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FREEDOM OF INFORMATION ACT
A CALL TO OUR HEALTH AGENCIES, GOVERNING BODIES OF THE EUROPEAN UNION AND ITALY:
There is an Urgent Need for Complete Transparency Regarding the Serious Dangers of the mRNA products in use
Governing Bodies, Health Authorities and Agencies by definition and by law exist to serve and protect public health. One key responsibility of these agencies is to ensure the proper evaluation and scrutiny of any new medicines before their authorization and approval for general use. This is particularly necessary with entirely new substances and technologies, such as the recently introduced gene-based COVID-19 “vaccines.”
The proper conduct of these approval procedures requires full transparency and that the precautionary principle be applied. Absolute transparency is in everyone’s best interest, and in an open, democratic society should be by both the authorities and the people. However, it has been established that the well-defined procedures for the approval of new medicines, and the standards of transparency and of due diligence which are necessary to safeguard them, have been violated in connection with the authorizations of the COVID-19 “vaccines.” These violations need to be mended with urgency.
The lack of transparency, on the part of the national and EU authorities in their authorizations of the mRNA products, is putting the entire population, now also including the children, at serious risk. In order to restore the missing transparency, CHD Europe is submitting a comprehensive FOIA request.
Dr. Renate Holzeisen, Children’s Health Defense Europe has filed this FOIA request on 22nd July 2022 to the EU, EMA and European Commission, as well the the two Italian authorities responsible for fundamental public health (the national Ministry of Health, Istituto Superiore della Sanità and Aifa). These authorities are requested, with urgency, to disclose information on the so-called mRNA “vaccines” against COVID-19, namely, Comirnaty from Pfizer-BioNTech and Spikevax from Moderna.
There is plausible and experimental evidence that the mRNA contained in Pfizer/BioNTech’s Comirnaty and Moderna’s Spikevax “vaccines” can be back-transcribed into DNA and then be inserted into the human genome. Such insertion events will cause gene mutations, which may lead to cancer and leukemia. The scientific opinion attached to our F.O.I.A. shows that reverse transcription from RNA into DNA, followed by insertion into the cells’ chromosomes, is a mechanism that has been known for many decades. It must also be assumed that the risk of reverse transcription, insertion, and mutagenesis increases with each further inoculation. Please read the scientific report of evidence here.
Furthermore, since it has been proven experimentally that the actual nature and function of the two substances Comirnaty and Spikevax can lead to an alteration of the human genome, it is clear that the “labelling” of the substances has been erroneous.
The two mRNA substances have been formally categorized as “vaccines”, even though overwhelming data and facts show that they do not fulfil the function of a vaccine. The mislabeling of these two substances as “vaccines against infectious diseases” excluded them from the regulators’ formal definition of gene therapy, which was then used to justify the omission of testing for genotoxicity, carcinogenicity and mutagenicity.
It is clear that these mRNA COVID-19 “vaccines” have exactly the mechanism of a gene therapy drug, since the inoculated mRNA is intended to change the protein expression of the human body cells so as to produce the spike protein. Moreover, since they do not actually have the function of traditional vaccines for the prevention of infectious diseases, the safety studies to be carried out by the manufacturers should have been subject in their entirety to the more restrictive provisions for advanced therapy products (as provided for in recital 10 of Reg. EC No. 1394/2007). Finally, this more extensive documentation should have been submitted for evaluation to the EMA’s Committee for Advanced Therapies, since only that Committee guarantees, or at least should guarantee, the specific expertise that is necessary to evaluate substances that affect cell physiology through a genetic mode of action.
By permitting and encouraging or even mandating the repeated inoculation of these experimental substances, which have the potential to mutate the human genome, the national and EU authorities are placing the entire population, including children, at serious risk. To remedy this situation, there is an urgent need for absolute transparency.
To that end, CHD has requested the urgent release of the following:
1. The documentation proving the involvement of the Committee for Advanced Therapies in the respective procedure of the conditional marketing authorization of the two mRNA substances, Pfizer/BioNTech’s Comirnaty and Moderna’s Spikevax, as well as the opinion issued by the Committee for Advanced Therapies on the aspect of genotoxicity and/or related carcinogenicity risks, as well as on the mutagenicity of these two substances.
2. The documentation proving the evaluation (including the respective outcome) of the genotoxicity, carcinogenicity and mutagenicity of the two substances Comirnaty by Pfizer/BioNTech and Spikevax by Moderna.
3. To the addressees of the Italian institutions Ministry of Health, Istituto Superiore della Sanità and AIFA, in addition to the above, we also requeste: the opinion of the Government’s Technical Scientific Commission on the genotoxicity, carcinogenicity and mutagenicity of the two mRNA substances, Pfizer/BioNTech’s Comirnaty and Moderna’s Spikevax.
For information, please contact:
press@chdeurope.org
Documentation in English, click here.
Documentation in Italiano, click here.
Dr. Holzeisen, human rights lawyer, is based in Italy. She is a member of the board of Children’s Health Defense Europe and is also President of the Italian Legal Confederation for Human Rights (Confederazione legale per i Diritti dell’Uomo).
Executive Summary of the Submitted F.O.I.A. Request
Children’s Health Defense Europe have submitted an urgent F.O.I.A. request by our board member, Dr. Renate Holzeisen, to the EU (EMA and European Commission) and national (Italian Ministry of Health and Istituto Superiore della Sanità and Aifa) authorities responsible for public health to obtain fundamental information on the so-called Covid-19 mRNA “vaccines” (Comirnaty from Pfizer-BioNTech and Spikevax from Moderna).
Since the injection of these two substances into the body causes the nucleic acid contained in the two substances to cause the production of a specific spike protein (that of the SARS-CoV-2 virus) within the framework of so-called cellular protein expression, and this mechanism corresponds exactly to what EU regulations require for so-called gene therapy medicinal products.
There is plausible and experimental evidence that the mRNA contained in Pfizer/BioNTech’s substance Comirnaty can be retro-transcribed into DNA and can insert itself into the human genome. We have attached to our request a scientific report setting out this evidence, recalling the decisive facts in this regard established in science some time ago.
Contrary to what was officially declared to the population by the institutions responsible for the “vaccination” campaign, this synthetic mRNA does not remain in the muscle of the arm where inoculation takes place...
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The mission of Children’s Health Defense Europe is to restore and protect the health of children and adults by eliminating exposures to environmental toxins, holding responsible parties accountable, and establishing safeguards to prevent future harm to health. The association also wishes to defend the respect of human rights, fundamental freedoms and democratic principles in health practices and policies, in particular by promoting the principles of free informed consent and freedom of care, the respect of privacy, freedom of science and transparency.
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