Medicinal Products Regulation
/ˌmɛdɪˈsɪnəl ˈprɒdʌkts ˌrɛɡjʊˈleɪʃən/
Definitions
- (n.) A body of law and regulations governing the authorization, production, distribution, and supervision of medicines to ensure safety, efficacy, and quality within a jurisdiction.
The Medicinal Products Regulation sets strict standards for pharmaceutical companies seeking market approval.
Forms
- medicinal products regulation
Related terms
See also
Commentary
Commonly used in the EU legal context to refer specifically to Regulation (EC) No 726/2004, it is essential to distinguish this regulation as it harmonizes medicinal product approval procedures and pharmacovigilance across member states.
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.