In this video, we cover:
- The phases of the preclinical and clinical development and approval processes for new medicines,
- The bases for the major regulations guiding the development of new medicines,
- The responsibilities of investigators in clinical trials and the impact of misconduct on patient care,
- The enrollment of an ethnically-diverse population into clinical trials of new medicines and why inclusion diversity is important.
Moderator: Elbert Nelson, MD
Presenter: James H. Powell, MD