June 2025

As someone who has spent many years working across different regions and regulatory environments, I can say that the pharmacovigilance (PV) landscape in the Rest of the World (RoW) is quite complex and diverse. Unlike the US or Europe, where regulations are well-established and enforcement is consistent, many countries in the RoW are still developing…

In the rapidly evolving field of pharmacovigilance, maintaining a robust Quality Management System (QMS) is critical, not only for ensuring regulatory compliance and safeguarding patient safety, but also for driving continuous improvement. With over two decades of experience in drug safety and clinical research, I’ve learned that the success of a QMS is not solely…