Medidata Site Monitoring: 2018.3.0 Release Training

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)

How To Register

Select the date and location to proceed to the registration and payment form.