SimulStat offers off-site biostatistical programming services for situations when you have a project that your infrastructure cannot support. SimulStat has expert knowledge of the FDA Electronic Submission Guidelines and the CDISC data model that is endorsed by the FDA. We have many years of experience in creating individual study reports or integrated reports such as CSS, CSE or 120 Day Safety Updates for both NDA's and BLA's. We can perform any of the following as individual tasks or as a full suite:

• Create individual study or integrated CRTs and analysis data sets
• Create tables, listings and/or graphs for individual or integrated studies or submissions
• Create validation documentation for all programming related tasks

Our team is also experienced in developing data set creation and reporting utilities and macros. Developing and implementing standardized utilities and macros can dramatically increase the efficiency of your organization by allowing your resources to focus on the less mundane and more difficult tasks.

No matter what type of project SimulStat works on, we will:

• Meet your requirements and specifications by being diligent and meticulous.
• Provide accurate, reproducible results by validating the software that we develop.
• Become part of your team by working with your managers, programmers, statisticians and medical writers.