Drug Adulteration Statutes
/ˈdrʌɡ əˌdʌltəˈreɪʃən ˈstætʃuːts/
Definitions
- (n.) Laws regulating the composition, quality, or purity of drugs to prevent contamination, misbranding, or harmful additives.
The drug adulteration statutes ensure that pharmaceuticals meet safety standards before reaching consumers.
Forms
- drug adulteration statutes
- drug adulteration statute
Related terms
See also
Commentary
Drug adulteration statutes often function alongside drug misbranding laws to comprehensively regulate pharmaceutical products' safety and labeling.
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.