C19 VACCINES CONFIRMED AS GMO & ILLEGAL PRODUCTS - BOMBSHELL!!!!
Report 98: FDA Selected Its Committee' - Not Its Gene Therapy Advisory Committee - to Recommend the COVID Injections for Emergency Use and Hid the Nature of Products.
THIS LATEST NEWS will come as a bombshell to the millions of people who trusted the authorities in taking what has been determined by lawyers to have been a GMO - a gene-altering drug which changes DNA.
Dr John Campbell Investigates:
Thanks to the dogged and conscientious research of lawyers and barristers like Julian Gillespie, it has been determined that during the COVID-19 debacle, both government and pharmaceutical companies hid the facts from the public that now state that the vaccines were GMO products which are not only gene-altering but DNA changing products.
This means that those involved with coercing the public into taking the products through the staged Western governments fear campaigns have literally destroyed the lives of thousands if not millions of people and, says Mr Gillespie, they should now be held accountable and personally liable for their decisions.
Barrister Julian Gillespie, LLB from Australia, says the GMO laws throughout the Western world are virtually ‘word for word’ the same.
He has just finished global legal research into GMO laws and says that the UK, South Africa, and the EU have similar GMO legislation to Australia. Those jurisdictions variously flouted their GMO laws (the UK and SA) or illegally ignored them (Australia and the EU).
For the UK situation, Mr Gillespie has documented everything in a legal opinion for Andrew Bridgen MP, and his findings on what occurred in the EU are set out in his peer-reviewed paper. Here is an abridged version
Go to Julian Gillespie’s Substack here:
The Canaries in the Human DNA Mine.
Legal action against Pfizer and Moderna
Mr Gillespie has also been spearheading with Katie Ashby-Koppens and Dr Julian Fidge the now extraordinary legal action against Pfizer and Moderna here in Australia for their Covid drugs fulfilling Australian legal definitions for being deemed GMOs, requiring GMO licenses (which they did not seek nor were granted), all of which the Australian government knew prior to provisionally approving them.
“The Australian government did not inform Australians of these facts”.
Mr Gillespie states that the COVID-19 'vaccine' drugs are modified mRNA gene therapy products. So, why did the FDA assign the review and recommendation responsibilities to the Vaccines and Related Biological Products Committee (VRBPAC) instead of the Cellular Tissue and Gene Therapy Advisory Committee (CTGTAC)? CTGTAC was the logical FDA advisory committee for such a product. Yet the FDA insisted on calling the COVID-19 gene therapy injections 'vaccines' and assigned them to VRBPAC.
Report 98: FDA Selected Its 'Vaccines Advisory Committee' - Not Its Gene Therapy Advisory Committee - to Recommend the COVID Injections for Emergency Use, Hid Nature of ProductsCOVID-19 'vaccine' drugs are modified mRNA gene therapy products.
In September 2021, the Centers for Disease Control and Prevention (CDC) in the United States changed the definitions of ‘vaccine’ and ‘vaccination’ to match the output measurement (i.e., antibody titers) of the mRNA products. To date, the CDC has not logically justified its changes to those definitions, and the FDA has not explained why it selected a vaccine advisory committee to review and approve gene therapy products.
The question on people's lips should surely be, ‘What are the roles and purposes of the various FDA committees? Are they in place to support Big Pharma or to protect the American people?’
Graham Bridger
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