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Sonja Brajovic

Medical Officer, Office of Surveillance and Epidemiology, CDER
Sonja Brajovic is a Medical officer in the Office of Surveillance and Epidemiology (OSE), Center for Drug Evaluation and Research (CDER), U.S. Food and Drug Administration (FDA). She is responsible for coordination of projects related to the Medical Dictionary for Regulatory Activities (MedDRA), including monitoring MedDRA coding quality of reports in the FDA Adverse Event Reporting System (FAERS). Sonja represents FDA on the International Conference on Harmonisation (ICH) MedDRA Points to Consider workgroup and the Council for International Organizations for Medical Sciences (CIOMS) Implementation workgroup on Standardised MedDRA Queries (SMQs). Sonja obtained her medical degree in the former Yugoslavia.