GxP-Compliant Data Repositories for SAS JMP Analysis

Modern clinical trials produce large volumes of regulated data across numerous clinical sites. Data science teams often use tools, like SAS, JMP, or R, to glean insights from this data. However, whether in the cloud or on-premise, accessing these files for analysis, while complying with FDA 21 CFR Part 11, is a challenge.

In this demo, we will show you how our industry-specific platform, Egnyte for Life Sciences, can help you collaborate on clinical data sets and analyze them easily in statistical tools, namely SAS JMP. Our unique combination of cloud and on-premise software facilitates a seamless data analysis workflow, while maintaining GCP/GxP compliance.

Egnyte’s Life Sciences Director of Product Management, Harith Kesari, and Director of Products, Hari Krishnan, walk through the architecture of the solution and how to maintain chain of custody. With an increasingly remote workforce, collaboration is more important than ever.

In this session, you’ll learn how to:

• Analyze clinical data from Egnyte in SAS JMP
• Maintain Part 11 or GCP compliance for raw & analyzed regulated data
• Gain best practices for managing large files remotely