WorkFlow
CAPAs
Eliminate the cause of existing or potential nonconformities in order to prevent recurrence with a comprehensive CAPA workflow. CAPAs based on smart controls and effective procedures allow your quality management system to integrate changes across workflows – connecting with risk, product, and process changes. With fully integrated training across the CAPA module, your records are complete and audit ready.
CAPAs Feature List
Corrective and preventative action workflows allow identification and analysis of product and quality problems in accordance with the regulation and best practices.
Root Cause Analysis
Fully document and your root cause analysis
Risk Management
Ensure CAPAs are evaluated for impact to product or quality management system risk
Customizable to international jurisdictions
Fully customizable to accommodate all of your internal audit requirements
Risk Impact Assessment
Upload or document your risk impacts with full electronic signoff
Automatic Record Generation
Generate CAPA records quickly and easily
Supports Attachments
Ensure all applicable files are provided and available
Easy download for sharing
Share CAPAs with suppliers or other key partners for easy resolution
Manage Approvals
Fully customized approval workflows