Our Services

• Bioequivalence & Bioavailability studies
  • Up to 40 beds,
  • Pool of 70 healthy volunteers,
  • Fully qualified medical and analytical team.
• Pharmacokinetics, pharmacodynamics & statistical evaluation
  • Protocol and study design,
  • Case report form design,
  • Sample size estimation and randomization,
  • Adverse event reporting,
  • Biostatistics,
  • Pharmacokinetics and pharmacodynamics modeling and reporting.
• In-vitro Dissolution Studies:
  • Biowaivers and comparative in-vitro dissolution.
• Bioanalysis:
  • Method development and validation,
  • Drug and metabolite determination in biological fluids.
• Drug stability studies:
  • Accelerated stability studies,
  • Long-term stability studies.
• Bioequivalence and Bioavailability studies
• Pharmacokinetics, pharmacodynamics and statistical evaluation
• In‑vitro dissolution and biowaiver studies
• Bioanalytical method development and validation
• Drug stability studies (accelerated and long‑term)
• Pharmaceutical and herbal analysis
• Formulation development studies
• Microbiological analysis
• Skin sensitivity and eye irritation tests
• Determination of Sun Protection Factor (SPF)
• Determination of total flavonoids and alkaloids
• Water and oil analysis