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Leaked Emails from EMA Revisited
In late 2020 a collection of documents – approximately 900 pages from Pfizer’s “vaccine” Chemistry Manufacturing and Controls (CMC) section of the regulatory submission to the European Medicines Agency (EMA) were leaked and sent to a number of journalists. The documents also included email exchanges from some of the reviewers and senior executives at the EMA. The leak was covered in the British Medical Journal who were able to confirm that the documents were authentic. I received these documents from a colleague about a year later, at the end of 2021, and I read and used a lot of them in my analyses. I have seen many R&D related documents from Pfizer in my professional work, so I can also confirm that these leaked ones were highly consistent with typical Pfizer documentation. The EMA did not deny the authenticity, and only stated that the headers of some of the emails were changed.
I have a much larger number of followers now and a much clearer understanding of the organization and pseudo-legal structure of the criminal cartel driving the global atrocity colloquially known as the “covid pandemic response”. I am revisiting the leaked emails as I believe that they provide some highly significant evidence.
The EMA email files that I have read contain 14 screenshots of emails from mid to late November 2020. The exchanges are from the EMA staff and senior executives. In my opinion these emails demonstrate that:
- The EMA reviewers were under a massive political pressure to invent new ways of approving the unapprovable dangerous products. The pressure was emanating from the very top of the US, UK and EU governments.
- EU Commissioner, Ursula vonden Leyen made promises to the Member States she was never intending to fulfill in order to tie them all in a single pact for vaccine contracts and thus pre-empt any independent decisions in their own countries.
- There were severe and unresolvable – given the purposefully unrealistic timeline – issues with quality of the product the EMA staff were pressured to ok. Some were uncomfortable with doing so and voicing their concerns. Others “overlooked” clearly made-up data.
Ultimately, the regulatory review itself and the concerns raised did not matter – the product was going to be marketed regardless. We now know exactly why – the regulatory authorities did not have the regulatory power over it. The pharmaceutical regulators do not oversee military materials known as “countermeasures” and “manufacturing demonstrations” (coy language covering up the biowarfare agents made by the captured US Government and its global partners). The emails show that the majority of the EMA staff were unwitting actors in this play.
Confirmation of this for the UK came out recently.
Based on the response to MHRA FOIA:
“All the Covid vaccines and therapeutics authorisation decisions were taken by the Licensing Minister and were not delegated.”
Translation – normally the authority to review and approve new pharmaceuticals is formally delegated to the MHRA from the Secretary of State for Health (UK). In case of covid products, the delegation of authority does not exist. It appears that all of them were deployed singlehandedly by Matt Hancock (although he is pointing finger at someone higher up). The same thing happened in the US – Alex Azar under Trump Administration deployed these noncompliant biomaterials on Americans, and Xavier Becerra under Biden continues to do so today.
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