Manufacturing(OEM & PREMIX)
  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
>> More
Human Nutrition Product
>> More
Active Pharmaceutical Ingredient
>> More
Formulation Product
>> More
 
 
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