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On the Front Lines: What’s in That Vial? You Will Never Know

Whether or not you want to believe it, the U.S. Department of Defense (DoD) has managed the Covid response in its entirety. The vaccination biowarfare and tyranny we have experienced over the past three years have been pure theatre — or, in other words, a very sick show. The DoD was, quite simply, running a war effort in which Americans were manipulated, deceived and coerced concerning the virus origins and vaccine mandates. “Safe and effective’” proved to be neither.

The manufacturers of the vaccines, who were contracted by and reporting to the DoD, knew absolutely that these injections were anything but safe or effective. It should surprise no one that Pfizer wanted to bury the clinical trial data for 75 years.

So if the DoD was pushing these shots and covering for pharmaceutical companies, why is it that virtually no one knows what’s in these Covid vaccine vials? Sasha Latypova, a pharma/regulatory clinical trials professional turned independent investigator, wrote an extensively researched Substack article titled “Nobody Knows What Is in the Vials.” She states, “Covid-19 injections are dangerous, non-compliant biological materials. Their production must be stopped until a full investigation can be done.”

The mRNA injections in no way conform to their label specifications. Latypova indicates, “Vials of mRNA injections are not routinely tested by the manufacturers for conformity to the label.” Lack of testing prompts Latypova to ask, “How is the public assured that each Pfizer dose contains 30 mcg of mRNA as stated on the label? What level of variability of [mRNA] and other ingredients is acceptable?” Latypova writes, “The mRNA shots do not conform to their label specifications. In practice both ‘blank’ and ‘lethal’ vials and anything in between is produced. Without full compliance, nobody, not even manufacturers or regulators, know exactly what ends up being produced.”

According to Latypova, “The only vial-level tests specified by Pfizer in leaked Chemistry Manufacturing and Controls (CMC) documents are the vial weight at filling, manual inspection for large visible particles and some tests related to integrity, such as vial capping.” That’s it. Basically, hold it up and look at it. Incredible, in the truest sense of that word.

Latypova studied the contracts Pfizer had with the U.S. government. As per the contracts, the product is shipped to the DoD, which retains 100 percent control and ownership of the vials until their contents are injected into people. She did not find any documentation on a sampling of the vials for the purpose of verification of their contents vs. the label. And the contracts specify that “it is expressly forbidden by the international vaccine supply contracts to perform the vial tests for label conformity.”

Despite the distressing ban on third-party, independent vial testing, there has been covert random testing of the vials happening worldwide. Latypova discovered that thousands of vials were “obtained and tested by dozens of research groups working independently of each other.” The consistent findings of all these groups are that they have yet to find one single vial “in full conformance to the manufacturer’s label.”

According to Latypova, a “high-quality report summarizes experiences testing vials from various manufacturers in Germany.” The report found that “some vials contain RNA as well as high concentrations of DNA and protein impurities in quantities far exceeding allowed limits specified by the manufacturer.” In other instances, vials are found not to contain any RNA or DNA. In other words, there are “blank” vials.

In addition, Latypova reported, “Almost all vials examined contain high contamination levels of various metals that are toxic to [the] human body. This finding is consistent across all groups and methodologies, and therefore should be deemed more conclusive.”

Other substances found include “various forms of carbon, including, potentially graphene oxide, … a known toxin.” Almost all vials examined contain a toxic soup of “nano- and micro-particulate contaminants,” of which there is much “photo and video documentation.” These images are frightening and cannot yet be explained. The contaminants are bizarre objects, and some vials are “teeming with them.”

Latypova’s conclusion “is that the products are extremely ‘dirty,’ do not conform to their labels and should thus be deemed adulterated. This is a clear indicator that the manufacture of these products is not compliant” with the Food and Drug Administration’s official “Good Manufacturing Practices.”

Whether or not you want to believe it, the U.S. Department of Defense (DoD) has managed the Covid response in its entirety. The vaccination biowarfare and tyranny we have experienced over the past three years have been pure theatre — or, in other words, a very sick show. The DoD was, quite simply, running a war effort in which Americans were manipulated, deceived and coerced concerning the virus origins and vaccine mandates. “Safe and effective’” proved to be neither.

The manufacturers of the vaccines, who were contracted by and reporting to the DoD, knew absolutely that these injections were anything but safe or effective. It should surprise no one that Pfizer wanted to bury the clinical trial data for 75 years.

So if the DoD was pushing these shots and covering for pharmaceutical companies, why is it that virtually no one knows what’s in these Covid vaccine vials? Sasha Latypova, a pharma/regulatory clinical trials professional turned independent investigator, wrote an extensively researched Substack article titled “Nobody Knows What Is in the Vials.” She states, “Covid-19 injections are dangerous, non-compliant biological materials. Their production must be stopped until a full investigation can be done.”

The mRNA injections in no way conform to their label specifications. Latypova indicates, “Vials of mRNA injections are not routinely tested by the manufacturers for conformity to the label.” Lack of testing prompts Latypova to ask, “How is the public assured that each Pfizer dose contains 30 mcg of mRNA as stated on the label? What level of variability of [mRNA] and other ingredients is acceptable?” Latypova writes, “The mRNA shots do not conform to their label specifications. In practice both ‘blank’ and ‘lethal’ vials and anything in between is produced. Without full compliance, nobody, not even manufacturers or regulators, know exactly what ends up being produced.”

