Medicinal Product Regulation
/ˌmɛdɪsɪnəl ˈprɒdʌkt ˌrɛɡjʊˈleɪʃən/
Definitions
- (n.) The body of laws and regulations governing the approval, manufacture, distribution, and marketing of pharmaceutical products to ensure their safety, efficacy, and quality.
Pharmaceutical companies must comply with medicinal product regulation before launching a new drug in the market.
Forms
- medicinal product regulation
Related terms
See also
Commentary
Medicinal product regulation typically encompasses statutory and administrative frameworks designed to protect public health by controlling medicinal substances; drafters should be precise about jurisdictional scope and procedural requirements.
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.