Drug safety training is essential for professionals involved in pharmacovigilance, clinical research, and regulatory affairs. It equips individuals with the knowledge and skills to monitor, assess, and report adverse drug reactions (ADRs) and ensure the safety of pharmaceutical products throughout their lifecycle.

The training typically covers topics such as pharmacovigilance principles, risk management, adverse event reporting, regulatory guidelines, and global safety standards. It also emphasizes the importance of compliance with international regulations, such as those set by the FDA, EMA, and WHO.

Drug safety training programs are valuable for healthcare professionals, researchers, and pharmaceutical industry employees seeking to contribute to patient safety and enhance public health.