adverse event

Adverse Event Translation Use Case

Pharmaceutical and medical device companies rely on accurate translations of adverse event (AE) source documents to meet regulatory requirements, ensure patient safety, and facilitate global reporting. Fast, precise, and compliant translations help streamline pharmacovigilance processes and prevent delays in drug and device approvals.

adverse event

Case Study

Precision Patient Communication

See how Puma Biotechnology improved compliance, engagement, and clarity using validated Spanish medical translations.