The Good Clinical Research Regulation Training (GCRRP) course provides a comprehensive framework for equipping research regulators, investigators, and research teams with the knowledge and skills necessary to uphold research integrity.
The course comprises 20 topics categorized into three thematic areas:
- Research ethics dealing with principles and guidelines for ethical research conduct.
- Legal and human rights in research considering issues related to laws, policies, and human rights in research.
- Research misconduct and regulatory oversight that deals with identifying, managing, and preventing research misconduct, offences, and non-compliance.
This course is designed to build on participants' existing knowledge, it is structured to relate directly to the real world experiences in research oversight and clinical investigations.
- Teacher: KGS Admin