Do C-19 Vax Manufacturers Violate cGxP?

Master class in pharmaceutical regulations: the difference between EAU and EUA that nobody on Earth has noticed in the past 3 years. Including me until yesterday afternoon.

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Let’s look at the clip of recent JJ Couey’s debunking the Debunk guy debunking Kevin McKernan. I hope you can keep track of all the debunking. All of this centers around the CHD video “Intent to Deceive” where Kevin discussed his finding the SV40 promoter sequence in Pfizer’s vials and the fact that someone inside Pfizer or inside its contractor or ultimately at the DOD (where all contracts originate) went into trouble of deleting that sequence so it does not show up in the documents that Pfizer submitted to the regulators like FDA, EMA, TGA, etc. So there was an intent to deceive the regulators, vaccinators and the public about the presence of this well-known nuclear localizing, cancer-inducing piece of code in the injections. You can watch JJ Couey’s full twitch stream here.

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Well, JJ Couey is not really debunking the Debunk guy, but rather using his line of argument to criticize Kevin and CHD. Both positions here are not correct IMO. Let’s review.

The Debunk Bro is easy - he is a paid propagandist and simply repeats the FDA/CDC/HHS/DOD prescribed narrative. The narrative goes like this:

• Kevin got vials from who knows where, we don’t know if they came from Pfizer and Moderna or maybe they are fake!

• Lengthy discussion of existing cGxP laws - every pharmaceutical must be in compliance, look at all the quality checks, and tests and quality control procedures that must be in place before approval, then all the batch-release testing for each batch, so many rules everyone must comply, yada, yada, therefore what Kevin says he found in the vials cannot happen! Because cGxP.

JJ Couey’s position can be condensed to the following:

• Because cGxP, FDA will use the “contamination” finding to remove the product from the market and maybe superficially punish Pfizer.

• The mRNA poison will be cleaned up from SV40 and DNA plasmids and put it back on the market and continue.

• The mRNA is poison with or without SV40, because it is transfecting cells and nothing positive to health can happen that way. Only damage can result from this.

That last bullet I 100% agree with, and I don’t believe Kevin McKernan or anyone involved in the vial testing activities disagrees with it either.

What’s wrong about both positions - the highlighted part. Both rely on the assumption that covid jabs are pharmaceutical products subject to cGxP laws and FDA regulations, and therefore finding and proving a cGxP violation may result in recall or another pharmaceutical law enforcement action. That’s the most profound lie on which this whole situation hinges. I am not at all surprised that the Debunk Bro promotes this lie (he is paid to do so), but I am more concerned that JJ Couey seems to be thinking that way, too.

Covid-19 poison marketed as “vaccine” is NOT a pharmaceutical product subject to cGxP laws and FDA enforcement powers under 21CFR 312.

Let’s recall:

21 USC 360bbb-3(k): use of EUA-covered medical countermeasure (MCM) products, once designated as such by the Secretary of Health and Human Services “shall not be considered to constitute a clinical investigation.” 

The definition of clinical investigation from cGxP (21CFR part 312):

Clinical investigation means any experiment in which a drug is administered or dispensed to, or used involving one or more human subjects. For the purposes of this part, an experiment is any use of a drug except for the use of a marketed drug in the course of medical practice.

There are 3 mutually exclusive categories of pharmaceuticals regulated by cGxP laws:

• FDA approved/marketed;

• In clinical trials under IND exemption;

• “Expanded Access Use” products (EAU, colloquially referred to as “emergency use” or “EUA”)

There is a 4th category of things imagined and fabricated more recently (after 9/11) that is mutually exclusive with these 3 categories above, by way of legal magic and word confusion:

• EUA Countermeasure under Public Health Emergency which is regulated (sort of, but mostly just waved through with lots of panic and confusion) under para 564 of the Food, Drug and Cosmetics Act.

This “EUA” is not the same “EAU” (are you following this?) as it requires the situation of total global panic because of a few false-positive PCR tests primed with some code from a post-it note and about 40 Chinese murdered in Wuhan with remdesivir and ventilators under supervision of you know who. EUA exists when PHE and PREP Act declaration are in force:

Relevant post by

Bailiwick News

with more details about legal status of Countermeasures here.

Here is a slide from “Legal Preparedness” deck of the FDA from August 2020, discussing the same concept. EUA (no IND) is not EAU (which requires IND). In the same presentation the FDA lawyers state that “certain [pandemic] preparedness activities [without EUA + PREP Act shield] would otherwise violate the FD&C Act”. “Legal preparedness” is exactly what it sounds - they write new illegal-laws that allow them to break all established laws. They fully plan to poison people and anticipate massive numbers of injured plaintiffs. And they know that they need to build many walls of their legal fortress so that no actual justice can occur.

Credit to David Wiseman for fishing out this absolute gem from a 400 page transcript of the VRBPAC meeting on October 22, 2020. Here Doran Fink (then at FDA, currently enjoying his reward for the job well done at Moderna) explains why EUA and not EAU regulatory pathway was used for Poison-19 injections. Annotations and emphasis are mine:

P201/408 of transcript:

“DR. KURILLA: And then for Doran [FINK], did you consider at all the possibility of an expanded access protocol for those specific groups that you would issue the indication for the EUA instead of an EUA? [notice they are themselves confused between EAU and EUA!]

