'The FDA’s abject failure to address these risks in a serious manner... have once again damaged the credibility of the US HHS in the eyes of both the US public and the world,' Malone stated.
The FDA did not seek approval from its Vaccines and Related Biological Products Advisory board before granting emergency use authorization for booster shots in 5-year-olds, arguing that its research 'did not raise questions that would benefit from additional discussion by committee members.'
Can a COVID-19 vaccine approval process marked by such egregious and numerous conflicts of interest refrain from compromising public health and safety?