Good Clinical Practice (GCP) is a set of international ethical and scientific quality standards that guide the design, conduct, and reporting of clinical trials. These guidelines ensure that the rights, safety, and well-being of trial participants are protected while also ensuring that the data collected is credible and reliable. GCP applies to all aspects of clinical research, including the roles of researchers, sponsors, and regulatory authorities. By adhering to GCP, organizations can ensure compliance with regulatory requirements and maintain the integrity of the research process, ultimately contributing to the development of safe and effective medications and treatments.