P203 Dr. FINK: Yeah. So to answer your question about an expanded access protocol [EAU or Expanded Access], that is another regulatory mechanism for providing access to investigational vaccine. I think if we were to consider an expanded access protocol of the same size and scope as what is being considered for an Emergency Use Authorization, then the benefit/risk considerations and the data to inform those benefit/risk considerations and allow that type of use would be highly similar. The differences between expanded access use and Emergency Use Authorization are that expanded access use is done -- or is carried out under FDA's investigational new drug regulations. So among many other things, those regulations require use of an institutional review board and also obtaining informed consent from recipients of the investigational vaccine according to regulations for clinical investigations -- research use of investigational vaccines. And so operationally speaking, an expanded access protocol would add some complexity, and that is why Emergency Use Authorization is being considered primarily as the mechanism for addressing the public health emergency that has been declared.”

I think it’s time to put the issues of the informed consent and the need to follow cGxP regs to rest, isn’t it? The FDA officials clearly explained here that the reason they went with EUA is specifically NOT to follow any investigational drug rules or cGxP, and NOT to provide informed consent. And it is legal for them to do so for EUA under PHE!

This explains many many things, but still does not explain the curious Schroedinger cat-like phenomenon of both EUA and the FDA’s assertion of “full approval” co-existing for covid poisons, unless of course we realize that the “approval” is a fake. There cannot be an FDA approval per 21 CFR 312 if IND and clinical trials are not relevant to it.

From the same FDA lawyer presentation, observe the process of issuing EUA:

This process consists entirely of “determinations” (opinions of a bunch of bureaucrats) and declarations that “circumstances exist”. Did you see a box on this chart that said “open IND and complete a clinical trial, it’s ok to do it badly and break a bunch of rules, but you still need to do it”? Was there any box saying “safety/efficacy data review”? No? I don’t see those either. Clinical trials were IMMATERIAL. Judge Truncale said so when dismissing Brook Jackson’s case under allegations of serious fraud.

Let’s not forget, that an extra precaution of PREP Act must be in place for this scheme of conducting illegal experiments without informed consent can take place. It is in fact so critical that it is prominently specified in the Emergent Biosolutions-DOD contract for manufacturing Poison-19 injections (they were the manufacturer of AstraZeneca and Janssen poisons):

On page 49, you can read :

"In the event the Contractor delivers vaccine under this contract which is not covered by the aforementioned declaration (PREP ACT) because of the expiration of the aforementioned declaration (PREP ACT) and any renewals or amendments thereof, the Government agrees that the medical countermeasure delivered by the Contractor under this contract will not be administered for use in humans."

They are fully aware that without the PREP Act the Medical Countermeasures cannot be used in humans. None of the real pharmaceutical products have this requirement.

Do fentanyl dealers violate cGxP? Rhetorical question.

If a substance cannot be subject to clinical investigation, the Investigational New Drug (IND) exemption for it is meaningless, and so are the clinical trials, and review and approval in compliance with cGxP. The best part of this: if you cannot really comply with cGxP, violations of cGxP cannot happen either!

Here is the thing about SV40 finding, it’s not the only evidence of contamination, adulteration or violation of cGxP for these products. I can list perhaps hundreds of examples of severe violations of cGxP, many I have reported on since 2021, and many that were documented by dozens of people worldwide. Clear and undeniable violations of all laws that relate to consumer safety and pharmacy distribution in the US and other countries. That’s because NONE of them apply to “EUA Countermeasure under PHE”.

Can cGxP violation/contamination argument still be used to remove this poison from the market?

This theoretical possibility of this remains, as hope is the last one to die on this planet. However, I am pretty certain at this point that the FDA has dug themselves into a very deep hole via rigorously not noticing any severe cGxP violations that continue to exist in reality over the past 2-3 years. They use capricious methods to occasionally “notice” things that help them solidify their ability to further engage in this crime by creating useful case law - such as the case of them “noticing” glass shards in remdesivir and allowing the one injury lawsuit to proceed which will simply help the HHS/DOD to defend PREP Act legitimacy in the future. “See, the injured do have recourse! We regulate quality and cGxP applies!”

With SV40 it is not as simple as glass shards. The SV40 issue is much hotter for them as they cannot really acknowledge it as a problem without opening a larger can of worms pointing to premeditated mass poisoning, and lying about fake-“approving” this stuff to fool the public and especially to fool the professionals.

Let’s recall the DOD-lead Operation Warp Speed and BARDA’s own slides explaining how these stable geniuses were never planning to comply with cGxP in the first place (yellow box is my annotation):

The Debunk Bro is simply spewing the prescribed narrative of the criminal FDA-DOD-Pharma cartel describing all the regulations that exist (cGxP) “forgetting” to mention that they do not apply to the “EUA Countermeasures under PHE”. In fairness, he probably doesn’t know this, and that makes him sound more assured and convincing as a paid actor that he is.

Once the status of these illicit substances is understood, it is easy to debunk the Debunk Bro. They are illicit poisons which are trafficked the same way fentanyl or heroin are trafficked world wide (and probably by the same main actors). Kevin’s work is extremely important to stopping these shots by educating the public world wide, and energizing the few legislators with remaining conscience. That is not to diminish the point that even in the “uncontaminated” form, the mRNA platform is a very dangerous poison and should not be used for any application.

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Art for today: Portrait sketch, oil on panel, 12x16 in.