According to the Freedom of Information Act (FOIA), everyone has the right to access official information from federal authorities. But what is the FIA ββreally worth in practice?
Why can health authorities delay the release of requested documents for years? And why, when the documents are finally released, are they usually redacted beyond recognition, even though complementary information has since become available internationally?
Since February 2022, we, a group of chemistry and physics professors, have been seeking information on mRNA vaccines from our national and European authorities.
We are particularly interested in analytical measurement methods for vaccine quality assurance and tolerances regarding the integrity and concentration of ingredients.
As far as we understand, this information is not subject to the manufacturers’ trade and business secrets, but is provided to them by the authorities. The highest authority responsible for the approval of medicinal products, including in Germany, is the European Medicines Agency (EMA).
According to its own internal rules for dealing with the Freedom of Information Act, EMA allows every EU citizen to request two documents, which must be provided within two years. We requested documents important to the public in April 2022.
NEW – Even after three years of intensive efforts by a group of Chemists in Germany, questions about the quality of the novel mRNA injections have not been answered by the European Medicines Agency. pic.twitter.com/kqHTiiyev8
— Disclose.tv (@disclosetv) April 21, 2025
CDC Releases Paper on Myocarditis After COVID Vaccination, and EVERY WORD Is Redacted
— The Vigilant Fox π¦ (@VigilantFox) March 18, 2024
β148 pages. The entire thing is redacted. What good does a study do if thereβs nothing there?β
Thereβs obviously something very damning that theyβre trying to hide.
Dr. @P_McCulloughMD says⦠pic.twitter.com/1GjI5IKKgB
