MANUFACTURING QUALITY
Optimize manufacturing and quality performance with fully integrated digital quality processes
TrackWise Digital Manufacturing Quality
2x EFFICIENCY GAINS
Reduced outstanding training records to less than 1% and the investigation routing and approval time dropped from 2 to 3 days down to less than 1 day.
+800 HOURS PER YEAR SAVED
All the change records are at our fingertips now. Streamlined workflows improve the timeliness and overall change control process with CMOs.
Core Quality Processes
Quality Events
Digitize and connect quality events to quickly act on issues.
Nonconformance and Out of Specification
Manage and trend nonconforming product, investigations and approval of resulting actions and product dispositions.
Deviations
Manage deviations in a centralized location, with associated investigations, approvals and resulting records.
Corrective and Preventive Actions
Fully integrated CAPA system with automated routing, notification, delivery, escalation and approval capabilities.
Audit Management
An integrated tracking and workflow engine that automates audit findings, responses, corrective actions, approval and reporting.
Change Control
Manage changes from request, through pre-approvals, change execution, follow-up approvals and implementation.
Complaint Handling
Manage the entire complaint lifecycle, from investigation to resolution, and gain insights for continuous improvement.
Product Registration Tracking
Significantly reduce the time, cost and resources needed to track product submissions with regulatory agencies around the globe.
Check Out Other Honeywell Solutions
COMPLAINT MANAGEMENT SOFTWARE
The complaint handling QPA provides the ability to log, respond to and investigate complaints.
SUPPLIER QUALITY MANAGEMENT (SQM)
The supplier quality management QPA enables organizations to manage and collaborate with suppliers and contract manufacturers across your supply chain.
QUALITY RISK MANAGEMENT
Risk Management enables companies to seamlessly link the risk process to other quality management processes.
AUDIT MANAGEMEMT
The audit management QPA helps companies monitor critical processes, identify gaps and improve quality.
CORRECTIVE AND PREVENTIVE ACTION (CAPA)
The CAPA QPA enables organizations to track and manage the process of carrying out CAPA plans, automate verification of effectiveness over time, and provide seamless traceability to related quality processes, including change control and training.
NONCONFORMANCES
The nonconformance QPA records data about situations in which a product or device has not conformed to standards.
DOCUMENT MANAGEMENT
Access, edit, approve, store and share the latest version of quality documents throughout the value chain
TRAINING MANAGEMENT
With training management, automate company-wide training policies and regulatory requirements, where training activities are scheduled and tracked through completion
OUT OF SPECIFICATION
Document and track results of in-process or finished product testing falling out of specified limits using the Out of Specification (OOS) QPA.
CHANGE MANAGEMENT
The change management QPA manages change at every level of the supply chain to ensure quality and compliance requirements are not affected.
DEVIATIONS AND QUALITY EVENTS
Respond to adverse events faster with the quality events QPA and reduce the amount of time it takes to act on quality and safety issues.
