Medidata Site Monitoring: Study Environment Level Settings

Prerequisites

Medidata Site Monitoring: Client Division Level Settings

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 configure Site Monitoring settings at the Study environment level. Topics covered include:

• Access Study Environment Level Settings
• Copy Client Division Level Settings
• Create Visit Schedules
• Configure Study Sites Settings
• Configure Report Settings

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 Supplements

eLearning Outline - Medidata Site Monitoring: Study Environment Level Settings (ENG)