USA: +1 617 939 9497 | EU: +34 607 939 266 info@sofpromed.com

Pharmacovigilance Services for Clinical Trials 

Sofpromed provides pharmacovigilance services for pharmaceutical and biotechnology companies dedicated to the development of new drugs. We manage adverse events (monitoring, listings, and reporting) through a fully E2B (R3) compliant safety database.

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Drug Safety Services

Adverse event (AE), serious adverse event (SAE), and serious unexpected suspected adverse reaction (SUSAR) monitoring, SAE management and reconciliation, SUSAR reporting, EudraVigilance reporting, safety database management, and writing of annual safety reports (DSURs).