Medicinal Regulation
/ˌmɛdɪˈsɪnəl ˌrɛɡjʊˈleɪʃən/
Definitions
- (n.) The body of laws and regulatory frameworks governing the production, distribution, and use of medicinal substances.
The medicinal regulation ensures that all drugs meet safety standards before reaching consumers.
- (n.) Legal oversight and control measures imposed to ensure the efficacy, safety, and ethical marketing of medicines.
Medicinal regulation protects public health by mandating rigorous testing of pharmaceuticals.
Forms
- medicinal regulation
Related terms
See also
Commentary
This term typically appears in regulatory and health law contexts and often involves multiple governmental agencies responsible for enforcement.
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.