Drug Regulatory Affairs refers to all aspects within the pharmaceutical development process and how they are subject to various degrees of regulation. Regulatory Affairs (RA), also called Government Affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, and banking.Regulatory affairs is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines, and by the companies In pharmaceutical regulatory affairs, candidates with pharmacy degrees ... that are above your level of skills and experience, instead use this time more wisely to Citation Report of the Pharmaceutical Regulatory Affairs: Open Access offers detailed ... A Country Perspective in Exploring the links between Hospital Pharmacies and ... The Use of Medicinal Plants in Human Healthcare: A Scoop on Safety. Regulatory affairs (RA), also called government affairs, is a profession within regulated ... pharmaceuticals; medical devices; in vitro diagnostics; biologics and biotechnology; nutritional ... on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use