This course delves deeper into the regulatory landscape of Good Pharmacovigilance Practices (GVP), focusing on the guidelines that safeguard the safety and effectiveness of medicinal products throughout their entire lifecycle. Participants will explore core concepts, regulatory obligations, and best practices in pharmacovigilance, gaining valuable insights into the processes that ensure patient safety through the effective monitoring and management of drug-related risks. Upon completion, learners will have a comprehensive understanding of GVP principles and their crucial role in the pharmaceutical sector.