CR Toolkit™ SAS Macro Library
Partner with us to organize your data efficiently
Clinical trial management involves substantial quantities of code which may be difficult to navigate, and subsequently might hinder your ability to go to market with your product effectively. At Navitas Data Sciences, we understand the importance of clinical trials data in FDA approvals, and in the need for life-saving drugs. We help you organize, and structure accurate clinical data which will enable your life-saving products to get regulatory approval and reach patients faster. Our CR Toolkit™ enables you to work efficiently with study reports, helping you access your data accurately and consistently.
Gain with our CR Toolkit™
SAS Macro Library
Standard Call Interface
Fully Documented Validation Package & User Manual
CR Toolkit™ transforms your data
Your clinical trial data needs to be transformed into easily understandable drug information, following the strictures of approval and regulatory bodies. This data transformation is a critical step that will pave the way for a faster market availability of your product. As you conduct multiple studies and file for regulatory approvals, there may be changes to your protocol, personnel and reporting requirements. Such changes affect your data, and in turn, the information for your regulatory submissions.
Our CR Toolkit™ enables you to transform data quickly and effectively, enabling you to be compliant and provide a high-quality output. The CR Toolkit™ SAS macro library facilitates preparation of reports conforming to the highest standards. It enables you to assemble and produce consistent reports time after time. You can work with any data structure and content, and it supports CDISC standards (ADaM and SDTM).
CR Toolkit™ Key Benefits
Reduces lines of code & development time by over 50%
Reduces variability by standardizing statistical operations
Enables consistency throughout your programming environment
Streamlines QC process
Why choose a CR Toolkit™?
CR Toolkit™ is an innovative system that will help in streamlining the numerous codes in a clinical trial and help in effective reporting of data. With CR Toolkit™ you can design tables quickly and consistently, every time. CR Toolkit™ is 21CFR Part 11 compliant and has been used in numerous clinical studies. It helps in improving productivity, quality and aids in lowering costs and time.