Clinnovo provide comprehensive biostatistics and statistical programming services to support clinical, pre-clinical, epidemiology, health economics and patient reported outcomes for pharmaceutical, medical devices and biological companies.

Clinnovo works with major pharmaceutical companies as a preferred services provider of SAS programming and reporting analysis for Phase I-IV clinical trials. We have a solid team of experienced SAS programmers, many of which are SAS Base and/or advanced certified and have on average 3-5 yrs Pharma/biotech experience programming listings, tables, graphs across all phases.

We provide a complete range of statistical programming expertise, including the following:

• Trial design
• Sample size and power calculations
• Descriptive statistics
• Statistical protocol development
• Statistical programming
• Creation of derived datasets

Creation of displays, listings and graphical presentations

• Application of sampling weights
• Determination of standard errors
• Significance testing
• Multivariate analysis
• Nonlinear regression
• Survival analysis
• Proportional hazard analysis
• Statistical matching
• Statistical imputation
• Statistical automation
• Statistical analysis plan writing
• Statistical and clinical report writing
• Statistical support to Data and Safety Monitoring Boards (DSMBs)
• Pooled analyses for summaries of clinical safety (SCS; formerly ISS) and efficacy (SCE; formerly ISE)
• Conversion of legacy data to the ADaM and SDTM standards
• Data mining