Regulatory Affairs

Regulatory affairs are a field that monitors how foods, pharmaceuticals, and medical devices are produced, tested, manufactured, marketed, and distributed to ensure that they meet regulatory requirements for human consumption. At each stage of product development, regulatory affairs experts are responsible for assuring manufacturers' compliance with applicable global legislative and regulatory standards. The regulatory function in the healthcare industry is critical in ensuring the availability of safe and effective healthcare products around the world. Regulatory professionals include individuals who ensure regulatory compliance and prepare submissions, as well as those whose primary job function is clinical affairs or quality assurance. Regulatory affairs specialists play a critical part in the worldwide population's well-being by overseeing the creation and distribution of safe, healthy goods as well as medical technological breakthroughs.

• FDA
• Clinical trials
• Food industry
• Pharmaceutical industry
• Medical devices
• In vitro diagnostics
• Biologics and biotechnology