The B.E. Centre had been carrying out Bioequivalence study most satisfactorily since 2002 being approved by DCGI Oct-2002.

ONLY CENTRE IN EASTERN REGION

We offer our expertise in 

  • Bioavailability & Bioequivalence Studies
  • In-vitro dissolution & shelf life studies
  • Accelerated Stability Studies
  • Controlled Release formulations 
  • Toxicity studies
  • Pharmacokinetic & Pharmacodynamic Studies

Apart from rendering satisfactory Services to the Various Pharmaceutical Industries other specialized areas where centre has started exploring its Research Capabilities are :

  • Identification & Characterization of drug metabolites
  • Drug Interaction Studies
  • Clinical Trials
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