Regulatory Affairs

Students Overview

Below is a look at where our Regulatory Affairs alumni work, the positions they hold, and the skills they bring to their organization.

 

  • Where They Work

    • Shire
    • Pfizer
    • Medtronic
    • Biogen
    • Teva Pharmaceuticals
  • What They Do

    • Legal
    • Research
    • Quality Assurance
    • Operations
    • Healthcare Services
  • What They're Skilled At

    • Regulatory Affairs
    • Pharmaceutical Industry
    • U.S. Food and Drug Administration
    • Clinical Trials
    • Standard Operating Procedure (SOP)

 

Learn more about Northeastern Alumni on Linkedin.

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Graduate Certificate in Quality Assurance in Biomedical Product Regulation-Silicon Valley

Submitted by Rebecca on Wed, 05/01/2019 - 11:04

The Graduate Certificate in Quality Assurance for Biomedical Products provides an in-depth knowledge of the global regulatory and compliance requirements for the development, marketing approval and clinical utilization of biomedical products in today’s dynamic global healthcare environment.

Graduate Certificate in Quality Assurance in Biomedical Product Regulation - Online

Submitted by neuglobal on Sun, 04/28/2019 - 17:03

The Graduate Certificate in Quality Assurance for Biomedical Products provides an in-depth knowledge of the global regulatory and compliance requirements for the development, marketing approval and clinical utilization of biomedical products in today’s dynamic global healthcare environment.

Graduate Certificate in Quality Assurance in Biomedical Product Regulation-Boston

Submitted by Rebecca on Thu, 04/25/2019 - 14:05

The Graduate Certificate in Quality Assurance for Biomedical Products provides an in-depth knowledge of the global regulatory and compliance requirements for the development, marketing approval and clinical utilization of biomedical products in today’s dynamic global healthcare environment.

Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices — Silicon Valley

Submitted by neuglobal on Wed, 11/22/2017 - 11:12

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.

Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices — Toronto

Submitted by neuglobal on Fri, 08/12/2016 - 18:10

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.

Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices — Online

Submitted by a.delorenzo@neu.edu on Fri, 07/15/2016 - 16:33

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.