Unifying quality processes, content, and training management onto a single cloud platform drives GxP compliance and operational excellence. Egnyte reduces the administrative burden of running an effective quality process by streamlining review and approval workflows, automating document status and providing comprehensive reporting capabilities.
Control GxP documents with automated review and approval workflows.
Achieve greater visibility and control over regulated content and data across all GxPs.
Increase training efficiency and compliance with an end-to-end solution.
Streamline Quality document management, removing bottlenecks to regulated business processes.
Accelerate the review and approval process with real-time cloud-based collaboration tools, notifications, and native Part 11-compliant e-signatures.
Easily define version numbers for new documents, set expiry dates and ensure only effective copies are available.
Integrate with existing IT infrastructure and quickly implement and validate the solution for rapid time to value.
We needed a solution that would augment our workflows to keep the drug development on track, regardless of the location of each team. I had come across Egnyte a couple of times and with a little more investigation saw greater potential than performance alone.
See How Egnyte for Life Sciences Streamlines
Quality Document Management