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Afra Pharma consultant offer to conduct, manage and monitor multicentre Clinical Trials in a wide range of therapeutic areas and monitor BE studies in India. We have a special interest in Independent Clinical Trial Monitoring Work in India and abroad for sponsors from India and abroad.

  • Medical writing
  • Bioavailability and Bioequivalence
  • Clinical trial studies
  • Analytical solutions

Reports on:

  • Bioavailability and Bioequivalence studies
  • Clinical trial studies
  • Prepare Periodic Safety update report (PSUR)
  • Preclinical studies like toxicity, carcinogenicity, Teratology and Reproduction toxicit