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What is Phases of Pharmacovigilance Explained about?

The document provides an overview of pharmacovigilance. It defines key terms like adverse drug reactions and outlines the drug development process from preclinical testing through post-marketing surveillance. Clinical trials have limitations in detecting adverse events, so pharmacovigilance is needed both during trials and after approval to monitor drug safety based on larger, real-world use. Reporting of adverse events by healthcare professionals, consumers and manufacturers helps identify new safety issue

Author

abdullah2020

Language

EN