Using myMedidata eConsent in Your Clinical Trial

Courses

Prerequisites

Getting Started: Using myMedidata in Your Clinical Trial

Overview

This course is intended for Site Users and Administrators and provides a thorough understanding of how to support or manage myMedidata studies to carry out common tasks and responsibilities.

For example, you will learn how:

- Patients Consent with myMedidata eConsent
- Consent Workflow with Video Visit Required
- Consent Workflow for No Video Visit
- Patients Sign the Informed Consent Form (ICF)
- Clinicians Countersign the Informed Consent Form (ICF)

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

Clinicians, Site Personnel, Site/User Administrators

Duration

15 min

Languages

chinese, English, Japanese, Korean

Product

myMedidata

Course Supplements

Using myMedidata eConsent in Your Clinical Trial - Course Outline - ENG

Training Alerts

March 3, 2023

February 2023 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.

Medidata Academy Confidentiality Agreement

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By continuing with the registration process, you are agreeing to the Medidata Academy Confidentiality Agreement.

I have read and agree to the terms for registration.