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description: Page 22 - See the top Quality Management Software solutions in Ireland. Capterra offers software reviews, prices, and features helping you find the best software for your business needs.
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title: Page 22 - Quality Management Software - Prices & Reviews - Capterra Ireland
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Breadcrumb: [Home](/) > [Quality Management Software](https://www.capterra.ie/directory/30099/quality-management/software) > [Page 22](https://www.capterra.ie/directory/30099/quality-management/software?page=22)

# Quality Management Software

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> Quality Management software automates the process of tracking and minimizing product defects.

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## Products

1. [QHSE](https://www.capterra.ie/software/1073205/QHSE) (0 reviews) — FullyInControl offers a QHSE management software that helps businesses with streamlining compliance and operational risk programs.
2. [NORMEX](https://www.capterra.ie/software/1074269/NORMEX) (0 reviews) — Normex is a food safety management solution that provides traceability and compliance tools to help food businesses meet regulations.
3. [MS Frog](https://www.capterra.ie/software/1074289/MS-Frog) (0 reviews) — MS Frog offers a clear, step-by-step path to building, running, and auditing your ISO system. Built by ISO Lead Auditors.
4. [DL QualityCore](https://www.capterra.ie/software/1074962/DL-QualityCore) (0 reviews) — DL QualityCore combines powerful document control with automation to meet ISO and other regulatory requirements faster and easier.
5. [Metaware](https://www.capterra.ie/software/1076047/Metaware) (0 reviews) — Metaware.nl is cloud-based QMS \&amp; GRC software supporting ISO standards, centralising compliance, risk and audits for improvement.
6. [CIPA](https://www.capterra.ie/software/1076086/CIPA) (0 reviews) — AI-enabled tool that assists with audit digitalization, incident and event reporting, quality management, and action plan management.
7. [OpsAssist](https://www.capterra.ie/software/1077677/OpsAssist) (0 reviews) — Anvil is a nuclear-focused quality management and compliance automation platform designed to make regulated operations audit-ready.
8. [sterloCare](https://www.capterra.ie/software/1078201/sterloCare) (0 reviews) — sterloCare is healthcare software that digitizes hospital operations, improves patient experience, and ensures regulatory compliance.
9. [ELIZA](https://www.capterra.ie/software/1078311/ELIZA) (0 reviews) — ELIZA is a cloud-based software that helps streamline quality management, process digitization, and HR functions for businesses.
10. [QMS Total](https://www.capterra.ie/software/1078682/QMS-Total) (0 reviews) — Laboratory quality management tool that streamlines operations, tracks records and documents, and supports ISO/IEC 17025 compliance.
11. [Ellistat IQC](https://www.capterra.ie/software/1078772/Ellistat-IQC) (0 reviews) — Control and improve batch quality according to ISO standards (ISO 2859, ISO 3951 or others) with Ellistat's incoming quality control.
12. [CorrectTrack](https://www.capterra.ie/software/206608/correcttrack) (0 reviews) — CorrectTrack is a software for monitoring customer satisfaction, environmental performance, and employee health and safety.
13. [foodflou](https://www.capterra.ie/software/1082439/foodflou) (0 reviews) — foodflou is compliance software for food manufacturing that automates regulations, reduces safety risks, and ensures audit readiness.
14. [PaperLess GMP](https://www.capterra.ie/software/1082699/PaperLess-GMP) (0 reviews) — Pharma Manufacturing ERP tool that provides compliance with 21 CFR Part 11 regulations, time and audit management features, and more.
15. [Allera](https://www.capterra.ie/software/1082700/Allera) (0 reviews) — Allera offers a compliance software to streamline supplier management, document control, and food safety processes.
16. [PvEdge](https://www.capterra.ie/software/1050834/pvedge) (0 reviews) — PvEdge is pharmacovigilance software automating case processing, signal detection, and literature intake for drug safety compliance.
17. [GoSmarter](https://www.capterra.ie/software/1083901/GoSmarter) (0 reviews) — Cloud-based and AI-enabled software for metals manufacturers to streamline operations, enhance compliance, and more with automation.
18. [QM.Pro 365](https://www.capterra.ie/software/1084316/QM-Pro-365) (0 reviews) — Quality management solution that helps businesses integrate the system with Microsoft 365 to standardize processes \&amp; ensure compliance.
19. [QSEH Star](https://www.capterra.ie/software/1086035/QSEH-Star) (0 reviews) — Quality management solution that helps businesses manage complaints, inspections, incidents, claims, deviations, and certifications.
20. [eLeaP Quality Management System (QMS)](https://www.capterra.ie/software/1086100/eLeaP-Quality-Management-System-QMS) (0 reviews) — eLeaP QMS software integrates document control, risk, change, supplier, and learning management to ensure audit readiness.
21. [ShareMe QMS](https://www.capterra.ie/software/1091466/ShareMe-QMS) (0 reviews) — Quality management solution built on Microsoft 365 that helps regulated industries automate and control quality processes.
22. [BizPortals QCFlow](https://www.capterra.ie/software/1091578/BizPortals-QCFlow) (0 reviews) — Quality management solution that helps enterprises manage quality, compliance, audits, risk, and more using a unified interface.
23. [BrixIQ](https://www.capterra.ie/software/1092334/BrixIQ) (0 reviews) — BrixIQ is AI-driven quality assurance software that unifies quality data to help manufacturers respond faster and stay audit-ready.

