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Articles In Regulatory Affairs

The regulatory affairs in pharmaceuticals is to assess and perform quality checks to ensures that the veterinary drugs, nutritional supplements and medicinal drugs are rolled out by the pharmaceutical are safe and effective for the people to consume it, in another word regulatory affairs are in place to protect public health. Regulatory affairs in the pharmaceutical consist of variety of functions such as  staying abreast of the change in the legislation of pharmaceutical drug research, manufacture and marketing. Regulatory affairs is a as government affairs, and is an work within in time industries such as medical devices, agrochemicals energy, banking, telecom, pharmaceuticals etc., So the main aim of the regulatory affairs specialist focus on ensuring organization are  meeting all the applicable regulations. The importance of regulatory affairs is to ensure that their companies obey with all of the regulations and laws related to their business. And to ensure that working with federal, state and local regulatory agencies and personnel on specific issue affecting their business. An executive agency of the department of health is MHRA. The MHRA is the Medicines and Healthcare products Regulatory Agency is the government agency responsible for ensuring proper use of medicine and medical devices.

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Citations : 30

Journal of Food and Drug Research received 30 citations as per Google Scholar report

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