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for Pharmaceutical and Medical Devices Professionals
Pharmacovigilance courses deal with the latest news on the evaluation and prevention of adverse events or other medical related events, to ensure a good benefit/risk profile for patients: regulations in place, strategy, methodology and even the use of artificial intelligence in the field of pharmacovigilance. These trainings are designed for clinical research professionals who wish to know more about Pharmacovigilance or for those already in the field who need a high-level training. Courses on Pharmacovigilance are held as interactive workshops, with lectures, discussions and exercises.
ONLINE TRAINING: Pharmacovigilance Documents in the Life Cycle of a Medicinal Product: From Patients to Health Authorities
Development Safety Update Report (DSUR), Risk Management Plan (RMP), Periodic Safety Update Report (PSUR) / Periodic Benefit-Risk Evaluation Report (PBRER), and Addendum to the Clinical Overview