Description
Global collaboration based on accurate clinical research information. Rapid clinical trial insights that let you accelerate promising programs or stop unproductive ones. And streamlined processes that get your products to market faster. SAS is the de facto standard for clinical trials data analysis and reporting, and electronic submissions to regulatory authorities, such as the FDA. Our life sciences solutions include:
Support for CDISC. Standardize your clinical trials data and validate its adherence.
Risk-based monitoring. Optimize the scheduling of site visits and oversight by analyzing site and study data. Use advanced analytics to identify potential risks early enough to proactively address them.
Statistical analysis and reporting. Access and analyze clinical trials data to support clinical development decisions and submissions.