Audience
Medical device businesses searching for an electronic quality management system solution
About Virje
Virje complies with the requirements of 21 CFR Part 11, 21 CFR Part 820, and ISO 13485. Overwhelmed by the thought of Part 11 software validation? Accessible from wherever you are, for whenever you work. Eliminate paper, reduce cost, and increase efficiency with automation and centralized collaboration. Perfect for small to medium-sized businesses. Built from the ground up specifically for medical device quality management. A system that is flexible enough to adjust to your workflows and processes, without having to compromise. Configurable change order approvals by employee role and by document type. Notifications to responsible personnel at every stage in the change process. Ability to designate material dispositions for individual documents. Easy access to released and historical versions of documents. Quick viewing of document change history. Tracking of where-used locations and distributed hard copies. Periodic document review notification.
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Integrations
No integrations listed.
Company Information
Virje
United States
www.virje.com
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Product Details
Platforms Supported
Cloud
Training
Documentation
Support
Online
Virje Product Features
Quality Management
Complaint Management
Corrective and Preventive Actions (CAPA)
Document Control
Equipment Management
Audit Management
Compliance Management
Defect Tracking
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management