Egnyte for Life Sciences Quality equips Quality teams with compliant tools to manage regulated documents efficiently under GxP and FDA 21 CFR Part 11 standards. The platform supports native workflows for document review, approval with Part 11-compliant e-signatures, and real-time collaboration. It ensures only effective versions are accessible, tracks document adoption and status, and simplifies permission assignment with configurable roles. Built for rapid deployment and ease of use, Egnyte offers audit-ready features like detailed audit trails, data integrity checks, and granular access controls—enabling scalable, streamlined, and compliant quality processes across the organization.

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