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ICH Good Clinical Practice (GCP) Refresher (Including E6 R3)
Use discount code GCPHALFPRICE for 50% off the course. Offer expires 26th March 2025.
Introducing our brand new, interactive, and engaging online GCP refresher training course, designed for individuals who have completed a full GCP course within the last two years. This course refreshes your previous knowledge while incorporating the latest ICH GCP E6 Revision 3 guidance, released on 6th January 2025, reflecting the most recent changes in the GCP framework to ensure compliance with global standards for clinical trials.
This comprehensive refresher training is perfect for those involved in clinical research who want to stay current with the latest regulatory updates and best practices. Participants will receive official GCP certification, recognised by sponsors and CROs worldwide. Created by subject matter experts with over 35 years of experience in clinical research, this course includes improved knowledge checks and interactive elements to enhance engagement and effectiveness in the learning process.
As a participant, you are responsible for ensuring your knowledge and compliance with GCP standards. Please note that while this course meets the training requirements set forth by Transcelerate Biopharma Inc., we cannot guarantee your compliance if you previously completed GCP training with another provider. This refresher course is ideal for helping you maintain compliance and stay informed about the latest developments in clinical trial standards.
The Faculty of Pharmaceutical Medicine has approved this online GCP training course for CPD points.
CPD Points Available: 4
Learning Objectives in the GCP Refresher Training
- Understand Key Changes in ICH GCP E6 R3
Gain a comprehensive understanding of the new principles, updates, and roles in the ICH GCP E6 R3 guidelines and their impact on clinical trials. - Prepare for Implementing ICH GCP E6 R3
Learn how to adapt and implement the updated GCP standards in your role, ensuring full compliance with the latest guidelines and enhancing trial conduct. - Navigate Evolving Roles and Responsibilities
Understand the updated roles and responsibilities for investigators, sponsors, and key stakeholders as outlined in the E6 R3 guidance. - Ensure Effective Risk Management
Develop skills to assess and manage risks in clinical trials using updated GCP risk-based approaches to ensure safety and compliance.<p”> - Promote Data Integrity, Quality, and Monitoring
Explore strategies for maintaining data integrity, ensuring high-quality practices, and applying effective monitoring techniques to enhance oversight and compliance in clinical research.
These objectives ensure that participants not only understand the theoretical aspects of ICH GCP E6 R3 but also how to practically apply the principles to their work in clinical research.
