The regulation of clinical research is in itself a dynamic and emergent field. It brings together the science in which products drugs, devices, biologics and vaccines and treatment protocols are developed for improved global health care. Both the master s degree and graduate certificate programs prepare scientists and regulatory professionals to manage the key elements of the clinical research regulatory process. The rigorous curriculum focuses on regulatory strategy, regulatory guidance, legal and ethical issues, processes for product development and the business and political components of regulation in clinical research, all while reinforcing the science behind the methods.



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