oneQMS
CAPAManage corrective and preventive actions
Change RequestReview and control quality changes
DeviationTrack and resolve process deviations
IncidentRecord and investigate quality incidents
Audit ManagementPlan and manage audit activities
Vendor ManagementMonitor supplier quality and compliance
Customer ComplaintCapture and resolve customer concerns
Quality IssuesCentralize and resolve quality issues
OOS/OOTInvestigate out-of-specification results
eLogsMaintain secure electronic records
Also in Products
Document Management
Training Management
Services
Company
Resources
OneQMS Module
Why Astakenis
Content for Why Astakenis page from the OneQMS website content document.
Overview
Replace this section with the approved content for Why Astakenis. This template uses the shared OneQMS design system.
Key Features
- Configurable workflows
- Electronic approvals
- Complete traceability
- Audit-ready records
Key Capabilities
Workflow Automation
Automated assignments and approvals.
Compliance
Built for GMP, GxP and FDA requirements.
Audit Trail
Complete visibility and accountability.