This course provides a comprehensive
foundation in science and activities relating to the detection, assessment,
understanding, and prevention of adverse effects or any other drug-related
problems, forming a critical component of patient safety and public health.
Participants will learn the global regulatory framework governing
pharmacovigilance, master the processes for adverse event reporting and
management, and develop skills in risk assessment, signal detection, and the
development of risk minimization strategies. By understanding the entire
pharmacovigilance lifecycle, from clinical trials to post-marketing
surveillance, you will be equipped to ensure the ongoing safety of
pharmaceutical products and contribute to the safe and effective use of medicines
for patients worldwide.