Our Services
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