Clinical research plays a crucial role in developing new medical treatments, ensuring their safety and effectiveness before reaching the public. This Clinical Research Fundamentals course provides a step-by-step understanding of how clinical trials are designed, conducted, and regulated. It covers essential topics such as trial phases, ethical considerations, Good Clinical Practice (GCP) guidelines, and global regulatory frameworks like FDA and ICH-GCP. Participants will also learn about the roles of investigators, sponsors, and ethics committees in the research process.
