COVID-19 Injection Campaign Violates Bioethics Laws || An Interview With Dr. Robert Malone !!

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CREDIT:

Host: Dr. Joseph Mercola
Guest: Dr. Robert Malone
Topic: COVID-19 Injection Campaign Violates Bioethics Laws
Show: Mercola - "Take Control Of Your Health"
Date: Sunday, August 1st, 2021
Transcript: https://bit.ly/3yDU5pB
Website: https://bit.ly/3xBhbvF
Bitchute Video: https://bit.ly/3jKqa8O

DESCRIPTION:

Dr. Robert Malone, who is, truly, one of the most respected experts in this and that he is really the inventor of the messenger RNA vaccine. He is really a true insider. We have somewhat differing views with respect to vaccines. He is a pro-vaccine person and actually has received the COVID vaccine himself. But he actually developed the platform, the technology that allows the mRNA vaccine to exist.

CONCERNS:

• Safety data analysis and reporting in clinical trials of the COVID jabs appear to have been manipulated in at least some cases. One method for manipulating randomized clinical trial safety data is to only analyze the “per protocol” treatment group (those who completed all doses and were fully compliant with the study design) as opposed to “intent to treat” which would include all patients that have signed informed consent.

• For example, if a participant only accepted one dose and trial protocol called for two, under a “per protocol” analysis, adverse events they experienced would be dismissed and not included in the safety analysis. This is a classic way to manipulate safety data in clinical research, and it's usually forbidden.

• Since the COVID shots only have emergency use authorization, they are experimental products and, as such, they are not authorized for marketing.

• Bioethics are written into federal law. As an experimental trial participant, you have the right to receive full disclosure of any adverse event risks. Full disclosure of risks is not being done, and in fact is being suppressed.

• Adverse event risks must also be communicated in a way that you can comprehend what the risks are, and the acceptance of an experimental product must be fully voluntary and un-coerced. Enticement is strictly forbidden.

QUOTE:

"There's the appearance that there was manipulation of safety data analysis and reporting in the Phase 1, 2, 3 clinical trials … by focusing on patients who had completed the study per protocol, as opposed to those that entered the study as intended to treat. [ If ] you've only accepted one dose of vaccine under those clinical trial protocols and you have an adverse event … that information about the adverse event … is lost. It's not included in the safety analysis. This is a classic way to manipulate safety data in clinical research, and it's strictly forbidden."