DMF overseas registration of pharmaceuticals
DMF domestic registration of pharmaceuticals
GMP compliance audit
REGULATORY SERVICES
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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.
