GoBroad Clinical Research Center's Pharmacovigilance team consists of professionals with medical and pharmaceutical backgrounds, with solid experience in the industry. Our team provides end-to-end pharmacovigilance services covering the whole drug lifecycle from clinical development to post-marketing, including establishing pharmacovigilance systems, handling individual case safety reports (SUSAR, ADR, etc.), writing and submitting aggregate safety reports (DSUR, PSUR, PBRER, etc.), safety signal detection and risk management, and pharmacovigilance audits. Our team is committed to providing expertise and customer-oriented services, ensuring fully compliant submissions.