RRT 300: Assessing Safety and Adverse Events

Content
1 module

Rating

Course Length
15 mins

Instructor
Advarra University

Price
$95.00

Description

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.

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 zzzz Advarra Completion Certificate (No Expire)

1.
RRT 300 Assessing Safety and Adverse Events
{{ vm.helper.t('courses.scorm') }}
 
Added 4 months ago, by Nancy
 
Added almost 2 years ago, by Bethany
 
Added about 2 years ago, by Andi
 
Added about 2 years ago, by Rachel
 
Added about 2 years ago, by Karlie
 
Added about 2 years ago, by Jan
 
Added about 2 years ago, by Craig
 
Added about 2 years ago, by Juli
 
Added about 2 years ago, by
 
Added over 2 years ago, by Patricia
The method of the presentation is great. Very clear and easy to follow.

Shopping Cart

Your cart is empty