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rajesh@azicopharma.com
 
 
 
 
 

Azico undertake Custom / Contract synthesis on exclusive basis for APIs & Intermediates for Innovator & Generic companies. Also take custom synthesis of complex molecules.

To support its activities Azico has :

  • State of art Kilo Level cum Pilot Plant complying to cGMP requirement with its dedicated clean room areas up to packaging of final products
  • Plant is suitable for Audits by USFDA/EMEA/PMDA and any regulatory agencies
  • R&D laboratory is fully equipped for Milligram to kilogram level scale up of APIs and APIs intermediates.
  • R&D facility is equipped with international standard fume hoods and walk-in types fume hoods, hydrogenators and other equipments to perform all types chemical reactions.
  • Azico has state of art analytical equipments :
  • HPLC with LCMS
  • HPLC PDA Detector
  • HPLC Preparative for impurity isolation
  • HPLC for routine analysis
  • GC Head Space
  • GC Regular
  • Azico with cGMP Plant and Quality Systems of ICHQ7 is capable for assisting customers for :

    Identification of Routes Safety Data Management,
    Product Development, Continual Process Improvement
    Synthesis & Scale-Up from milligram to kilo to ton level,  Impurity Synthesis
    Analytical Method Development IPR Protection Support
    Validation  

     

     
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