Full course description
Good Clinical Practice (GCP) is the internationally recognized standard for the ethical and scientific conduct of clinical research involving human participants. This self-paced course provides an introduction to the principles, responsibilities, and requirements that guide clinical trials and research activities.
Throughout the course, you will explore the fundamentals of ethical research, participant protection, regulatory compliance, and quality management practices that support the credibility and reliability of clinical trial data. You will also learn the roles and responsibilities of research personnel and how GCP standards are applied throughout the lifecycle of a clinical study.
By completing this course, you will gain practical knowledge to help ensure research activities are conducted in accordance with established industry standards while protecting participant rights, safety, well-being, and confidentiality.
Course Skills:
• Foundations of ethical clinical research and participant protection
• Good Clinical Practice (GCP) principles and international standards
• Roles and responsibilities within clinical research teams
• Data quality, accuracy, and integrity requirements
• Regulatory compliance and research documentation practices
• Strategies for maintaining credibility and reliability in clinical trial outcomes
2h
100%
Digital Badge