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- 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