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Tag: regulatory affairs training

What Students in Regulatory Affairs Training Should Know About the USMCA’s Biologic Protections

The United-States-Mexico-Canada Agreement, or the USMCA, is a free trade agreement between the three neighbouring countries, to replace the North American Free Trade Agreement (NAFTA), which was in place for 25 years. The USMCA introduces new regulations on biologics, affecting data protection and the price of medicine, as well as expanding on the definition of […]

How to Achieve Supreme Attention to Detail during Regulatory Affairs Training

Accuracy and attention to detail in the pharmaceutical industry is beneficial not only for employees and organizations, but for the general public who are receiving medications after they have been released to the marketplace. During the development process, professionals working in regulatory affairs are required to exercise a great deal of precision and accuracy in […]

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 […]

Evolving Perceptions of the Pharmaceutical Industry: How Regulatory Affairs Diploma Holders Can Play a Role

The development and production of new medicines to help those in need makes pharmaceutical careers very rewarding. New drugs and products are constantly being discovered and lead to breakthroughs in treatment and prevention that make the world a better place. However, while the industry remains a necessity in the modern world, consumer trust has become […]