药物，生物制品和医疗设备监管事务理学硕士（硅谷）

药物，生物制品和医疗器械监管事务理学硕士课程旨在培养具备高素质的毕业生，以管理创新和开发尖端科学和医学产品的公司的监管流程。推动对法规事务专业人员的需求，这些专业人员可以帮助公司有效地将医疗产品推向市场。为了使您能够有效地管理监管活动，东北大学专业研究学院提供了药品，生物制品和医疗器械监管事务理学硕士学位。这个独特的研究生学位旨在加深您对当前法规及其在药物，生物制剂和医疗器械产品的开发和商业化中的实际应用的理解。该计划中的法规事务课程将为您提供所需的综合知识和广泛见解有效地管理法规流程。从发现到商业化，该
The Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices program is designed to produce graduates who are highly qualified to manage the regulatory process for companies innovating and developing cutting edge products in science and medicine.Ever-changing laws and regulations are driving demand for regulatory affairs professionals who can help companies effectively bring medical products to market. To prepare you to effectively manage regulatory activities, Northeastern University's College of Professional Studies offers the Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices. This unique graduate degree is designed to deepen your understanding of current regulations and their practical application in the development and commercialization of drugs, biologics, and medical device products.Regulatory affairs courses within this program will provide you with the integrated knowledge and broad perspectives you need to effectively manage the regulatory process. From discovery to commercialization, this regulatory affairs master's degree will cover the steps that are required to bring a medical product to market, both in the U.S. and around the globe.