临床管理事务理学硕士（MSCRA）提供了临床试验领域的全面研究生课程以及与开发和执行临床试验相关的联邦法规。监管事务硕士课程基于讲授性讲座，案例研究以及与联邦政府法规以及临床试验研究的监测和协调相关的综合文章和文章。该法规事务研究生课程将使学生具有该领域的全面知识，开发和实施适当的协议和文件，以及了解数据管理和临床试验研究行业。
The Master of Science in Clinical Regulatory Affairs (MSCRA) provides a comprehensive program of graduate study in the field of clinical trials and the federal regulations associated with developing and performing clinical trials. The master's in regulatory affairs program is based on didactic lectures, case studies, and comprehensive texts and articles associated with federal government regulations and clinical trial research monitoring and coordinating. This regulatory affairs graduate program will allow the student to have a comprehensive knowledge of the field, develop and implement appropriate protocols and documents, as well as understand data management and the clinical trials research industry. The world of clinical drug trials is complex and fascinating. As an employee in this field, you'll need an understanding of the federal regulations for approving new drugs or medical devices as well as a fundamental knowledge of human rights obligations and adverse events. From clinical trial monitoring to data collection to manufacturing, this is a field with a deep mix of science and social matters. By earning a Master of Science in Clinical Regulatory Affairs (MSCRA), you'll gain a comprehensive knowledge of the field, develop and implement appropriate protocols and documents, and understand data management and the clinical trial research industry. Prepare for a future as a health professional through evidence-based research and clinical skill development with a curriculum that emphasizes prevention and integrative approaches to health care. National University prepares students with health sciences degrees for rewarding careers in the health care industry. You'll gain the knowledge, skills, and values to advance in your profession, meet society's health care delivery demands, and work in settings with diverse patients, families, and communities.