Vaccine Experiment Atrocity: Human Infection Model

Home / Vaccines / Vaccine Experiment Atrocity: Human Infection Model

Vaccine Experiment Atrocity: Human Infection Model

by Vera Sharav
October 16, 2019


It appears that vaccine manufacturers are ever more impatient to reap high profits from new vaccines — especially since they have entered into “public-private” partnerships with governments. Increasingly, government officials oblige this greed-infected industry with laws mandating new vaccines. And public health authorities around the globe have become marketing auxiliaries for vaccine manufacturers.

A report in the Economic Times of India, confirms that the Indian health ministry is working with the Indian Council of Medical Research (ICMR), the Department of Biotechnology, and the Drug Controller General of India (DCGI) as they embark on a medical atrocity – that is, to conduct clinical trials in which human beings are deliberately infected with deadly diseases in order to test the efficacy of experimental vaccines. The India Infection Research Consortium has named these experiments: “controlled human infection model (CHIM)”

This “controlled human infection model” is no different than the medical atrocities committed by the medical establishment under the Nazi regime.

India’s public health officials declare that the CHIM atrocity will abide by “high standards of medical ethics.”

Which standards of medical ethics?

The Nuremberg Code is the most important document in the history of the ethics of medical research.

3. “The experiment should be so designed and based on the results of animal experimentation and a knowledge of the natural history of the disease or other problem under study, that the anticipated results will justify the performance of the experiment.”

ndia will be hosting a gathering  in November to work on broad guidelines for “controlled human infection model” (CHIM) experiments.

The conference will include an international roster of researchers and regulators. The invited regulators include representatives of the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA), the U.K. Medicines and Healthcare products Regulatory Agency (MHRA),  and experts from the World Health Organization (WHO). They will be collaborating and lending the veneer of legitimacy to a medical atrocity.