The political firestorm engulfing the US Food and Drug Administration continues, with its chief spokesperson, Emily Miller, being sidelined following fierce criticism of the way the agency handled an emergency use authorization for COVID-19 convalescent plasma. The situation shows the consequences of FDA straying from its strictly science-based approach and the turmoil going on within the agency as it deals with pressures inside and outside the Trump Administration.
The sidelining of Miller, first reported by the New York Times, suggests she was being held accountable, at least in part, for the agency’s rollout of the emergency use authorization. FDA issued a terse one-sentence statement on 28 August: “Ms