According to Latypova, “The only vial-level tests specified by Pfizer in leaked Chemistry Manufacturing and Controls (CMC) documents are the vial weight at filling, manual inspection for large visible particles and some tests related to integrity, such as vial capping.” That’s it. Basically, hold it up and look at it. Incredible, in the truest sense of that word.

Latypova studied the contracts Pfizer had with the U.S. government. As per the contracts, the product is shipped to the DoD, which retains 100 percent control and ownership of the vials until their contents are injected into people. She did not find any documentation on a sampling of the vials for the purpose of verification of their contents vs. the label. And the contracts specify that “it is expressly forbidden by the international vaccine supply contracts to perform the vial tests for label conformity.”

Despite the distressing ban on third-party, independent vial testing, there has been covert random testing of the vials happening worldwide. Latypova discovered that thousands of vials were “obtained and tested by dozens of research groups working independently of each other.” The consistent findings of all these groups are that they have yet to find one single vial “in full conformance to the manufacturer’s label.”

According to Latypova, a “high-quality report summarizes experiences testing vials from various manufacturers in Germany.” The report found that “some vials contain RNA as well as high concentrations of DNA and protein impurities in quantities far exceeding allowed limits specified by the manufacturer.” In other instances, vials are found not to contain any RNA or DNA. In other words, there are “blank” vials.

In addition, Latypova reported, “Almost all vials examined contain high contamination levels of various metals that are toxic to [the] human body. This finding is consistent across all groups and methodologies, and therefore should be deemed more conclusive.”

Other substances found include “various forms of carbon, including, potentially graphene oxide, … a known toxin.” Almost all vials examined contain a toxic soup of “nano- and micro-particulate contaminants,” of which there is much “photo and video documentation.” These images are frightening and cannot yet be explained. The contaminants are bizarre objects, and some vials are “teeming with them.”

Latypova’s conclusion “is that the products are extremely ‘dirty,’ do not conform to their labels and should thus be deemed adulterated. This is a clear indicator that the manufacture of these products is not compliant” with the Food and Drug Administration’s official “Good Manufacturing Practices.”

What, then, was the main motivation behind this toxic bioweapon?

The obvious answer might be the massive sums of money made available to pharmaceutical companies and others with no legal risk, no regulatory oversight and no accountability for safety and quality. It certainly seems to be negligence, incompetence or a gigantic fraud.

Note that the DoD “contracted Pfizer in May of 2020 for production of at least 100 million doses by October 31, 2020, and up to 500 million doses later. Pfizer’s initial contract award was for $10 billion, with many additional incentives for delivering more doses faster. Similar contracts were made with numerous other ‘vaccine’ manufacturers, and hundreds of other suppliers,” as reported by Latypova.

As the saying goes, follow the (colossal sums of) money. No accountability was built into those contracts for product quality, safety or consistency; in fact, the manufacturers were exempt from all liability under the PREP Act. The DoD, which is the purchaser and distributor, is not properly licensed and accountable as a pharmaceutical distributor. As a result, the product is not serialized and is thus open to adulteration, falsification or mislabeling. There is simply no oversight whatsoever. What could possibly go wrong?

What should be done at this point?

I find myself speechless. The VAERS passive reporting system set up by the CDC currently reports 34,469 vaccine-reported deaths and 1,494,382 adverse event reports dated December 30, 2022 (see openvaers.com). This is more deaths and adverse events than in the last 30 years. And this is information from a self-reporting, passive system.

To me, it looks as if terrible, unholy acts have been committed against people — for good intentions or ill, but certainly for profit.

Katherine Strange is an entrepreneurial leader with more than 25 years of experience managing cross-functional teams and operating a successful business. Her passions include fighting for freedom and finding the truth.

What, then, was the main motivation behind this toxic bioweapon?

The obvious answer might be the massive sums of money made available to pharmaceutical companies and others with no legal risk, no regulatory oversight and no accountability for safety and quality. It certainly seems to be negligence, incompetence or a gigantic fraud.

Note that the DoD “contracted Pfizer in May of 2020 for production of at least 100 million doses by October 31, 2020, and up to 500 million doses later. Pfizer’s initial contract award was for $10 billion, with many additional incentives for delivering more doses faster. Similar contracts were made with numerous other ‘vaccine’ manufacturers, and hundreds of other suppliers,” as reported by Latypova.

As the saying goes, follow the (colossal sums of) money. No accountability was built into those contracts for product quality, safety or consistency; in fact, the manufacturers were exempt from all liability under the PREP Act. The DoD, which is the purchaser and distributor, is not properly licensed and accountable as a pharmaceutical distributor. As a result, the product is not serialized and is thus open to adulteration, falsification or mislabeling. There is simply no oversight whatsoever. What could possibly go wrong?

What should be done at this point?

I find myself speechless. The VAERS passive reporting system set up by the CDC currently reports 34,469 vaccine-reported deaths and 1,494,382 adverse event reports dated December 30, 2022 (see openvaers.com). This is more deaths and adverse events than in the last 30 years. And this is information from a self-reporting, passive system.

To me, it looks as if terrible, unholy acts have been committed against people — for good intentions or ill, but certainly for profit.

Katherine Strange is an entrepreneurial leader with more than 25 years of experience managing cross-functional teams and operating a successful business. Her passions include fighting for freedom and finding the truth.

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