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 Client Division level. Topics covered include:
- Configuration of Visit Types and Conduct Methods
- Configuration of Visit Activities and Questions
- Configuration of Risk Categories
- Configuration of Visit Matrix
- Configuration of Visit Report Templates
- Configuration of Visit Letter Templates
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, System Administrators (Clinical)
Duration
21 min
Languages
English
Product
Medidata Site Monitoring
Course Supplements
eLearning Outline - Medidata Site Monitoring Client Division Level Settings (ENG)