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.

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This program is a recorded session from ACRP 2018