05/07/2025
In the ever changing world of clinical research, staying up to date with the latest guidelines and best practices is crucial. Our ICH E6(R3) Good Clinical Practice Training is designed for busy professionals who want to deepen their knowledge on GCP to help ensure they meet the highest standards of quality, safety, and compliance. Whether you're just starting in the industry or have years of experience, the revisions are significant enough that everyone will benefit from taking the full training. We highly recommend pairing with our Overview of ICH E8(R1): General Considerations for Clinical Studies Guideline course, as ICH E8(R1) provides the essential foundation to ICH E6(R3). Bundle options are available for those looking for a streamlined learning experience.
Why Choose Our Training?
Expert Guidance: Our course is developed by industry experts with years of experience in clinical trials. You'll get insights into the most current practices, guidelines, and computerized systems in clinical research.
Gain Practical Knowledge: Learn how to apply GCP principles and ICH E6(R3) guidelines to your organization. We cover critical topics like stakeholder responsibilities, computerized systems, and risk management.
Learn at Your Own Pace: Our flexible, self-paced online course allows you to learn on your own schedule. Access the training anytime, anywhere, and complete it at a pace that fits into your busy schedule.
Comprehensive and Interactive: The training includes knowledge chunked into easier to digest modules, knowledge checks after each content area, and real life case scenarios to help reinforce your understanding of key concepts learned throughout the training. The computer based training includes interactive elements to engage your interest in the topics.
Certification of Completion: Upon finishing the course, you'll receive a certificate that demonstrates your commitment to maintaining high standards in clinical research. This certification can boost your credibility and career opportunities in the clinical research field.
What You'll Learn:
Principles of Good Clinical Practice and their role in safeguarding participants and data integrity.
The latest updates from ICH E6(R3) guidelines, including Quality by Design, Critical to Quality factors, risk management, and the latest guidance on computerized systems.
Strategies for proactive inspection readiness and a deeper understanding of common areas of interest in an inspection.
Why It Matters:
By completing this training, you’ll be better equipped to manage trials efficiently, reduce risks, and improve quality. Completing GCP training will enhance your contributions to your organization and also refine your skills and expertise, strengthening your professional credibility and helping you stand out in the competitive job market.
Ready to Get Started?
Purchase our Clinical Pathways’ Good Clinical Practice Training: ICH E6(R3) today HERE and our Overview of ICH E8(R1): General Considerations for Clinical Studies Guideline HERE. Whether you're a beginner or a seasoned clinical research professional, adequate and recent GCP training is essential.
Bundles, enterprise options and webinars are also available. Contact us at info@clinicalpathwaysresearch.com for more information.