The multi-billionaire Ugur Sahin, who resides with his company at the address in Mainz “An der Goldgrube 12”, announced in a newspaper interview that future changes to his “vaccines” should refrain from human studies.
The article “Biontech boss in alarm mode” appeared in the Wiesbadener Kurier – the online version is available found here (link) but like many publicly relevant topics once again well hidden behind the paywall. We have the print version:
Sahin is demanding nothing less for the approval of vaccine adaptations than the waiver of additional clinical studies on humans, which are actually common…
Meanwhile, the discussion of unwanted side effects, serious side effects, and even fatal side effects has reached the mainstream. Almost every mainstream medium now reports on tragic “individual cases”. Those affected are usually let down by the system, as just talking about it was previously considered taboo. Even the German Health Minister Lauterbach, who doesn’t always seem particularly loud, recently admitted that there were serious side effects (After 1.5 years he finally admitted it: Karl Lauterbach: There are very serious side effects).
However, Sahin does not speak to the Wiesbaden courier about side effects. He speaks of the danger of new variants that could be expected from autumn. On the other hand, one would have to “vaccinate” as soon as possible. The multi-billionaire sharply criticizes the fact that the approval authorities expect proof of the effectiveness and harmlessness of the sprays used. He calls for “rapid approval of adapted vaccines”. According to Sahin, new clinical studies would be unnecessary, since only a few components of the “vaccination” would be changed anyway. Before the Corona crisis, vaccine approval in less than ten years was completely unthinkable.
Incidentally, according to research by Report24, not a single ampoule, let alone a batch of the BioNTech “vaccine” in Austria, has been tested for composition and purity. You rely on Germany. A recent letter from the PEI casts doubt on the fact that much more than a “visual inspection” was carried out there. Because just a few days ago asked the PEI at BioNTechaccording to which criteria one can check the quality of the “vaccines” at all:
Please let us know how and with which control methods the quality of the mRNA is assessed, ie how the identity of the mRNA species, the amount of truncated or faulty mRNA compared to the full mRNA is determined.
This means – and we only came to this conclusion after several months of research – that at least the entire German-speaking area blindly relies on BioNTech’s assurances that the ampoules contain what is claimed. And on this basis one wants to carry out compulsory vaccinations of the population!
