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 Specialists usually get an average salary of Sixty Five Thousand dollars per annum. Regulatory Affairs Specialists are compensated most highly in the District of Columbia, which has average pay scales of approximating $77520. this department helps safeguard product life cycle and guide the company on regional and global laws/regulations set forth by different regulatory authorities. These rules and regulations are now a part of daily practice of pharmaceutical regulatory affairs professionals working for different industries. Due to this practice, the regulatory professionals think that an improved environment for the health community has emerged, serving the public in a more ethical and better way. Still there is much room for restructuring the health authority Regulatory Affairs (RA), also called Government Affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, and banking. ... Pharmaceutical companies use all the data accumulated during discovery and development stages in order to register the drug and thus market the drug