Clinical trial management involves the planning, execution, and monitoring of clinical trials to test new drugs, treatments, or medical devices. This process ensures that trials are conducted according to regulatory standards and ethical guidelines, safeguarding the rights and well-being of participants. Key components of clinical trial management include participant recruitment, data collection, and analysis. Effective management helps streamline operations, maintain compliance with FDA regulations, and ensure accurate reporting of results. This ultimately contributes to the development of safe and effective medical interventions for patients.