The SAS Clinical Standards Toolkit shows promise for delivering a robust SAS based framework for managing standard metadata. It includes the ability to manage a global standard (i.e. SDTM) as well as individual studies. The first release provides the capability to run the standard SDTM and Janus checks as well as create the define.xml. d-Wise has spent time assessing the capabilities of the Toolkit and has developed services to help your organization get started with the solution.
d-Wise will provide following services to help your organization gain a better understanding of how to implement the Toolkit.
- Help navigate the challenges of installation and configuration
- Provide an overview of the Toolkit framework
- Review the process of setting up and configuring a clincial study
- How to execute validation checks and create define.xml
- A step by step tutorial on the various macros, configuration files, and validation steps
In additon, d-Wise offers an optional workshop where our consultants will work side by side with you to move your current clinical trial data into the Clinical Standard Toolkit Framework.
Please contact d-Wise at This e-mail address is being protected from spambots. You need JavaScript enabled to view it for more information on the services we can provide to your organization. You can also download the Services brochure located in the Resources section to the left.
SAS Toolkit Services
