QPPV Services
Qualified Person for Pharmacovigilance (QPPV) The Qualified Person for Pharmacovigilance (QPPV) plays a critical role in ensuring the safety of pharmaceutical products. As the designated expert responsible for pharmacovigilance activities within a company, the QPPV oversees the collection, evaluation, and reporting of adverse drug reactions and other safety-related information.
Their expertise and thorough understanding of regulatory requirements enable them to establish robust pharmacovigilance systems, ensuring compliance with applicable laws and guidelines. By serving as the primary point of contact for regulatory authorities and coordinating risk management activities, the QPPV safeguards public health and contributes to the continuous monitoring and assessment of the benefit-risk profile of medicinal products.
Responsibilities of a Qualified Person for Pharmacovigilance (QPPV) are:
Keep track of regulatory legislation and ensure pharmacovigilance compliance guidelines
Facilitate communication with healthcare professionals, patients, and regulatory agencies regarding drug safety issues.
Assess and manage risks associated with medicinal products throughout their lifecycle and implement risk minimization measures and develop risk management plans.
