Though the requirements for review of drug registration in China are more and more in accordance with ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use), there are still lots of differences and special local requirements. we know how to guide the manufacturer on preparation of CFDA Application Dossier, and avoidance of failures and defects in registration procedure, Help foreign manufacturer obtained IDL (Import Drug Licence) successfully! We are engaged in the fields of pharma, medical device, health food,cosmetics products CFDA & MOH registration business almost 10 years, help the dozens of manufacturers, hundreds of products to enter Chinese market.
is eligible to be your LA in China with the help of our office in Beijing, Shanghai & Guangdong. Appointed CFDA LA must be a legal entity and maintain a place of business in China.
The CFDA requires that all Pharmaceutical companies which located out of China must appoint a registered Legal Agent (LA, in-country regulatory representative).
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