The petition, which had garnered 326 comments as of press time, cites evidence that the Pfizer and Moderna COVID-19 vaccines are unapproved gene therapies and are contaminated with DNA plasmids.
Scientists and legal experts have petitioned the U.S. Food and Drug Administration (FDA) to suspend or withdraw the Pfizer and Moderna mRNA COVID-19 vaccines, arguing they are unapproved gene therapies and citing their contamination with DNA plasmids.
According to a press release by Australian law firm PJ O’Brien & Associates, the petition “exposes alarming evidence of synthetic DNA contamination and regulatory failures that could affect millions worldwide,” shedding light on “a public health crisis.”
The Citizen Petition stated that Pfizer and Moderna misclassified their mRNA products as vaccines instead of gene therapy products, enabling the companies to avoid legally required FDA environmental assessments.
“This misclassification denied Americans transparency and informed consent, violating federal law and rendering approvals void from the start,” the press release stated.
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