RRT 310: Clinical Trial Monitoring

5 modules


Course Length
15 mins

Advarra University



During a clinical trial, the sponsor will sometimes send a representative known as a monitor to your site to review the study’s progress. This course will discuss how to plan and conduct those monitoring visits. 

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:

  • Understand what a clinical trial monitor entails
  • Understand the role the monitors play
  • Be able to report on protocol deviations
  • Understand how to prepare for and conduct monitor visits


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

Introduction to Clinical Trial Monitoring
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Reporting Protocol Deviations
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Preparing for Monitor Visits
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Conducting Monitor Visits
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Added about 1 month ago, by Pamela
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Question 9 is blank - no question exists
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There was no question for #9.
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Added 5 months ago, by Patricia
The method of the presentation is great. Very clear and easy to follow.

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