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    Regulatory Affairs
    Regulatory Affairs
     
    Registration of our products in USA, Europe, Australia, South America and Russia
    Documents compilation & supplement, make facility GMP compliance
    Updated registration rules studying and training
    Key paper work mainly include
    Impurities Profiling
    Analytical Method Development
    Process validation guideline
    Stability Study Management
     
     
    Products
     
    Animal Health Product
    Human Nutrition Product
    Active Pharmaceutical Ingredient
    Formulation Product
     
     
     
    Contact us | E-mail:vega@vegapharma.com
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    Tel:86-571-88398112