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 explores the new features and enhancements added in the 2018.3.0 release of Site Monitoring, including:
- Reference Data for Visit Life Cycle
- Visit Report and Approval Notifications
- Editable Monitoring Visit Letters
- Visit Settings Enhancements
- Issue Creation Enhancements for Visits
- Letter and Report Template Improvements
- Data Placeholder Enhancements
- End Triggers for Visit Schedules
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, Data Entry Personnel, Monitors, Site Personnel, Site/User Administrators, Study Managers, System Administrators (Clinical)
Duration
5 min
Languages
English
Product
Medidata Site Monitoring
Course Supplements
eLearning Outline - Medidata Site Monitoring: 2018.3.0 Release Training (ENG)