The Association of Clinical Research Professionals

Identifying and Documenting Adverse Events: A Decision Making Process

Improve your understanding of adverse events (AEs) by working step-by-step through the definitions of the different types of AEs and reviewing the recording and reporting requirements of each. The speaker will provide a detailed review of AEs and requirements for assessment, documentation, recording, and reporting. Leave confident in your ability to effectively monitor AEs and ensure patient safety and data integrity.


This program is a recorded session from ACRP 2018