Pharmacovigilance

Safety is our first priority in every clinical trial we conduct. Our pharmacovigilance group, run by physicians, provides around-the-clock coverage and medical oversight. We employ the latest technologies and safety databases for tracking adverse events and serious adverse events, including Clintrace®, Oracle® AERS, and the EVWEB reporting tool. We comply with ICH guidelines by using MedDRA, the industry standard in medical terminology and medical coding.

We also provide pharmacovigilance support as a stand-alone service at the request of our clients.