The Adverse Events and Product Complaints Course
The Adverse Events and Product Complaints Course is a 1 day course.
Cost: $450
Are you curious about the IRMS AE
module’s ability to capture and report on your adverse events? This
course is designed for IRMS users who will be setting up and entering
Adverse Events using the AE module. We will discuss starting the
AE tables and proper setup; Adverse Events screen which includes
the Demographic Tab, Narrative Tab, Medications Tab, Adverse Events
Tab, Labs & History Tab, Comments Tab, and the Due Dates Tab. We
will go over the AE Worksheet and 3500A form, as well as setting
User Preferences and Required Fields for Adverse Events, the AE
Crosslink feature, and the new Case Correspondence (tickler file)
functionality. We will also discuss AE Reporting and Query.
Would you like to use IRMS for efficient
complaint tracking and reporting? IRMS users who will be setting
up and entering Product Complaints will be interested in this class.
IRMS Product Complaint module allows you to enter and track complaints
regarding specific products. We will go over the Product Complaint
tables setup, as well as the Product Complaint screen which includes
the General Info Tab, Drug Detail Tab, General Activity Tab, and
Other Activity Tab. We will also discuss the Crosslink and Case
Correspondence features, and Product Complaint Reporting and Query
Register For a Class