This course provides a comprehensive introduction to the pharmaceutical and clinical research industry, its history, and key milestones. Learners will explore the roles and responsibilities of stakeholders, ethical foundations, and global regulatory frameworks governing clinical trials. Core principles of Good Clinical Practice (GCP) are emphasized, along with essential trial processes and documentation. The module also covers emerging technologies in trial management and the importance of safety reporting. Designed as a foundation, it prepares learners for deeper study in advanced clinical research concepts and practices.