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Regulatory Affairs Importance

 Regulatory affairs is a discipline formed from the need of governments to protect public health by controlling the protection and effectiveness of drugs in areas such as pharmaceuticals, veterinary medicines , Medical devices, pesticides, agrochemicals, cosmetics and complementary medicines and the discovery, research, manufacture and marketing companies responsible for these products. A new generation of practitioners has arisen to deal with these compliance problems for businesses. Most companies, whether major multinational pharmaceutical companies or small, innovative biotechnological companies, have specialized regulatory departments. The success of the regulatory strategy depends less on the regulation than on how it is interpreted, applied and communicated within companies and to outsiders. The task of regulatory affairs is to establish and enforce a regulatory strategy to ensure that the joint efforts of the drug development team result in a product that is appropriate to global regulators but is also in some way distinguished from competition and also to ensure that the activities of the business, from non-clinical research to advertisement and promotion, are carried out.  Regulatory affairs is an attractive career choice for science-based graduate students who enjoy communication and teamwork, are comfortable with multi-tasking, and are eager to expand their knowledge across the wide range of the pharmaceutical world. Regulatory affairs are a lucrative, intellectually challenging and highly regarded career within pharmaceutical companies.  

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