¡ô MINISTRY OF HEALTH PEOPLE REPUBLIC OF CHINA
¡ô BEIJING DRUG ADMINISTRATION
¡ô CMDI
¡ô CMD
¡ô CCC
¡ô
STATE FOOD AND DRUG ADMINISTATION (SFDA)
¡ó
The document requirement for the Certificate retri...
(2008-2-18)
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Provision on the Registration and Inspection of In...
(2008-2-18)
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Provisions on the Classification of Medical Device...
(2007-12-10)
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Beijing Pharmaceutical Company Ltd. Medical Appara...
(2007-12-10)
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Federal Communications Commission (FCC) Seeking In...
(2007-12-10)
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Regulations for the S&A of Medical Devices...
(2007-12-10)
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Supervision & Administration on...
(2007-9-25)
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Medical Device Manufacturing Enterprise...
(2007-9-25)
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State Drug Administration Order...
(2007-9-25)
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Provision on the Registration and Inspection of......
(2007-9-25)
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SFDA issues Guideline...
(2007-9-21)
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Standard Registration Procedure...
(2007-9-21)
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Re-registration of import products...
(2007-9-21)
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Initial registration of import products...
(2007-9-21)
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SFDA issues six working procedures including Proce...
(2007-9-21)
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SFDA issues the No.89 announcement of drug adminis...
(2006-8-4)
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Change requirement in SFDA Registration Certificat...
(2005-12-30)
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How To Get A Drug License In China...
(2005-12-26)
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