FDA’s Peter Marks appeared before a House panel on Thursday to field questions on how to improve the nation’s vaccine safety systems in the event of another public health emergency. He didn’t make it out without getting caught in the political crossfire over vaccine misinformation.
Marks, who leads the agency’s Center for Biologics Evaluation and Research, testified before the House Oversight Committee’s coronavirus select subcommittee. During his testimony, he highlighted challenges that the FDA faced in getting real-time vaccine safety data throughout the pandemic.
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