Overview
![DIA Learning](/en/-/media/diaglobal/images/tiles/323x240/courses/learning-lms-face-to-face-default-323x240.jpg?sc_lang=en)
This course is designed to provide a firm grounding in key aspects of European Clinical Pre- and Post-Marketing Safety regulatory requirements. This five-day training course also includes highlights and updates on the pharmacovigilance legislation and the latest news on the international harmonisation and standardisation activities in pharmacovigilance.
"The course was well organized, with active sessions leading to open discussions. The teachers were creating an environment that was facilitating the open confrontation and providing examples in order to facilitate the comprehension."
Ilaria Giunzioni, Drug Safety Manager, Grunenthal
"I think with this course you learn a lot and is very useful for a person who is working in pharmacovigilance."
Itziar López-Oleaga, Pharmacovigilance Technician, PHARMAMAR
Program Committee
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Gaby L. Danan, MD, PhD Pharmacovigilance Expert
GLD, France -
Phil Tregunno Deputy Director - Patient Safety Monitoring
Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
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