Pharmacovigilance
Build your pharmacovigilance knowledge from the ground up with our comprehensive three-day course and prepare yourself to contribute in a field where the demand for expertise is growing.
Our recurring Nordic-Baltic conferences help you stay up to date with the latest developments in a field that is rapidly evolving, where the role of AI may become even more central.
Pharmacovigilance - Basic course
The course gives a broad and basic knowledge and understanding of the drug safety area and its current legislation. Suitable for those new to their role and those already active in the field, whishing to update their knowledge and discuss the application of current regulations.
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Are you interested in Regulatory Affairs too?
We offer a wide range of courses for both newcomers and experienced professionals in the field of regulatory affairs.
What is pharmacovigilance?
Pharmacovigilance is the science of collecting, detecting, assessing, monitoring, and preventing side effects of drugs. Before a medicine is approved, it is tested in clinical trials under controlled conditions in order to be able to measure the effects accurately. When the drug is finally approved, many more factors play a role in the drug’s intended and unintended effects and in interactions with other drugs. That is why it is of utter importance that a medicine is continously monitored even after approval for use.
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