Pharmaceutical Regulatory Affairs & Quality Operations (RAQ)(Online)

Program overview

Focus your career by specializing in the Pharmaceutical Regulatory Affairs & Quality Operations (RAQ) program, a one-year graduate certificate offered online. This program provides a fundamental understanding of regulatory affairs and quality operations, preparing you for a career in drug or medical regulations and quality assurance roles. You will study regulatory compliance both in Canada and internationally. The first semester covers the basics, while the second semester delves deeper into regulation and quality operations. An optional work term is available, allowing you to gain practical experience in your field.

Program structure

The Pharmaceutical Regulatory Affairs & Quality Operations program is structured to provide a comprehensive education over a duration of 2 semesters (1 year). The program is delivered online, offering flexibility for students. Key features of the program structure include:

• Two semesters of study, with a focus on both foundational and advanced topics in regulatory affairs and quality operations.
• Optional work term(s) available, providing hands-on experience in the industry.
• Part-time study options for those who may need a more flexible schedule.
• Courses may be delivered in a flexible format, allowing for both in-person and online participation.

This program meets the Post-Graduation Work Permit (PGWP) eligibility requirements, making it a great choice for international students looking to gain work experience in Canada.

Featured Experiences

The Pharmaceutical Regulatory Affairs & Quality Operations program offers several unique features that enhance the learning experience:

• Optional work term(s) that provide valuable hands-on experience in the field.
• Interactive learning spaces for courses delivered in a flexible format, allowing for both in-person and online participation.
• In-class career workshops and one-on-one coaching to prepare students for the work term.
• Exposure to Canadian and international drug and healthcare legislation, regulations, and guidelines.
• Development of skills in preparing submissions to regulatory bodies and understanding good manufacturing processes.

Career Options

Graduates of the Pharmaceutical Regulatory Affairs & Quality Operations program can explore a variety of career options in Canada, including:

• Regulatory Affairs Associate: Responsible for ensuring that products meet all regulations and standards before they reach the market.
• Regulatory Affairs Assistant: Supports regulatory affairs teams in preparing documentation and submissions to regulatory agencies.
• Quality Assurance Associate: Ensures that products are manufactured according to quality standards and regulations.
• Quality Assurance Investigator: Conducts investigations into quality issues and ensures compliance with regulatory requirements.
• Documentation Administrator: Manages and maintains documentation related to regulatory compliance and quality assurance.
• Medical Information Associate: Provides information and support regarding medical products and regulatory requirements to healthcare professionals.

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