Program overview
Admission Requirements
Intakes

Last updated on 2026-07-31

Program overview

Program overview

Advance your career in Toronto with a Master of Science in Regulatory Affairs from Northeastern University. This program is designed to equip you with the expertise needed in global compliance, product approvals, and regulatory strategy specifically for the healthcare and life sciences sectors. As the demand for regulatory affairs professionals continues to grow, this unique graduate degree will deepen your understanding of the compliance requirements necessary for the development, marketing approval, and utilization of highly regulated products, including food, drugs, biologics, and medical devices.

Program structure

The Master of Science in Regulatory Affairs program at Northeastern University offers a comprehensive structure that prepares students for a successful career in regulatory affairs. The program is designed to be flexible, allowing students to choose between part-time and full-time study options. The program length is 12 to 18 months, providing a thorough exploration of the regulatory landscape.

Key features of the program structure include:

  • Entry terms available in Fall and Spring.
  • On-ground learning format in Toronto.
  • Opportunity to participate in a co-op program or integrative experiential learning.
  • Focus on one of five unique concentrations within the field of global regulatory affairs.

Featured Experiences

The Master of Science in Regulatory Affairs program offers a variety of unique experiences that enhance learning and professional development:

  • Students can engage in integrative experiential learning opportunities that provide real-world experience.
  • The co-op program allows students to gain hands-on experience in the field, working with industry leaders.
  • Access to a global network of alumni from renowned companies such as Pfizer, Novartis, and Merck.
  • Participation in a monthly lecture series, ALERT, featuring regulatory professionals discussing evolving global regulatory frameworks and industry trends.
  • Focus on biomedical product regulations applicable to commercialization in Canada.

Career Options

Graduates of the Master of Science in Regulatory Affairs program can pursue a variety of career paths in Canada. Here are some potential job options:

  • Regulatory Affairs Specialist: Responsible for ensuring that products meet all regulations and standards before they can be marketed.
  • Compliance Manager: Oversees compliance with regulatory requirements and develops policies to ensure adherence to laws and regulations.
  • Clinical Research Associate: Manages clinical trials and ensures that they comply with regulatory standards and protocols.
  • Quality Assurance Manager: Ensures that products meet quality standards and regulatory requirements throughout the production process.
  • Product Development Manager: Guides the development of new products, ensuring they meet regulatory requirements from conception to market launch.

 

DISCLAIMER: The information above is subject to change. For the latest updates, please contact LOA Portal's advisors.

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