RRT 300: Assessing Safety and Adverse Events

6 modules


Course Length
15 mins

Advarra University



This course covers the guidelines for assessing the safety and well-being of study participants set in accordance with Good Clinical Practice (GCP).

Attendance at this program has been approved for 0.50 contact hours of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 0.50 hours of CE credit.


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)


By completing/passing this course, you will attain the certificate Advarra Completion Certificate (No Expire)

Assessing and Recording Adverse Events
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The MedWatch Report
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Participant Safety
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Reporting Adverse Events
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Safety Events and Study Design
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The method of the presentation is great. Very clear and easy to follow.
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