Pharmaceutical Legislation
/ˌfɑːrməˈsuːtɪkəl ˌlɛdʒɪsˈleɪʃən/
Definitions
- (n.) The body of laws and regulations governing the development, approval, manufacturing, marketing, and distribution of pharmaceutical drugs.
Pharmaceutical legislation ensures drug safety and efficacy before products reach consumers.
Forms
- pharmaceutical legislation
Related terms
See also
Commentary
Typically encompasses regulatory frameworks such as FDA rules in the US or EMA regulations in the EU; drafters should specify jurisdiction due to variation in legal regimes.
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.