Lockbox QMS Quality Events Management

Enhance your Lab Operations by Tracking Quality Events from Creation to Closure

With Lockbox QMS Quality Events you can log deviations, Corrective and Preventive Actions (CAPAs), and occurrences all in one place. This quality event tracking system automates deviation and CAPA approval workflows and enables quality managers to track resolution time, evaluate impact, and assess risk for all quality events.

Streamline CAPA Management
Track Deviations in Real-Time
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Digitize Deviation and CAPA tracking

Use Lockbox QMS Quality Events to move away from paper-based tracking and start logging CAPAs, deviations, and occurrences in one central location.

Streamline CAPA Management

With Lockbox QMS, labs can track, investigate, review, and implement CAPAs, while tracking their effectiveness over time. The comprehensive reporting capabilities of Lockbox QMS enable users to see the status, progress, and resolution of quality events in real time.

View open/closed status and track the time taken to address and close each quality event
Track root causes and associate quality events to team members, procedures, samples, plates/batches, and reagents
Record target due date and verification method to evaluate if the CAPA was effective

Review and approve each component of a CAPA, including the description, plan, and closure
Connect one or more deviations to a CAPA
Automate and configure CAPA approval workflows
Easily connect CAPAs to the Lockbox QMS Document Control and Training modules

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Book a Demo – or –
Watch Recorded Webinar

Track Deviations in Real-Time

Lockbox QMS gives users the ability to track deviations and their root causes, as well as associate those deviations to a CAPA. Users maintain visibility into the status of the deviation and the time required to resolve it.

Classify deviations as planned or unplanned
Track time to resolve through automatic logging of the created date and approval date
Automatically route deviations to quality and lab managers for approval

See which team members have logged deviations and when they occurred
View team members, procedures, samples, plates/batches, and reagents associated with the deviation
Generate reports to track multiple deviations simultaneously