| The Introduction to Drug Safety module provides the basics of pharmacovigilance, its regulation throughout all stages of the drug life cycle, and the foundation knowledge required to work day-to-day in clinical safety and the pharmacovigilance industry.
The module includes the historical overview of drug safety legislation, from the beginning to the current international standards; basic definitions and tools of adverse events and adverse drug reactions recording, assessment and reporting, as well as pharmacological mechanics of drug safety. The second part of the module provides the basic skills of pharmacovigilance documentation management, including safety reports, reference safety information, and post-marketing labeling preparation and handling. | 
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