Drug regulatory affairs training Drug regulatory affairs masters play a crucial role in ensuring all pharmaceutical products comply with regulations governing the industry. Those working in drug regulatory affairs jobs not only work in the initial application phase for a new or generic drug but also in the licensing and marketing stages – making sure all operations and products meet required safety and efficacy standards. Professionals must combine knowledge of the business, legal and pharmaceutical industries to determine if regulations are being followed and in many cases form the link between pharma companies and regulatory authorities, such as the Food and Drugs Agency (FDA) and the European Union. Regulatory affairs jobs in the India and further afield are generally within the pharmaceutical, chemicals, biotechnology, medical devices, and cosmetics industries. Organizations such as the FDA, also provide roles for those inter...