Rave CTMS: Using Document and Submission Tracking
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 users have access to actionable information which helps ensure that documents are available, and that submissions are made to the regulatory authorities on time.
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.
Clinical Trial Administrators, Monitors, Study Managers
Course Outline - Rave CTMS: Using Document and Submission Tracking - ENG