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Our comprehensive services covered from protocol development to final study reports,
and are in compliance with ICH-GCP, ISO/IEC 17025 and GLP requirements.

• Protocol Development
• Regulatory Approval
• Ethics Committee Approval
• Study Population
• Clinical Study
• Analytical Method Development & Validation
• Bioanalysis
• Data Management & Statistics
• Report writing & Submission
• Quality Assurance

 
     
     
   
     
 

Our modern in-house 30 beds are available for early clinical trials, bioavailability and bioequivalence studies with special care and treatment from our well-trained medical professionals. We serve our clients with state-of-the-art clinical research facilities with adequate recreation, dining and entertaining functions for volunteers.

    • Total 30 beds (male and female separartion)
    • One ICU
    • Pharmacy to store study drugs (Access controlled)
    • Screening room
    • Sample preparation room
    • Changing room
    • Life saving equipments and drugs
    • Synchoronized clocks all over the company
    • Modern facility with dining and entertaining functions
      • Computers with internet access
      • TV + DVD
      • Book, Magazines, Puzzles, Card games etc.

 
     
     
     
     
   
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