This is the AstraZeneca Adverse Event Training Module for 3rd Party Vendors. If you have a contract with AstraZeneca to undertake activities on our behalf you may receive information about Adverse Events (AEs) associated with our medicines from Healthcare Professionals and/or members of the public. This module will provide you with the necessary training and processes to meet the regulatory requirements for Adverse Event reporting. The training module will be followed by a short quiz to check your understanding of the requirements, the pass mark is 80%.
Format : Module and Quiz
Time to Complete : 30
Released: 18/11/2015
Expires: 31/12/2035
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