Overview
The purpose of this course is to allow users the ability to track documents and regulatory submissions that need to be made during the study life cycle. In this course, we will understand the process of how a CTMS Admin can configure our templates and document types within Configuration Management in order to enable the Document and Submission tracking process.
Recording of Global Education training sessions is strictly prohibited. Any attempts to record training will result in an immediate stoppage of training until recording is terminated.
Course Type
eLearning
Audience
Clinical Trial Administrators
Duration
21 min
Languages
English
Product
Configuration Management
Course Supplements
Course Outline - Configuring Document and Submission Tracking - ENG