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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 and abroad. We have a special interest in Independent Clinical Trial Monitoring Work in India and abroad for sponsors from India and abroad.

  • Medical Writing & Clinical Studies
  • Bioavailability
  • Bioequivalence
  • Clinical Trial Studies
  • Analytical Solutions

Reports on

  • Bio availability / Bio equivalence Studies
  • Clinical Trials studies
  • Prepare Periodic Safety Update report (PSUR)
  • Preclinical studies like Toxicity, Carcinogenicity, and Teratology & Reproduction toxicity


We are in association with ISO certified, ICHGCP compliant Clinical Research & Consulting firm which is dedicated to provide clinical study related services for pharmaceutical and biotechnology product development sculpted to offer high quality design, conduct and analysis of a clinical trial which constantly try to innovate in order to provide easy solutions to our clients for their prestigious projects. To accomplish this, we strive to provide our clients with exceptional services under one roof for the vast sector of Clinical Trial management and Bioinformatics developments.

In Clinical Research, our services range from Site Services to Sponsor related, regulation of Monitoring issues, management of the Clinical Trial data, precise Scientific Writing and the developing Post Marketing Strategies; strictly adhering to the respected regulatory compliance summed up with our personal commitment to time management and unbiased report submissions.