×
Don't Miss Out!
Get your weekly Breakfast Briefing eNewsletter, filled with news, trends, and vital information from DIA!
Back to Agenda
Session 13: Reporting Adverse Events (AEs) During Clinical Trials
Session Chair(s)
Michael Hamrell, PhD, RAC
President
MORIAH Consultants, United States
- Definitions of Terms
- IND Safety Reports
- IND Annual Reports - Safety Information
- Discontinuation of Studies for Safety Reasons
Have an account?