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
Animal Health Product
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Human Nutrition Product
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Active Pharmaceutical Ingredient
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Formulation Product
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