Analytical  
Environmental Assessments  
Clinical Research  
Clinical Reference Lab Services  
Pre Clinical Safety Evaluations
 
   
 
 

Raw Materials Testing

Drug raw materials are tested as per latest Pharmacopoeial (USP, BP, EP, IP).

Routine analysis includes:

General Identification Tests

  • Complete Compendial Analysis (USP, EP, BP, IP)
  • GC, HPLC and FTIR analysis
  • Pharmaceutical Grade Water testing as per USP and BP
  • UV-Vis spectroscopy
  • Elemental analysis (AA, GFAA, ICP-AES, ICP-MS)
  • Organic Volatile Impurities and Residual Solvents as per USP
  • Heavy metals
  • Elemental (C,H,N,S,O) analysis

In case of non-Pharmacopoeial raw materials development and validation of test procedures are undertaken as per requirement.

   
 
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