Pharmacovigilance
/ˌfɑːrməkoʊˌvɪdʒɪˈlæns/
Definitions
- (n.) The legal and regulatory monitoring of adverse effects and safety of pharmaceutical products post-marketing to ensure public health.
Pharmacovigilance protocols require companies to report serious drug side effects to regulatory authorities promptly.
Forms
- pharmacovigilance
Related terms
See also
Commentary
Pharmacovigilance is critical in legal frameworks governing pharmaceuticals to balance patient safety and market access; clear legal definitions help ensure compliance with regulatory obligations.
This glossary is for general informational and educational purposes only. Definitions are jurisdiction-agnostic but reflect terminology and concepts primarily drawn from English and American legal traditions. Nothing herein constitutes legal advice or creates a lawyer-client relationship. Users should consult qualified counsel for advice on specific matters or jurisdictions.