White Papers

White Paper Download

Bring repeatability and automation to the data integration process with SAS® Clinical Data Integration

The life sciences industry is under pressure to accelerate time-to-market for new compounds – at lower cost. Traditionally, the process of managing clinical trials data has been cumbersome and resource-intensive. Industry analysts have stated that automated data integration and validation can trim 30 to 50 percent from the clinical trial cycle. This white paper makes a case for implementing data standards and applying automated processes for managing data throughout the clinical trials process, from study design to regulatory submissions. It also describes how SAS Clinical Data Integration provides value for sponsors, CROs and regulatory authorities through mature data transformation capabilities, embedded CDISC capabilities, the ability to automate repeatable processes and the flexibility to support the evolution of both new and custom models.

Have a SAS profile? Log in to pre-fill the form.

*  First Name
*  Last Name
*  E-mail Address
* Organization/Company
* Industry
* Job Title
*  Country
(Required for Canada and U.S.)
* Business Phone
Yes, I would like to opt-in to receive occasional emails from SAS and its affiliates
about SAS events, free white papers, special offers on training and publications, etc.
All personal information will be handled in accordance with the SAS Privacy Statement.

( * indicates required field )