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Regulatory Affairs Uses

 Regulatory Affairs (RA), also known as government affairs, specializes in regulated industries such as pharmaceuticals, medical equipment, agrochemicals (plant safety products and fertilizers), oil, banking , telecommunications, etc. Regulatory affairs often has a very broad definition within the healthcare industries (pharmaceuticals, medical devices, biologics and functional foods).Regulatory affairs professionals (aka regulatory professionals) typically have responsibility for Ensuring that their businesses comply with all of the regulations and laws relating to their company. Working with federal , state and local regulatory agencies and staff on specific issues affecting their business, i.e. working with agencies such as the Food and Drug Administration or the European Medicines Agency (Pharmaceuticals and Medical Devices); the Energy Department; or the Securities and Exchange Commission (Banking). i.e. defining the "regulatory atmosphere" surrounding topics such as the marketing of prescription medications and the enforcement with Sarbanes-Oxley. Regulatory practitioners come from a number of backgrounds. Most regulatory professionals have earned a bachelor's degree, and more than half have advanced degrees, most often in the scientific or technical field. In addition, regulatory practitioners typically have experience in other fields before switching to regulatory affairs.  

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