Includes a review of the historical context for the creation of the organizations that protect public health, including the Department of Health and Human Services and the Food and Drug Administration. The course challenges students to become critical thinkers and approach cases from a leadership perspective, considering how to integrate responsibility into organizational culture. Quality Systems and Clinical Research track course. Students will gain and apply skills in developing and leading projects that create value in any area, but with specific focus on improving quality, service, and regulatory compliance. APPLY NOW The online Juris Master is a 30-credit-hour master’s in law that can be completed on a part-time basis. This course is designed to provide an overview of the drug development process with an emphasis on the conduct of clinical trials. Two or three years of work experience in the field can be substituted if an applicant holds a degree in area other than pharmacy or life sciences. The Master's in Regulatory Compliance requires the completion of 11 courses. This course explores quality standards and compliance regulations governing the manufacture and quality control testing of products with a focus on the laboratory setting.

Working in Regulatory Affairs: Careers, Salaries, and Trends, The Evolution of Food Safety: From Barcode to Blockchain, Regulatory Affairs for Drugs, Biologics, and Medical Devices, Biopharmaceutical International Regulatory Affairs, Biopharmaceutical Domestic Regulatory Affairs, Nonclinical Regulation of Biomedical Products, Quality Assurance in Biomedical Product Regulation, 360 Huntington Ave., Boston, Massachusetts 02115, 5 Media Literacy Activities for College Students, Join Us at Northeastern’s Virtual Graduate Open House, International out-of-country application complete (start date: September 14, 2020), International in-country application complete (start date: September 14, 2020), Domestic application complete (first half start: September 14, 2020), Domestic application complete (second half start: October 26, 2020), International out-of-country application complete (start date: January 11, 2021), International in-country application complete (start date: January 11, 2021), Domestic application complete (first half start: January 11, 2021), Domestic application complete (second half start: February 22, 2021), International out-of-country application complete (start date: April 12, 2021), International in-country application complete (start date: April 12, 2021), Domestic application complete (first half start: April 12, 2021), Domestic application complete (second half start: May 24, 2021), International out-of-country application complete (start date: July 12, 2021), International in-country application complete (start date: July 12, 2021), Domestic application complete (start date: July 12, 2021).
"Experienced regulatory professionals are in demand.

The course describes compliance healthcare enforcement authorities, such as Medicare and Medicaid auditors (e.g., Recovery Auditors, UPIC’s) and current key healthcare fraud initiatives.
Upon completion, students will have the knowledge and basic skills to pursue a position coordinating clinical trials at an investigative site or an operational position within a pharmaceutical company.

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