Organised Crime via Vaccines: Professor Masayasu Inoue of Osaka University Medical School

8 months ago
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Prof. Masayasu Inoue (WCH Japan) warns of official plans to shorten the time period for the development of new vaccines (especially those using an mRNA platform) from 5-10 years to 100 days. Prof. Inoue (professor em. of the Osaka University Medical School, specialty: molecular pathology and medicine) says that during COVID "under the pretext of saving time, an extremely dangerous [medical] method was selected. That is the intra-muscular injection of viral genes that produce toxic spike proteins directly in human tissues to stimulate the immune system. Because this is a completely new method and a misguided concept that has never been applied in human history before, it is impossible for most of the doctors to ensure proper informed consent."

Prof. Inoue continues: "However, due to irresponsible government and media campaigns to promote vaccination, 80% of the Japanese have been vaccinated, unfortunately ... The result was the induction of terrible drug-induced injuries ... I believe that the fraudulent use of experimental gene therapy in healthy people, especially healthy children, is an extreme violation of human rights."

World-renowned physicians and scientists are calling for the mRNA COVID products to be pulled due to safety concerns and lack of efficacy. At the same time, vested interests regard these products as a business model for the future.

Prof. Inoue warns of official plans to generally shorten the time period for the development of new vaccines (especially those using an mRNA platform) from 5-10 years to 100 days. He says that his country Japan, for example, is building factories for rapid mass vaccine production in preparation for a Disease X scenario and that he personally visited those factories. He believes that Japan is implementing policies originating from the Coalition for Epidemic Preparedness Innovations (CEPI).

CEPI, led by Richard Hatchett who once worked under Anthony Fauci, was founded in 2017 by the private, unaccountable World Economic Forum (WEF), the Bill & Melinda Gates Foundation and others to shorten the vaccine development process to a mere 100 days. In comparison, regular vaccine development takes 5 to 10 years in which safety and efficacy are assessed in clinical trials, regulatory approval processes are passed and widespread manufacturing requiring certain standards to avoid contamination is initiated.

While certain therapeutics should be made available in an accelerated manner to those that want to try them in life-threatening or life-altering situations (Right to Try), the lessons of COVID show that reducing regulatory standards for the population-wide approval of novel products that are in an experimental phase carries considerable and even fatal safety risks. This applies all the more when the potential of severe side effects and contamination is being censored by governments and private stakeholders financially invested in said products. An added concern relates to the fact that governments – invested in little understood, fast-tracked experimental mRNA products approved for emergency use – sought to mandate their uptake and override the informed consent process, utilizing systematic coercion and propaganda.

VIDEO AND TEXT SOURCE: https://twitter.com/lawrie_dr/status/1774467798485410133

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