The regulatory affairs in healthcare industries is comparatively new & very vital profession constituted by different government regulatory bodies to protect public health, by enhancing or controlling the safety and efficacy of healthcare products that are available worldwide. The one who is dealing with this profession is called as Regulatory Persons or Professionals that are employed in industry, government and academic and are involved with a wide range of products, including pharmaceuticals, veterinary medicines, medical devices, diagnostic services, biologics & biotechnology, pesticides, agrochemicals, cosmetics, & nutritional products. Quality with safety is the major concern throughout this Profession. Most companies, whether they are major multinational pharmaceutical corporations or small, innovative biotechnology companies, have specialist departments of Regulatory Affairs professionals. The regulatory professional''s roles and responsibilities often begin in the research and development phases, moving into clinical trials and extending through premarket approvals, manufacturing, labelling and advertising and post market surveillance.
Loading....