Clinical Research & Trial Practical

Clinical research and clinical trials are fundamental to advancing healthcare, evaluating new interventions, and improving patient outcomes. This practical course provides participants with a structured introduction to the principles and processes involved in planning, conducting, documenting, and monitoring clinical research and clinical trials.

The course focuses on the practical aspects of clinical research, including research question development, study design, participant recruitment, informed consent, data collection, research documentation, ethical requirements, safety reporting, quality management, and basic clinical trial operations.

Participants will gain practical knowledge applicable to clinical research settings, academic institutions, hospitals, research organizations, and pharmaceutical or healthcare-related studies.