"Great learning experience with a strong focus on pharmacovigilance practices."

I really appreciated the way the sessions connected theory with real-world applications. The case studies on post-marketing surveillance and regulatory compliance helped me link my academic background in drug development and clinical trials with practical challenges faced in industry. The speakers made complex concepts related to safety monitoring, adverse event reporting, and compliance frameworks very clear, which was particularly useful for someone like me preparing for a career in pharmaceutical quality and safety.