Clinical Trials Regulation
/ˈklɪnɪkəl traɪəlz ˌrɛɡjʊˈleɪʃən/
Definitions
- (n.) A body of laws and regulations governing the conduct, authorization, and oversight of clinical trials to ensure safety, ethical standards, and scientific validity.
The Clinical Trials Regulation mandates strict protocols for obtaining informed consent from participants.
Forms
- clinical trials regulation
Related terms
See also
Commentary
The term typically refers to specific regulatory frameworks, such as the EU Clinical Trials Regulation, highlighting the intersection of law and medical research ethics.
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.