Statistical Solutions and SAS Programming
Our skilled persons have kept pace with the Pharmaceutical Industry for over 10 years. We have been involved in the design, implementation and analysis of clinical trials.
At Sheer Consultancy we enjoy working with you, the scientific experts, to discuss the statistical analyses required to achieve your research goals.
We have experienced biostatisticians who have been involved in the preparation of Statistical Analysis Plans in most therapeutic areas and all phases of clinical research.
We offer following services for all type of clinical trials and bioequivalence studies
Statistical Services
- Pre-Clinical and Clinical Trial Consultation
- Sample Size and Power Calculations
- Inputs to Protocol Design and Development
- Randomization Generation
- CRF Review and Annotation
- Statistical Analysis Plan Development
- Phase I-IV and PK/PD analysis
- Interim, pooled or post-hoc analysis
- Meta-analysis
- Statistical Analysis Reports (For Bioequivalence studies and Clinical Trials)
Statistical Programming
- Development of validated SAS Programs
- Writing SAS Macros
- Analysis of primary and secondary efficacy and safety variables
- Creation of derived datasets
- Creation of displays, listings, tables and graphical presentations
- SDTM and ADaM datasets as per CDISC standards
- Preparation of metadata and data Definition (Define.pdf) as per CDISC standards