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      DMF overseas registration of pharmaceuticals DMF domestic registration of pharmaceuticals GMP compliance audit
      Position:Home > Regulatory services > DMF overseas registration of pharmaceuticals

      Dragonpharm regulatory service introduction


      DMF overseas registration of pharmaceuticals

      Our regulatory services team has a wealth of experience in overseas registration and has successfully assisted many pharmaceutical companies in China in registering EU EDMF files, applying for EU CEP, registration with Japan's JMF, registration with Russia's CIS, registration with other countries in Asia, and registration with South America (Brazil , Argentina, Intellect, Colombia, Mexico), Indian Registration, Middle East Registration (Egypt, Iran, Iraq, Jordan, Algeria) etc.

      With the implementation of eCTD, we can also help pharmaceutical companies edit and submit eCTD.





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