Data Surveillance: Configure Data for Data Surveillance

Courses

Prerequisites

Introduction to Clinical Data Studio

Overview

In this course, you will learn about:

What is Data Surveillance and its Purpose and
How to Configure Data for various capabilities within Data Surveillance

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

Data Managers, Functional Managers, Programmers, Project Managers (Clinical), Study Managers

Duration

67 min

Product

Clinical Data Studio

Course Supplements

Course Outline - Data Surveillance: Configure Data for Data Surveillance - ENG

Training Alerts

August 4, 2026

July 2026 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

PLEASE READ THIS AGREEMENT CAREFULLY. REGISTERING FOR ANY MEDIDATA ACADEMY COURSE AND/OR TAKING ANY CERTIFICATION EXAM INDICATES YOUR ACKNOWLEDGMENT THAT YOU HAVE READ THIS AGREEMENT AND ACCEPT ITS TERMS AND CONDITIONS. IF YOU DO NOT AGREE TO THESE TERMS, DO NOT REGISTER.

You agree, in consideration for, and as a prerequisite to, taking any Medidata Academy course and/or exam, to the following terms and conditions. If you are not in agreement with the following, you will not be able to take Medidata Academy courses or exams. Click here to read the Medidata Academy Confidentiality Agreement.

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.

Study Experience Overview

Clinical Trial Financial Management

CTMS

eTMF

Grants Manager

Protocol Optimization

Site Payments

Study Feasibility

Synthetic Control Arm®

Patient Experience Overview

eCOA

Consent

Decentralized Clinical Trials

Medidata Diversity Program

myMedidata

myMedidata Registries

Patient Payments

Sensors

Data Experience Overview

Adjudicate

Clinical Data Studio

Coder+

Companion

Designer

Health Record Connect

Imaging

Link

Rave

Rave Lite

RTSM

Safety Gateway

Site Cloud: End of Study

Surgical Planning

Targeted SDV

Professional Services Overview

Customer Success

Strategy and Transformation Consulting

Study Configuration Services

Clinical Trial Financial Management

Grants Manager

Integrated Evidence

Medidata Diversity Program

Study Feasibility

Patient Insights Program

Site Insights Program

Synthetic Control Arm®

Consent

Designer

Protocol Optimization

Study Feasibility

Adjudicate

Clinical Data Studio

Coder+

Companion

CTMS

Decentralized Clinical Trials

eTMF

Health Record Connect

Imaging

Link

eCOA

myMedidata

Patient Payments

Rave

Rave Lite

RTSM

Safety Gateway

Sensors

Site Payments

Targeted SDV

myMedidata Registries

Site Cloud: End of Study

Surgical Planning

CRO Partners

Partner Program

Find a Partner

Partner Portal

Emerging & Mid-sized Biopharma

Large Biopharma

MedTech