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WEBINAR

WEBINAR : Bridging the Gap between GxP Validation and Assurance
FEATURING: Egnyte for Life Sciences & xLM
DURATION: 30 minutes

Bridging the Gap between GxP Validation and Assurance


Today, companies use a variety of cloud software to manage regulated data produced in GxP environments (e.g, clinical trials, manufacturing, etc.). Maintaining compliance and validation is a challenge with continuously-updating Software-as-a-Service.

In this webinar, we will demonstrate continuous validation software from xLM, an Egnyte partner. Their product enables customers to stay compliant with new releases and reduce documentation, all the while providing users with access to the latest features.

Using Egnyte’s industry-specific platform, Egnyte for Life Sciences, as an example, our team will also show you how our specialized GxP software natively helps companies store and manage documentation and comply with FDA 21 CFR Part 11 or Annex 11. During the webinar, you will learn how to:

  • Exchange and manage data with external collaborators

  • Control validation timelines and costs

  • Keep regulated data in the cloud

  • Facilitate continuous validation

Interested in learning more about xLM? Check out their website here.


Nagesh Nama
Chief Quality Officer
xLM
Tim Johnson
Director of Product Marketing, Life Sciences
Egnyte

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