Pharmacovigilance is required through the entire life cycle of a drug – starting from preclinical development stage, going through continues monitoring till regulatory approval as well as spanning post-market stidues. Discover with Meditrial all aspects of European Pharmacovigilance and Drug Safety that include collecting, analyzing, monitoring, and preventing adverse effects in new drugs and therapies. Upon completing a course, you will take a final test to receive a digital certificate that can be printed.

In this course you will get an overview of worldwide pharmacovigilance standards. Here we also talk about the main goals of pharmacovigilance in clinical research. In addition, we will shed the light on various ways how one can ensure the safest use of a drug and its compliance with the legal requirements on pharmacovigilance. Upon completing a course, you will take a final test to receive a digital certificate that can be printed.