Life Sciences Analytics Software

Life sciences analytics for capitalizing on big data to foster 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. SAS delivers:

• 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.

Learn about SAS^® Life Science Analytics Framework

For more than 40 years, SAS has provided clinical trial data management and analysis solutions. We monitor life sciences research trends so we can provide innovative solutions that solve tomorrow's challenges. With SAS, you can promote fast, efficient information sharing, improve the validity and safety of clinical trials, and get better products to market faster. SAS also helps you:

• Provide secure, global access to a centralized clinical knowledge base of consolidated, clean and standardized data from diverse sources.
• Gain clinical insights quickly using core statistical analysis, data preparation, data visualization and advanced analytics – such as data and text mining, forecasting and optimization.
• Easily and seamlessly implement industry standards such as those provided by CDISC, since rel­evant standards support is built into our core software.

Learn about SAS^® Life Sciences Analytics Framework

Controlled access to patient-level data for valid research purposes. The ability to analyze data from the clinical trials on which regulatory decisions are based. Our clinical trial data transparency solution delivers:

• Secure data access. Grant authorized researchers access to de-identified patient-level clinical trials data through a secure clinical trials data repository.
• Analytics for research. Enable researchers to analyze data using industry-leading analytics.
• Flexible implementation options. Have the flexibility to support a company’s data transparency initiative or to provide shared access to clinical trials data from multiple companies.

Establish a secure clinical trials data repository. Give authorized researchers access to the data and powerful analytics. And rely on a company that life sciences organizations have trusted for more than three decades. As the market leader in clinical trials data transparency initiatives, SAS enables you to:

• Give researchers access to the data they need. A secure clinical trials data repository ensures that authorized researchers have access to specified clinical trials data for their research purposes.
• Empower researchers with embedded analytics. Because industry-leading analytic technologies are embedded into the system, researchers can derive greater insight from clinical trials data.
• Take advantage of more than three decades of industry experience. SAS is globally recognized as the industry leader in business analytics and the de facto standard for clinical trial data analysis and reporting in life sciences. And we bring all that expertise to you.

Real-world data from all relevant sources. A vast array of analytic tools for real-world evidence projects. And faster time to the insights you need for pipeline and commercialization decisions. SAS delivers:

• Proven, powerful data management. Easily integrate real-world data from both internal and third-party sources – e.g., clinical, claims and consumer health care data.
  
• Fast access to real-world evidence. Even nontechnical users can navigate, visualize and explore huge amounts of data quickly with an easy-to-use, point-and-click interface to powerful, in-memory analytics.
• A complete analytical toolset. Choose from a wide range of analytic tools – from easy-to-use data visualization, to statistical programming, to more advanced data mining techniques – infused with cutting-edge, innovative algorithms that can help you extract evidence from real-world data sources to solve even your most complex problems.
  

Better assess the benefits, risks and cost-effectiveness of treatments based on actual patient outcomes and the total cost of care. Develop better therapies to improve patient care, provide evidence for payers and differentiate your brand in the health care market. And help ensure the best health outcomes and economic value for targeted patient populations. With SAS, you can:

• Easily integrate real-world data from multiple sources and vendors. Spend less time preparing data and more time extracting valuable, real-world insights. Our leading data management capabilities ease the time-consuming process of gathering and preparing real-world data for analysis.
  
• Go far beyond traditional query and reporting. Visually explore complex data sets of any size quickly and efficiently. Gain insights into key issues like brand strategy, treatment regiments, pricing, reimbursement and formulary access. And create meaningful reports that you can share via mobile devices.
  
• Build an analytical foundation for real-world evidence. Give programmers, analysts, researchers and statisticians a comprehensive analytical toolset for building programs and models that can extract evidence from real-world data sources for pipeline and commercialization decisions.