Regulatory Management (MS)

专业介绍

USC Alfred E. Mann 药学院与制药科学学院的法规管理理学硕士（MS），要求至少 24 学分，常规学制 2 年。项目面向博士后科研人员与医疗专业人员，培养其在法规与临床研究领域的领导力，学会在团队环境中工作并管理生物医学产品开发与商业化相关的项目与人员。必修课程涵盖法规事务、质量保证、临床研究与项目管理。

The Master of Science in Regulatory Management prepares post-doctoral scientists and healthcare professionals for leadership in regulatory and clinical research. Students learn to work in a team-based environment, while managing projects and personnel related to biomedical product development and commercialization.   The degree is awarded upon completion of at least 24 units of formal course work. Required course work includes topics in regulatory affairs, quality assurance, clinical research, and project management. The program is designed for experienced professionals seeking to enhance their strategic and managerial skills within biomedical product development. Students gain the tools to lead regulatory teams and oversee complex product development programs. A study plan should be developed in consultation with graduate advisers before beginning the program. Recognizing the essentia