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.
Use Lockbox QMS Quality Events to move away from paper-based tracking and start logging CAPAs, deviations, and occurrences in one central location.
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.
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.
The Lockbox QMS Quality Events module is a quality event tracking system that lets you log deviations, Corrective and Preventive Actions (CAPAs), and occurrences all in one place. Instead of managing quality events on paper, you can track resolution time, evaluate impact, and assess risk from creation to closure in a single centralized system.
You can track deviations, CAPAs, and occurrences in Lockbox QMS, along with the details tied to each one — root causes, affected procedures, samples, plates/batches, reagents, and the team members involved. Centralizing this information gives you full visibility into every quality event across your lab.
The Lockbox QMS Quality Events module lets you track, investigate, review, and implement CAPAs while monitoring their effectiveness over time. You can record a target due date and verification method for each CAPA, review and approve each component — description, plan, and closure — and connect one or more deviations to a single CAPA.
Yes. The Lockbox QMS Quality Events module allows your Quality Team to configure automated CAPA approval workflows that match your laboratory’s review process. CAPAs are automatically routed to the appropriate reviewers and approvers before they can be closed.
The Lockbox QMS Quality Events module lets you log deviations in real time and classify them as planned or unplanned. You can track root causes, associate deviations with team members, procedures, samples, plates/batches, and reagents, and maintain full visibility into each deviation’s status as it moves toward resolution.
Yes. The Lockbox QMS Quality Events module automatically logs the created date and approval date for deviations, so you can track resolution time and identify where delays are occurring. This same visibility extends to CAPAs, giving you a clear view of open/closed status and time-to-close across all your quality events.
Yes. The Lockbox QMS Quality Events module can automatically route deviations to quality and lab managers for approval, helping you keep resolution moving without manual follow-up.
Yes. The Lockbox QMS Quality Events module keeps a record of which team members logged each deviation or CAPA and when it occurred, giving you accountability and traceability across your quality event history.
Yes. You can easily connect CAPAs to your Lockbox QMS Document Control module and Training Management module, making it simple to tie a corrective action to a revised SOP or the training your team completes as a result.
Yes. The Lockbox QMS Quality Events module offers comprehensive reporting so you can see the status, progress, and resolution of quality events in real time. You can generate reports to track multiple deviations simultaneously and monitor trends across your lab’s overall quality performance.
A quality event tracking system helps you move away from paper-based deviation and CAPA management, giving you real-time visibility into open items, root causes, and resolution times. By centralizing quality events in one place, you can respond to issues faster, demonstrate effective corrective action, and keep your lab audit-ready.
The Lockbox QMS Quality Events module helps laboratories support compliance with regulations and quality standards by providing configurable workflows, complete audit trails, electronic records, and controlled processes for managing deviations, nonconformances, CAPAs, and other quality events. These capabilities support laboratories working toward requirements such as 21 CFR Part 11, EU Annex 11, ISO 13485, ISO 17025, CAP/CLIA, GLP, and GMP.
