Transitioning from the research phase to the clinical trial phase is a big step for any company, but it also means challenges, not the least of which means your electronic records need to comply with FDA 21 CFR Part 11 and GxP. This can lead to countless hours finding all of the files, compiling them, and ultimately ensuring their integrity from start to finish. The costs of non-compliance can be high, however Egnyte can help.
In this democast, we will review how to deploy and use a GxP-compliant repository using Egnyte’s industry-focused platform, Egnyte for Life Sciences, without sacrificing usability or security, and without creating administrative overhead.
In this demo, you’ll learn how to:
- Easily access your regulated content from anywhere
- Restrict access to only those that need it
- Use tools that make GxP validation fast and easy