
Principle 1: Ethical Conduct and Participant Protection
Understand ICH E6(R3) Principle 1 and its six sub-principles that establish participant rights, safety, and well-being as the foundation of all clinical trial conduct.
The principle that governs everything else
Before there are protocols, before there are case report forms, before there is any discussion of monitoring or data management or regulatory submissions, there is a single foundational commitment that every clinical trial must honor: the people who participate matter more than the answers we seek.