Monitoring in clinical trials

Clinical monitoring is the oversight and administrative efforts that monitor a participant's health and efficacy of the treatment during a clinical trial. Both independent and government-run grant-funding agencies, such as the National Institutes of Health (NIH) and the World Health Organization (WHO), require data and safety monitoring protocols for Phase I and II clinical trials conforming to their standards.

Source: Wikipedia — Monitoring in clinical trials (CC BY-SA 4.0)

Monitoring in clinical trials

Clinical monitoring is the oversight and administrative efforts that monitor a participant's health and efficacy of the treatment during a clinical trial. Both independent and government-run grant-funding agencies, such as the National Institutes of Health (NIH) and the World Health Organization (WHO), require data and safety monitoring protocols for Phase I and II clinical trials conforming to their standards.

Source: Wikipedia "Monitoring in clinical trials" · CC BY-SA 4.0

Share this article: X · Bluesky
Privacy Policy