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Introductory ICH GCP Course to Design International Clinical Trials

This course was previously called “Light ICH-GCP training – Design”. Learn about basic Good Clinical Practice principles and get a thorough introduction to the design of international clinical trials in ICH regions via this highly interactive, self-paced introductory e-learning course. Includes 2 interactive modules.

 65.00

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LEARNING OBJECTIVES

  • Principles of ICH GCP and the ICH GCP Addendum R2
  • Roles in clinical research
  • Abbreviations and terminology
  • Protocol development and content
  • Risk management
  • Selection of research sites and staff
  • Setting up quality assurance (DSMB and SOPs)
  • Monitoring and auditing
  • Creation of essential documents

 

DESCRIPTION

The Introductory ICH GCP course is the ideal introduction to Good Clinical Practice (GCP) and designing international clinical trials. It gives you the tools you need to develop protocols, draft essential documents, and select the right researchers and sites.

This course is tailored to the international ICH GCP regulatory framework and helps anyone involved in the design phase of clinical trials. It is an ideal introductory course for Ph.D. students, CRO and Sponsor Staff, Clinical Trial Assistants, and research staff.

  • Efficient and interactive online learning
  • Easy accessible via smartphone, tablet or desktop
  • Self-paced and modular

The course consists of 2 online training modules: Introduction and Design of a clinical trial. It represents a total workload of 2 hours. The modules are divided into chapters of 10 minutes and consist of the guidelines which apply to clinical trials, including the Declaration of Helsinki, and ICH GCP E6 Addendum R2. If you require additional knowledge for the execution of other phases of the trial, you can easily add these modules by upgrading to an Expert online ICH GCP training package.

After you have completed all components of the Introductory GCP e-learning course, you will receive a Certificate.

All training courses include one-year access to the online training. With our continuous learning model, we will keep you up-to-date with changing regulations and guidelines.

Enroll now to get started with the online learning modules on your smartphone, tablet, or desktop computer.

 

COURSE CONTENTS

Module 1: Introduction
Module 2: Design

Learn anytime, anywhere

Learn at your own pace on your smartphone, tablet or desktop. You will have one year of access to the training and resources so you can look up information even after you’ve completed the course.

Learn Continiously

Continuous Learning can both improve clinical research quality and ensure a motivated research team. You’ll benefit from better knowledge retention and reduced risks. We When a regulatory update is announced, we update the training modules and notify you, so that you can take the updated module and earn a new GCP certificate.

Earn your gcp certificate

With our courses, you can earn and maintain your vital industry-recognized certificate. In your GCP Passport, you can now see exactly which version of a training module you were most recently trained on. This documentation in combination with the changelog will inform auditors, managers, and inspectors of the associate’s compliance with current regulations.

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