From Pre-Clinical Analysis to Submission SAS® Can Help You Along the Path
Wherever you are in your clinical trials, SAS can help you do it more efficiently and effectively. In this infographic, you'll get a look at the ways in which SAS can help you securely manage, scale and maintain your data - whatever your programming language, data sources or analytics techniques.
How can SAS assist with clinical trials?
SAS can help teams manage and analyze large volumes of complex data efficiently, which is crucial for increasing the speed of bringing products to market. Whether you're in pre-clinical analysis or early phases of clinical trials, SAS provides tools that allow for powerful statistical analysis, flexible programming, and a centralized data repository to streamline the process.
What features does SAS offer for regulatory submissions?
The SAS platform is designed to be submission-ready, offering GxP compliance and 21 CFR Part 11 enablement. It allows for auditable actions, traceability of data, and repeatability of analysis, which are essential for meeting regulatory requirements. Additionally, it supports both SAS and R programming, making it adaptable for various user needs.
Who can benefit from SAS in the Life Sciences sector?
SAS serves a wide range of companies in the Life Sciences sector, from small and medium-sized enterprises to large organizations, including many in the Fortune 500. The platform is scalable, accommodating anywhere from a handful of users to over 1,500, making it suitable for diverse operational needs across biotech, pharmaceuticals, biologics, and medical devices.
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