According to the order of drug research and development and marketing

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According to the order of drug research and development and marketing

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According to the order The first original research new drug to be market is call an “original drug”. After the patent of this product expires or the patent is authoriz, the products produc by other manufacturers in accordance with the relevant standards of this “original drug” are call “generic drugs”. In fact, the common concept internationally is call “generic drugs”, which specifically refers to generic drugs develop and produc by other mauritius email list 150000 contact leads pharmaceutical companies after the patent of original new drugs or patent drugs or brandname drugs expires, with the same active ingrients, dosage forms, routes of administration and therapeutic effects, which can be replac with each other in clinical treatment.

Vigorously developing “generic drugs”

Is of great significance for rucing drug costs, alleviating the burden on patients, and enhancing the accessibility of drugs, and is also a common competitive analysis: what is it and how to perform it practice in the world. All countries have made the generic drug industry a priority for support and development. For example, 90% of prescriptions in the U.S. pharmaceutical market are for generic drugs, also known as generic drugs. Many wellknown large multinational pharmaceutical companies also regard the research and development and production of generic drugs as an important part of their business.

Generic drugs are also an important part of my country’s pharmaceutical industry

In order to improve the quality of generic drugs, the State Council issu the “Opinions on Reforming the Drug and Mical Device Review and Approval System” in August 2015, which clearly adjust generic drugs from “imitation of drugs with existing national calling list standards” to “imitation of drugs with quality and efficacy consistent with original drugs”, and accelerat the consistency evaluation of generic drugs from 2016. The evaluation standards were also further clarifi. In principle, the bioequivalence test method should be adopt to achieve international standards According to the order.

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