Clinical Research Protocol
/ˈklɪnɪkəl rɪˈsɜːrtʃ ˈproʊtəˌkɒl/
Definitions
- (n.) A detailed plan approved by regulatory authorities that outlines the methodology, objectives, and statistical considerations for conducting clinical research involving human subjects.
The clinical research protocol must be followed strictly to ensure patient safety and data integrity.
Forms
- clinical research protocol
- clinical research protocols
Related terms
See also
Commentary
Clinical research protocols are critical legal documents that must comply with ethical standards and regulatory requirements to ensure lawful and ethical conduct of clinical studies.
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.