Fast, accurate, and informed data analyses
Our statistical programming staff averages over 15 years of experience in the industry and more than 8 years at Rho. Our statistical programmers are engaged throughout the entirety of a clinical development program. We bring this experience and engagement to your product and, as a result, provide fast, accurate, and informed data analyses that you can rely on.
Rho’s highly experienced statistical programming group has implemented data standards; performed quality control; and executed pharmacokinetic, dose ranging, dose finding, safety, and efficacy analyses on over 200 protocols across a wide range of therapeutic areas over the last two decades.
Rho’s statistical programmers are an integral part of the clinical study team and central to producing accurate, interpretable results that allow you to evaluate the safety and effectiveness of your product. Our statistical programming group integrates with the study team to fully understand study conduct, data collection questions, potential data anomalies, and analysis-related decisions.
Among Rho’s many statistical programmers are numerous industry experts and leaders in data standards as well as clinical data programming technologies and software. Our experts are frequent presenters at CDISC, SAS, PhUSE, DIA and other industry conferences. We apply this experience to your clinical development program to streamline the clinical data quality control and data analysis process.
Our statistical programming group provides the following services:
- eTMF-ready documentation
- SDTM clinical database development
- ADaM analysis database development
- Integrated ADaM analysis database development
- Tables, Listings, and Figures quality control and production
- Interim analyses, blinded analyses, and unblinded analyses for all stages of protocol analysis
- Ad hoc and exploratory analysis
- Poster and publication analysis support