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