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Regulatory AffairsWith registration experience in US/EU and China, FMD can provide regulatory strategy consultation services as well as document preparation and submission for IND and NDA. Our dedicated RA team possess hands-on experience and solid tracking record in chemical compounds, biological products and medical devices. In addition, intrinsic knowledge of the changing regulatory environment in China and close relationships with regulatory agencies and government labs are our competitive advantage. |
Fountain Medical and ProteLight Receive ChinaBio®s "Most Promising" Award