pharmacovigilance translation

Pharmacovigilance and Postmarketing Sureveillance Translation Use Case

Accurate translation of pharmacovigilance and postmarketing surveillance documents—such as adverse event reports, periodic safety update reports (PSURs), and risk management plans—is essential to monitor drug safety, maintain regulatory compliance, and protect patients worldwide after product approval.

pharmacovigilance translation

Case Study

Getting Ahead of the IVDR Tsunami

Download our white paper on protective strategies for navigating regulatory upheaval, translation demands and the evolving landscape of EU in vitro diagnostic compliance.