Medidata Site Monitoring: Study Environment Level Settings

Courses

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 Type

eLearning

Audience

Clinical Trial Administrators, Site/User Administrators, Study Managers, System Administrators (Clinical)

Duration

15 min

Languages

English

Product

Edge Strategic Monitoring

Course Supplements

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

Training Alerts

April 27, 2018

Medidata Academy announces new Site Monitoring: Study Environment Level Settings eLearning!

Payment Method

If paying by Purchase Order (PO), please e-mail an authorized PO to invoicing@mdsol.com. You will be invoiced for the full amount of the training class with net 30 terms in the month following training. PO must be received 5 business days prior to the start of the class to guarantee enrollment.

Existing Agreement
To schedule a public training utilizing an existing agreement, please contact your Medidata Project Manager.

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