Product Lifecycle Management Software
Digitize product management processes and expand your product portfolio with ease.
Maintain a complete and compliant product documentation
SimplerQMS product lifecycle management (PLM) software solution helps you manage your product-related documentation effectively. All records and approvals, for a specific product, with versioning, audit trail, and electronic signatures, can easily be found in one cloud location.
Automate your product management activities
With SimplerQMS, you can automate data collection, routing, notifications, follow-ups, approvals, and escalation of product-related activities.
Our automated workflows ensure that the relevant personnel is always notified when they are assigned a specific task. You can easily track everyone’s performance towards their due dates through customizable Dashboards and Notifications, allowing you to gain an overview of your product documentation status.
Product and Components Handling in Action
Link all relevant files to a chosen product and enjoy easier compliance. In this video, we uncover how SimplerQMS relates components and documents to a specific product with a variety of options for documentation.
Streamline compliance with product management activities
SimplerQMS product lifecycle management (PLM) software solution provides secure, FDA 21 CFR Part 11 compliant electronic signatures, time-stamped audit trails, and reporting capabilities allowing for full traceability.
This means that you can easily see exactly what, when, by whom, and why changes were made, as well as the impact of that product record change. Having such information readily available ensures compliance and makes you better prepared for audits.
Integrate data across other quality processes
With SimplerQMS, you can easily link production records with other related documents, for example, electronic batch records (EBR), device master records (DMR), audits, or inspection reports.
Seamlessly upload and link any document, file, record, and email to an audit, risk, and CAPA, as evidence, and store everything in a single location. This way you will gain better visibility, easily identify non-compliant behavior and correct it before it escalates.
Maintain product-related components
Easily maintain components and their relations to products.
Link components to external vendors or suppliers, to maintain traceability of your supply chain processes.
Looking for more modules?
Regardless of the stage of your Life Science organization, our integrated software modules cover all your needs.
Training Management
Save time with automated training activities, learning overview, reminders, and generation of training certificates.
CAPA Management
Identify, uncover, resolve, and report all the preventative actions and corrective actions (CAPAs) seamlessly.
Complaint Management
Reduce the associated risks and resolve issues quickly by optimizing complaint management processes.
Change Management
Recognize and manage all changes accordingly to ensure compliance and structure within your organization’s QMS.
Design Control
Manage all the necessary processes related to product design and meet design control requirements with ease.
Document Control
Automate and standardize your document control activities with ease.
Equipment Calibration
Manage your equipment calibration schedule and automatically assigns tasks before due dates.
Electronic Signatures
Sign and send the necessary documents for authoring, review, approval, from anywhere in the world, at any time.
Issue Management
Simplify your issue management workflows by automating tedious tasks.
Audit Management
Automate your audit-related activities and ensure better audit preparedness.
Risk Management
Consolidate risk and handle your risk management file in a well-organized and structured manner.
Supplier Management
Simplify supplier-related activities and handle your supplier documentation following the standards.
Form Management
Standardize your documentation processes and boost employee productivity with effective document forms.
Deviation Management
Streamline the investigation, documentation, and resolution of all your deviations.
Electronic Batch Records
Digitize and automate your batch record processes to ensure regulatory compliance.
Nonconformance Management
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.
