法规管理理学硕士

法规管理涉及参与生物医学产品开发的法规和法律要求的团队的领导，以及建立产品安全性和有效性所需的科学研究。法规管理科学硕士课程旨在为博士后科学家提供成为法规和临床研究领导者所需的知识和技能。完成至少24个单元的正式课程工作后，将授予监管管理理学硕士学位。学位要求包括与医疗产品开发，质量保证，临床研究和商业的监管方面有关的课程。在开始课程之前，学生应与研究生顾问协商制定具体的学习计划。
Regulatory management relates to the leadership of teams involved in the regulatory and legal requirements of biomedical product development to the scientific study needed to establish product safety and efficacy. The Master of Science in Regulatory Management program is designed to provide post-doctoral scientists with the knowledge and skills necessary to become leaders in regulatory and clinical research. A Masters of Science in Regulatory Management will be granted upon completion of at least 24 units of formal course work. Degree requirements include courses concerned with the regulatory aspects of medical product development, quality assurance, clinical research and business. Students should develop a specific plan of study in consultation with the graduate advisers before beginning the program.