Services
Professional expertise in every detail
The C-TASC statistical consulting group includes Ph.D., M.D./Ph.D. and M.S. biostatisticians who bring decades of hands-on experience supporting the full spectrum of clinical trials. Our professional statisticians possess thorough expertise in multiple statistical software platforms including:
- SAS
- S Plus-t-
- Power and Precision
- NonMem
In addition, C-TASC maintains a team of certified SAS programmers to assist clients in delivering data summaries, graphics and statistical analyses across a wide range of clinical study types.
An integrated approach to delivering data integrity
In order to compile the most comprehensive, thoughtful and well-organized interpretation of data, C-TASC statisticians collaborate with team members throughout our organization to take full advantage of the intellectual assets we can bring to any client project. Some of the typical statistical consulting services C-TASC provides include:
- Sample size determination for micro-array analysis
- Survival Analysis
- Protocol writing
- Longitudinal data analysis
- Sequential monitoring plans
- FDA submissions and proposals
- Manuscript production for publication
- Detailed QC analysis using SAS
We support any or every phase of your process with proven expertise and complex functionality to help you achieve the accuracy, efficiency and scientific integrity you demand.
