Clinical Trial Information System (CTIS)

$49.00

In this course, you will learn all the important information about the CTIS, its timelines and user roles. You’ll also discover what training materials are available at European Medicines Agency website.

  • Course Type: Video Lessons
  • Language: English
  • Level: Advanced
  • Session: 2022
  • Time: 0 - 1 Hour
Category:

Course Breakdown

Section Time
Introduction 00:00:57
Clinical Trial Regulation 536/2014 00:03:42
The Keys Benefit of the CTR 536/2014 00:00:43
Clinical Trial Information System: What is it? 00:01:35
Timelines Implementation 00:01:07
CTIS Business Tool 00:00:39
CTIS Roles and Responsibilities 00:00:39
CTIS: Workspaces 00:03:11
Training Materials 00:08:32
CTIS Sponsor Handbook & Reference Materials 00:04:39

Exam and Certifications

  • Final Test – CTIS
  • Certification

Description

What I will learn?

We will explain what is the Clinical Trial Information System and why it’s considered a Regulation’s business tool. Moreover, we will look into the implementation timelines and system user roles and responsibilities.

Skills I will gain

  • Learn about the Clinical Trial Regulation 536/2014 and the key benefits
  • Learn critical timeline implementation
  • Understand the CTIS as a business tool
  • Expand your knowledge of the CTIS roles and responsibilities, workspaces, and additional training materials

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