How Validcare Kept Safety Reporting on Track with PiVOT’s Support
Learn how PiVOT partnered with Validcare to maintain uninterrupted pharmacovigilance operations during an active clinical study. By rapidly integrating into the client’s workflows, PiVOT processed more than 1,000 adverse events while consistently meeting 48-hour coding timelines and supporting evolving regulatory requirements.
PiVOT’s Role In A Multi-Country Phase III GI Trial
Executive Summary A European pharmaceutical sponsor initiated a multi-country phase 3 confirmatory trial to evaluate the efficacy and safety of a once-daily gastrointestinal drug. Its primary contract research organization (CRO) for Southeast Asia and Eastern Europe selected PiVOT to manage operations in the Philippines because of its regulatory expertise, strong site relationships, and a record […]