Definition: the pharmacological science relating to the detection, assessment, understanding, and prevention of adverse effects, particularly long-term and short-term side effects of medicine.

Our total medical affairs solution is built on a strong foundation of providing pharmacovigilance support. We offer a complete MedWatch reporting solution, with signature- and FDA-ready MedWatch documents and quarterly summaries. We have a staff skilled at managing compliance reporting requirements and time frames, and we follow up all reports with the goal of complete information capture.

Our Adverse Event Management software provides a validated full data management environment, including auto-reminders to staff regarding reporting requirements. The pharmacovigilance program is seamlessly integrated with our Corporate Contact Center operation.