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Tag: pharmaceutical regulatory affairs

How Regulatory Affairs Courses Apply to Health Foods

The specialized skills in a regulatory affairs program equip you to work in various industries, one of which is the food industry, including neutraceuticals. Nutraceuticals are foods that have medicinal benefits and are taken for health purposes. Foods with health benefits aren’t limited to neutraceuticals, however. You’ll find health claims made on various foods through […]

A Guide to Drug-Device Combinations for Students in Pharmaceutical Regulatory Affairs

Because combination products are both pharmaceuticals and medical devices, such as inhalers or pre-filled syringes, they present the tricky task of combining two types of product, while making sure regulation is satisfactory. This means that in your career in pharmaceutical regulation, you may have to work in scenarios where two different approaches need to be […]

Why Generic Drug Approval Changes Matter If You’re Studying Pharmaceutical Regulatory Affairs

Generic drugs play an important role in Canada’s pharmaceutical industry. They also play an essential role in the health and wellbeing of many Canadians, who are able to receive relief and treatment for their medical conditions without paying the higher costs associated with name-brand drugs. Recently, Health Canada has proposed certain amendments to the Food […]

Injections vs Tablet Treatments: The Differences Explained for Students in Regulatory Affairs Courses

Are you seeking a way to advance your existing science skills and gain the practical qualifications to begin a lucrative career in the pharmaceutical sector? Earning your Regulatory Affairs Diploma will place you at the forefront of the industry, providing you with the skills needed to support the licensing and approval of pharmaceutical drugs. To […]

How Pharmaceutical Regulatory Affairs Training Helps to Ensure Medical Device Safety

In addition to working with various types of drugs, cosmetics, medicines, and other pharmaceuticals, medical devices fall into the category of products that require regulation before being approved for organizational and public use. Medical devices can include any number of products used in treatment, alleviation, diagnosis, or disease prevention for certain physical conditions. The most […]