Our pharmacovigilance audit service offers a comprehensive analysis of the processes and systems related to drug safety management. We specialize in assessing compliance with regulatory standards and good pharmacovigilance practices (GVP), identifying areas for improvement and potential risks in the management of adverse events (AE) and public health risks. Our highly trained auditors perform both internal and external audits, tailoring the approach to the specific needs of each client and providing practical recommendations and effective solutions to strengthen pharmacovigilance processes.

Furthermore, our expertise extends to auditing external suppliers and business partners in relation to their pharmacovigilance activities, ensuring they meet regulatory requirements and quality standards. We are committed to ensuring the integrity and reliability of the data collected, managed, and reported in the context of pharmacovigilance, thus contributing to the protection of public health and compliance with regulatory obligations. Our audits provide a comprehensive view of the effectiveness and robustness of pharmacovigilance systems, allowing our clients to continuously improve their practices and processes to ensure the safety and quality of their pharmaceutical products.