Antionette Johnson is a Consumer Safety Officer in the Office of Compliance, Division of Bioresearch Monitoring (BIMO), at FDA’s Center for Devices and Radiological Health (CDRH). She has been managing the Good Laboratory Practice (GLP) compliance program for nonclinical studies since March 2017. Prior to joining CDRH, she was a Consumer Safety Officer in the Office of Compliance and Enforcement at the Center for Tobacco Products and she worked in quality assurance at a pharmaceutical company.