This session will review various myths, fine points, and current topics related to Human Subjects Protection (HSP) and Good Clinical Practice (GCP) in clinical trial administration and operations.

Using a thought-provoking format, we will determine what is true or false, define and elaborate on best practices, and discover answers with references for a deeper dive. When myths are identified, we will talk about how myths get started and how to avoid creating or propagating them.

We will evaluate compliance questions, common interpretations, and site processes against requirements, rules, and regulations to recommend solutions for issues of all kinds and complexities.

MODERATOR

Jennifer Peterson - Director, Head of Clinical Quality - M3 Wake Research

SPEAKER

Jeanna Julo - Quality Improvement & Compliance Officer - University of California, San Francisco