Ensuring Clinical Research Quality & Patient Safety In-house Training

Part of Responsible Conduct of Research (RCR) series:

Overview

This course provides an essential overview of Good Clinical Practice (GCP) principles, ensuring that participants understand the ethical and regulatory foundations of conducting clinical research. Topics covered include research integrity, participant safety, informed consent, data management, and compliance with international and federal guidelines.

This course is part of our GxP training (Good x Practice) course collection, which features a variety of topic areas to ensure you comply with the most recent quality guidelines.

Benefits of attending

• Understand the main principles of Good Clinical Practice (GCP)
• Ensure ethical conduct and participant safety
• Know the importance of data integrity in clinical trials

Who should attend?

• Clinical research professionals, including clinical research associates, investigators, and study coordinators
• Medical writers, regulatory writers, and publication professionals
• Quality assurance specialists and compliance officers in pharmaceutical and clinical research organisations
• Anyone involved in clinical trial documentation, regulatory submissions, or scientific publications seeking to improve their understanding of good practices and ethical guidelines