Regulatory Support

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The role of mediSMART regarding regulatory support in clinical researches is to provide guidance to pharmaceutical companies in compliance with applicable local regulations and guidelines which enable them to conduct clinical researches in most feasible ways. The successful execution of our activities depend on perfect collaboration with our clients and regular internal training programs. Our regulatory support principles are performing quality checks on submission documents to ensure that all necessary documents are completed and in place, continuously reviewing guidelines and regulations to develop timely solutions for possible issues and facilitating medical device study submissions and marketing applications by providing regulatory insight.