. hedley leasewho kindly facilitated this interview with Sasha.
Sasha Latipova is from Ukraine and has lived in the United States since the 1990s. After founding a number of successful companies focused on clinical trial reviews, she decided to sell the companies and leave to focus on her art.
When the World Health Organization declared: coronavirus pandemic In early 2020, in the wake of an apparently false mistrust of hydroxychloroquine, Sasha said that all the safeguards and good manufacturing practices that we all rely on to deliver us are being followed. It didn't take long for me to start noticing. safe and effective Pharmaceuticals were abandoned in favor of rolling out new experimental “vaccines” using mRNA. She set out to research thousands of papers and vast amounts of data.
After accessing and examining U.S. Department of Defense contracts for coronavirus vaccinations, treatments and diagnostics, Sasha Latipova quickly discovered that Pfizer and Moderna effectively formed a cartel and that their contracts They discovered that it had been treated as a military matter and was therefore exempted from any responsibility. As long as the person concerned complies with the order, PREP methodwhich establishes the framework for America's emergency preparedness.
As many pharmaceutical industry commentators have pointed out in recent years, big pharma brands do little more than marketing these days, leaving the manufacturing of hundreds of basic components of branded products to far more obscure companies. It is left to the complicated nest of companies. In this interview, Sasha Latipova explains how the Department of Defense planned, owned, coordinated, and (her In my opinion, I think I was deceived), but I am explaining how I have managed it. Her no-nonsense explanation and tour of evidence is sure to shock and educate our audience. The mRNA platform will continue to exist and continue to harm and kill those who give their bodies away. Sasha has given candid testimony many times, Submitting evidence to Germany's coronavirus commission.
Her testimony essentially goes like this: The safeguards, checks, and regulations that citizens have relied on to protect themselves from harm have been removed in the name of the coronavirus. Prototypes (defined in the pharmaceutical industry as well as in other industries as a normally working new product or new version of an existing product) for each brand's coronavirus injection were manufactured under the U.S. Department of Defense. prototype contractTherefore, there is no responsibility or requirement for safety or effectiveness.
We learned that different batches of coronavirus shots vary widely in toxicity, and that pharmaceutical companies can't manufacture mRNA platforms in the quantities needed to attack the world. Sasha Latipova's case concludes that manufacturers and drug brands conspired to commit what she calls “regulatory and manufacturing fraud.” If we analyze America, Vaals Database of serious side effects data. It is a much more satisfying tool than the UK MHRA's equivalent database. yellow card datashe realized that no one knew exactly what was being injected into her or how toxic it was. It's a lottery. (UK Column previously interviewed France's Christine Cotton about VAERS data.)
With exemplary fortitude, Sasha speaks to the UK Column about what she discovers through her tireless research, including the risks to pregnant women, breastfeeding mothers and their babies.
Hedley Rees (previously interviewed by UK Column) is a Managing Consultant at PharmaFlow Limited, a UK-based consultancy specializing in operations and supply chain management in the life sciences. He has over 35 years' experience in industrial engineering, logistics and supply chain management, having previously held senior positions at Bayer UK and British Biotech. In this interview, Hedley explains how he discovered that mRNA “vaccines” should never be frozen, and why he didn't.
Safety signals are ignored and the batch is not recalled despite warnings from authorities. In Orange County, California, in 2021, a batch of Moderna's coronavirus vaccine caused an excessive number of severe side effects, resulting in many deaths. The warning caused by this was ignored.
There is so much information buried in this deep ocean of knowledge that this interview is just a taster. Sasha kindly agreed to speak with us again and reveal more details. Thank you, Sasha and Hedley, for shedding light on an area that most of us don't even know exists: how vaccines are created.
Sasha Latipova provided the following text to UK Column along with the interview.
This is the presentation I referenced on the US regulatory agency FDA's website. Just 45 minutes into the interview, vaccine and Recommendations regarding related biological products. Committee October 22, 2020 Meeting Presentation Written by Dr. Robert Johnson Organization chart is on page 12 (Internal numbering, equivalent to p.11 of PDF file page numbering)and page 17 shows a “portfolio,” but it's actually much larger and more versatile than it appears.
for example, Here it is under the umbrella name of Medical CBRN Defense Consortium.all companies, universities, and universities that the U.S. Department of Defense can currently contract under other trade authority within the military consortium for chemical, biological, radiological, and nuclear “countermeasures” (i.e., production of military “prototypes”); and non-profit organizations. (I interpret this as a weapon).
