Supporting Your Regional Pharmacovigilance Needs with Our QPPVs & LPPVs

A Qualified Person Responsible for Pharmacovigilance (QPPV) is an individual who is appointed by a pharmaceutical company to ensure the compliance of its pharmacovigilance system with regulatory requirements. The QPPV is responsible for overseeing the safety of the company’s medicinal products and ensuring that any adverse events related to the use of these products are reported and handled in accordance with applicable regulations.

LPPVs are responsible for the local implementation of pharmacovigilance activities in individual countries, including the collection and reporting of adverse event data. They work closely with QPPVs to ensure that safety information is communicated effectively across borders.

We deliver QPPV & LPPV services leveraging our TOTALVigilance framework and our affiliates, staretgic partners across the globe a cost-effective, flexible, and scalable solution designed to enhance your regulatory complaince and real-time oversight. It combines qualified resources,  knowledge, lean processes, and modern technology to deliver high-quality, compliant services. With adaptable service models and seamless integration into your existing systems and workflows, TOTALVigilance enhances operational efficiency, enables proactive oversight, and maximizes return on investment.