Creation of an informed consent form can be a time-consuming process, laden with unexpected delays and protracted negotiations between sponsors, institutional review boards (IRBs), and other stakeholders in clinical research. This session will help attendees to better understand the life cycle of an informed consent form as it moves from a global study template to a site-specific document that is used to share critical information with study participants, and to learn strategies for positioning sites with strong rationale for making critical revisions.

CEU: 1.00 ACRP

Speaker:

Dawn Pedinelli, Senior Manager, Astellas Pharma

Watch a Sneak Peek into the Session Content: