Content
1 module
Rating
Course length
15 mins
Instructor
Miranda Schramm
Price
$0 - 95 USD
Description
This course covers the guidelines for assessing the safety and well-being of study participants set in accordance with Good Clinical Practice (GCP).
Objectives
By the end of this course, learners will be able to:
- Define and identify adverse events in a trial
- Understand why and how to document and communicate adverse events
- Determine whether it is safe for a participant to continue in a study after experiencing an adverse event
- Respond to an outside safety report (OSR)
Certificate
By completing/passing this course, you will attain the certificate Advarra Completion Certificate
1.
RRT 300 Assessing Safety and Adverse Events
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