Change Management Software
See, understand, and manage every change appropriately within a fully traceable and centralized system.
Enhance change management processes with automation
SimplerQMS change management software system automates the change control processes. It enables you to automatically track changes, collect data, and send changes through the approval process. Furthermore, automatic notifications, follow-ups, and escalation of activities help to implement changes more effectively.
Changes to SOPs, instructions, products, and product processes automatically trigger tasks and sends email notifications to the appropriate personnel.
Easily link every change
With the SimplerQMS change management software system you can easily link objects, such as design control change records, nonconformances, risks, customer complaints, documents, CAPAs, and audits.
This gives you the ability to easily identify and manage exactly what was impacted by each change.
Enable end-to-end traceability
Our change management software solution allows for full traceability. You can see exactly what, when, by whom, and why changes were made, as well as the impact of that change.
SimplerQMS provides secure, FDA 21 CFR Part 11 compliant electronic signatures, time-stamped audit trails, and reporting capabilities allowing for full traceability of your quality documentation. Having such information readily available ensures compliance and makes you better prepared for audits.
Streamline your change control process
SimplerQMS allows you to easily identify non-compliant behavior and correct it before it escalates. With an integrated change management software system you can evaluate and manage what needs to be changed or updated.
No matter if the change was initiated due to a nonconformance, CAPA, or other issues, our fully integrated solution allows you to effectively manage the change process. Simply because all quality processes are connected and everything is stored in one centralized system.
Looking for more modules?
Regardless of the stage of your Life Science organization, our integrated software modules cover all your needs.
Save time with automated training activities, learning overview, reminders, and generation of training certificates.
Identify, uncover, resolve, and report all the preventative actions and corrective actions (CAPAs) seamlessly.
Reduce the associated risks and resolve issues quickly by optimizing complaint management processes.
Simplify your issue management workflows by automating tedious tasks.
Manage all the necessary processes related to product design and meet design control requirements with ease.
Automate and standardize your document control activities with ease.
Manage your equipment calibration schedule and automatically assigns tasks before due dates.
Sign and send the necessary documents for authoring, review, approval, from anywhere in the world, at any time.
Plan and organize all your product management activities and integrate them with other processes.
Automate your audit-related activities and ensure better audit preparedness.
Consolidate risk and handle your risk management file in a well-organized and structured manner.
Simplify supplier-related activities and handle your supplier documentation following the standards.
Standardize your documentation processes and boost employee productivity with effective document forms.
Streamline the investigation, documentation, and resolution of all your deviations.
Electronic Batch Records
Digitize and automate your batch record processes to ensure regulatory compliance.
Identify, evaluate, analyze and manage nonconformances more efficiently.
Trusted by companies around the world
Ready to learn more?
To learn how you can make the most of SimplerQMS, request a free, personalized demo presentation.