GxP compliance made easy! Learn how to streamline the management of quality documents using innovative collaboration and automation features.

Egnyte helps life sciences companies maintain compliance by streamlining the management of quality documents using innovative collaboration and automation features.

• You can schedule the promotion or retirement of effective documents to ensure the latest information is available to end users.
• Co-editing enables real-time collaboration, removing bottlenecks and accelerating the review and approval process.
• The Quality App keeps track of the status of future effective, effective, and obsolete documents in one central location.

Manage the complete lifecycle of regulated documents and automate the deployment of effective documentation, all on a unified, easy-to-use, GxP-compliant platform.