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Master of Science in Regulatory Affairs - Clinical Research Regulatory Affairs (Concentration) Northeastern University - Toronto Campus Northeastern University - Toronto Campus, Canada

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CAD 28280

Annual Tuition Fee

!
*Subject to change and other fees
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CAD 75 Waived

Application Fee

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21 months

Duration

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6.5

IELTS

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79

TOEFL

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60%

Min GPA

Program Overview

The Master of Science in Regulatory Affairs program is designed to produce graduates who are highly qualified to manage global regulatory processes for companies innovating and developing cutting-edge products in healthcare and food safety.


The ongoing global convergence of regulatory science, technology-driven regulatory decision making, formation of public policies, and ever-changing regulations are driving demand for regulatory affairs professionals who can help companies effectively bring highly regulated 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. This unique graduate degree is designed to deepen your understanding of the global compliance requirements for the development, marketing approval, and utilization of highly regulated products, including food, drugs, biologics, and medical devices.


Regulatory affairs courses within this program will provide you with the integrated knowledge and broad perspectives you need to effectively manage the appropriate industry-specific regulatory process throughout a product’s life cycle. From discovery to commercialization, this regulatory affairs master’s degree will cover the steps that are required to bring a highly regulated product to market, both in the U.S. and around the globe.


Northeastern’s MS in Regulatory Affairs offers students the opportunity to meet their career goals and gain deeper experience in key areas of regulatory affairs—such as operational and strategic regulatory affairs, clinical regulatory affairs, new gene therapies, cybersecurity of medical devices, quality assurance in biopharmaceutical product formulation, validation of medical device commercialization, food safety, and regulatory compliance—by focusing their education in one of five unique concentrations that span the entire discipline.
 

Concentration: Clinical Research Regulatory Affairs

Provide practical knowledge of regulatory requirements and methodologies for clinical human and animal research to support biomedical product development.

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Additional Information

Program Level Master's Degree

College/University Processing Time 42 Days

Program Format Full-Time

Post-Graduation Work Permit (PGWP) work permit

Program Intake

Open

Sep 2025

Closed

Jan 2024, Jan 2025, Sep 2024

General Admission Requirement

  • IELTS
    • Minimum Overall Score - 6.5 - With No Band Less Than - 6
  • TOEFL
    • Minimum Overall Score - 79.0  Minimum Writing - 20.0  
  • PTE
    • Minimum Overall Score - 53
  • DUOLINGO
    • Minimum Overall Score - 105.0  

Academic Requirement

  • Minimum Level of Education Required: To be accepted into this program, applicants must have a Bachelor’s degree from an accredited college or university.

6.5 IELTS Score
79 TOEFL Score Minimum Overall Score
53 PTE Score Minimum Overall Score
105 Duolingo Minimum Overall Score
60% CGPA Minimum Overall Score

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Tuition Fee

The values given below are estimated figures, excluding extra charges like material fee, student activity fees, athletic fees, health care, etc., for courses. To know more, please visit the Programs page.

Average Tuition Fee Per Year

28280

Tuition Fee
(CAD)

CAD 75 Waived

Application Fee
(CAD)

12000 Per year

Average Cost of Living
(CAD)

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The living costs include the total expenses per month, covering accommodation, public transportation, utilities (electricity, internet), books and groceries.

Check program website for more information about funding options.

Scholarships

Merit-based scholarships are available, ranging between 25%-50% off on the program's tuition cost.

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