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The MS program in regulatory science is designed to prepare students for careers in the field of regulatory affairs. The program focuses on safety as a fundamental aspect of regulatory science, the application of regulations throughout the life cycle of medical products, and the compliance with regulations in the development, approval and marketing of medical products. The program incorporates a transdisciplinary approach to meet the unique needs of regulating bodies and the regulated industry. It encompasses coursework in clinical research, ethics, quality systems, legal aspects and global regulatory affairs in the regulatory field.
The Plan of Study is the required curriculum to complete the program.
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