Medidata Site Monitoring: Submit, Review, and Approve Visits

Courses

Prerequisites

Medidata Site Monitoring: Visit Management

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 submitting, reviewing, and approving the visit reports. Topics covered include:

Preview and Submit Visit Reports
Review and Comment on Visit Reports
Reject and Resubmit Visit Reports
Approve Visit Reports

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, Monitors, Site Personnel, Site/User Administrators, Study Managers, System Administrators (Clinical)

Duration

10 min

Languages

English

Product

Medidata Site Monitoring

Course Supplements

eLearning Outline - Medidata Site Monitoring Submit Review and Approve Visit Reports (ENG).pdf

Training Alerts

August 5, 2024

July 2024 Medidata Global Education Monthly Course Digest

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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