• Design & development of clinical trial databases & registries
• Development of e-CRFs
• Development of data management & statistical analysis plans
• Data entry & validation
• Study design-dependent sample size calculation
• Statistical analysis of data derived from clinical trials
  • Observational studies, equivalence trials, superiority trials, non-inferiority trials, bioequivalence studies
• Preparation of full & abbreviated reports
• Medical scientific writing
  • Abstracts, Posters, Presentations & Manuscripts for publication purposes
• Meta-analysis
• Analysis of genetic & pharmacogenetic studies