House hearing exposes Biden FDA 'politicization,' fallout of rushed COVID vaccine approval for kids, military

A House Judiciary subcommittee hearing Wednesday addressing the "politicization" of the U.S. Food and Drug Administration (FDA) during the pandemic exposed how the Biden administration allegedly pressured medical professionals to expedite the COVID-19 vaccine for children before enough testing was completed to confirm or deny its safety.

At the onset of the subcommittee hearing, "Follow the Science?: Oversight of the Biden COVID-19 Administrative State Response," Chairman Thomas Massie, R-Ky., read from past testimony of Dr. Marion Gruber, the former director of the FDA’s vaccine office, regarding conversations she had with Dr. Peter Marks, the agency’s top vaccine regulator, about the efficacy of the COVID vaccine in children. Massie said Gruber expressed a need for more trial testing in the pediatric population, specifically among males ages 12 to 17, but Marks allegedly pushed to further compress the schedule to license the vaccines so they could be mandated.

"Right when they were getting the warnings that myocarditis and pericarditis are real and serious side effects to the vaccine, the top scientists at FDA had already agreed to compress the schedule as much as possible, right when they got the message that there were serious side effects," Massie said. "And Peter Marks, instead of telling them, 'We’re going to give you more time to study this,' he told them to compress the schedule even more.

"And when they said that compressing the schedule was not possible, he fired them. He took them off the job, he assigned them to other duties. The top vaccine officials who had been there for 30 years, taken off the job because they wanted more time to study the effects of the vaccines. And they were told they needed to do this