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Summary:
Dr. med. Wolfgang Wodarg is a lecturer at the University of Flensburg and has acted within the Parliamentary Assembly of the Council of Europe Health Committee where he co-signed a proposed resolution titled ‘Faked Pandemics - a threat for health’ on 18 December 2009, which was briefly discussed in January 2010 in an emergency debate. Wodard has called for an inquiry into alleged undue influence exerted by pharmaceutical companies on the World Health Organization’s global H1N1 flu campaign
Dr. Michael Yeadon is a highly experienced, innovative drug discoverer with 25y+ in the pharmaceutical industry. He was “Chief Scientific Officer” and the head of “Allergy & Respiratory Research” for Pfizer.
Both men are extremely experienced in their respective field and both petitioned the European Medicines Agency in December 2020 to ask for a ‘Stay of Action’ with regard to licensing a COVID-19 vaccine.
They cited the use of PCR as a diagnostic tool for determining COVID-19 infection in the placebo group. They claimed that the ‘false-positive’ rate of the PCR would “artificially raise the efficacy of the vaccine, unless the RTqPCR test results are verified by nucleotide sequencing to eliminate all false-positive test results.”
In order to leave “no excuse for the Sponsor to refuse using the gold-standard Sanger sequencing technology for endpoint validation” they offered “to re-test them immediately with ‘Sanger sequencing’ and submit the laboratory data to support FDA’s evaluation.”
They clarified their concerns by adding that “based on the scientific data available in the public domain and the FDA guidance, all RT-qPCR test results for detection of SARS-CoV-2 gene sequence must be considered presumptive. The Cepheid test kits for SARS-CoV-2 are known to generate more false-positive test results than other EUA assay kits.”
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