Pharmaceutical Regulatory Affairs

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The Pharmaceutical Regulatory Affairs diploma is a program that provides a practical understanding of the regulatory approval and communication processes involving pharmaceutical and biotechnology drugs as well as natural health products and medical devices.

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Toronto Institute of Pharmaceutical Technology

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Program Duration

40 Weeks

Program Intakes
Class Type



OSAP, Grants, Second Career

While the primary emphasis is on regulatory affairs as it applies in North America under the Canadian Health Products and Food Branch (HPFB) and the US Food and Drugs Administration (FDA), our students also learn the regulations in other major jurisdictions such as Europe, Japan and Australia. You will acquire knowledge of international health care system, health care legislation, procedures and practices for regulating the development, manufacture, quality assurance and marketing of health care products.
In just under one year, you can gain the specialized knowledge and practical skills for a lucrative and rewarding career helping to bring new pharmaceutical, biotechnology, natural health, and medical device products to both domestic and international markets. Graduates develop the expertise to work in this challenging area in a variety of roles across the pharmaceutical, biotechnology, medical device, food, cosmetics, natural product, nutraceutical, and other life-science industries.
Program Highlights
eCTD workshops on real drug submissions
Industry relevant training
Training in Health Canada submissions
Small classes optimizing interaction
High employment placement
High entry level salary

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