Clinical Trials: Regulatory, Management, and Operational Aspects - Major of the Master's Program in the Health Industry

The Master’s program aims to equip students with the theoretical and practical tools needed to properly plan, conduct, and manage a clinical trial. This is achieved through learning about the methodology of clinical drug trials, study protocol design, subject enrollment methods, evaluation of treatment efficacy and tolerability, and ethical considerations. Furthermore, given the ongoing regulatory changes in this field, the Master’s program also aims to address updates to national legislation governing the conduct of studies, as well as the most relevant current issues and research developments.

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