Скачать или смотреть Xybion QMS DMS Overview | Streamlined Document Management for Regulated Industries

Gain complete control over your regulated documents with the Xybion QMS Document Management System (DMS). In this video, we walk you through the powerful capabilities of our digital DMS, which is engineered to help life sciences and manufacturing organizations maintain compliance, reduce manual errors, and streamline document workflows.

Xybion’s cloud-based DMS enables centralized document creation, review, approval, version control, and archival—all within a secure, 21 CFR Part 11-compliant environment. Whether you’re managing SOPs, training records, specifications, or quality manuals, Xybion QMS provides end-to-end visibility and automation to improve efficiency and reduce compliance risk.

Built specifically for highly regulated industries, Xybion QMS DMS helps you stay audit-ready with automated audit trails, electronic signatures, and secure access controls. The platform supports ISO 9001, FDA, GxP, and global regulatory standards, ensuring your documentation is always inspection ready.

Watch this overview to see how Xybion QMS DMS empowers teams to collaborate in real time, eliminate paper-based processes, and maintain a unified foundation for all quality-related documents.

📁 Smart Document Workflows

🔐 Secure, Compliant Access

📊 Real-Time Collaboration and Tracking

✅ Ready to simplify document control? Book a personalized demo now!
https://www.xybion.com/lp-landing/qms...

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