Overview
Site Monitoring provides efficient monitoring of clinical studies with integrated workflows to improve the site monitor experience, aid proactive decision making, and reduce risk and costs to ultimately increase study performance, patient safety, and time to market for the drug or device.
This course focuses on how to manually add and conduct monitoring visits. Topics covered include:
- Accessing Site Monitoring
- Adding a Monitoring Visit
- Conducting a Monitoring Visit
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, Global Trial Managers, Information Technology Personnel, Programmers, Project Managers (Clinical), Reporting Specialists, Shippers, Site/User Administrators, Sponsor Personnel, Study Managers, System Administrators (Clinical)
Duration
15 min
Languages
English
Product
Medidata Site Monitoring
Course Supplements
SiteMonitoring_2017.1.0_VisitManagement_eLO_ENG_v1.0_Final.pdf