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## Related Categories

- [EHS Management Software](https://www.capterra.ie/directory/10015/ehs-management/software)
- [Document Control Software](https://www.capterra.ie/directory/31197/document-control/software)
- [Risk Management Software](https://www.capterra.ie/directory/30665/risk-management/software)
- [Document Management Software](https://www.capterra.ie/directory/30063/document-management/software)
- [Audit Software](https://www.capterra.ie/directory/30664/audit/software)

## Links

- [View on Capterra](https://www.capterra.ie/directory/30099/quality-management/software)
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-----

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Built on the proven Document Locator platform, it combines powerful document control with intuitive workflows designed to achieve and meet ISO and other regulatory requirements faster and easier. Whether you’re managing records, CAPAs, Non-Conformities, Training, Audits, or more, DL QualityCore eliminates paper-based headaches and manual tracking. \n\nCapabilities\n- Document Control: Version control, secure access, reporting\n- NCR & CAR: Track corrective actions and identify, record, and resolve issues\n- Training Records: Automate required reading and track employee certifications\n- Audit Management: Simplify audits with accurate, up-to-date records\n- ISO Ready: Pre-configured to align with ISO requirements\n- Powerful Reporting: Track your ISO records\n- Quick Deployment: Get up and running in weeks, not months\n- Easy to use: Familiar folder-and-file based interface","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/24774e26-5d27-4ca9-9d44-532cde51eebc.png","url":"https://www.capterra.ie/software/1074962/DL-QualityCore","@type":"ListItem"},{"name":"Metaware","position":5,"description":"Metaware.nl is a modern, scalable quality management software platform that helps organizations implement, manage and continuously improve their Quality Management System (QMS or GRC). The platform fully supports ISO 9001, ISO 14001, ISO 27001 and other international standards, enabling organizations to demonstrably comply with laws, regulations and certification requirements. Metaware centralizes document control, process management, risk management, incident and complaint management, CAPA, internal audits and management reviews in one secure, cloud-based sovereign solution. With real-time dashboards, workflow automation, role-based access and version control, organizations gain full control over quality, compliance and operational performance. 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The platform also leverages AI to uncover insights and opportunities to optimize quality management and continuous improvement processes.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/d7157ecf-4165-4604-b220-b40c9102f9cb.png","url":"https://www.capterra.ie/software/1076086/CIPA","@type":"ListItem"},{"name":"OpsAssist","position":7,"description":"Anvil (by Forged Operations) is a nuclear-focused quality management and compliance automation platform designed to make regulated operations audit-ready by default. It centralizes controlled documentation and quality records, enforces role-based workflows (including corrective actions such as NCR/CAR), and supports training/qualification management and evidence traceability across suppliers and operators.\n\nAnvil has AI-assisted audit acceleration capabilities to reduce manual effort in preparing for and executing audits, such as organizing large procedure/evidence sets, mapping procedure sections to checklist clauses, linking supporting evidence to requirements, and performing automated checks against procedure rules.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/0d3c7cc7-62fc-4b90-9563-eb4e48e0c877.png","url":"https://www.capterra.ie/software/1077677/OpsAssist","@type":"ListItem"},{"name":"sterloCare","position":8,"description":"sterloCare is a healthcare digitization software that enhances patient satisfaction while ensuring compliance with NABH standards. The platform features QR code-based patient support systems for service requests, complaint management, and feedback collection, along with digital token systems for tracking outpatient journeys and reducing wait times. SterloCare includes modules for patient experience management, quality control, and performance monitoring through customizable dashboards and reports that facilitate data-driven decision making. The software supports both cloud and on-premise deployment with multilingual capabilities, role-based workflows, and automated notifications via mobile and email. sterloCare integrates with existing hospital information systems to improve operational efficiency and provides customizable dashboards for monitoring key metrics across departments.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/d9122d6a-628a-4d14-bbe3-ac88ea8ef75b.jpeg","url":"https://www.capterra.ie/software/1078201/sterloCare","@type":"ListItem"},{"name":"ELIZA","position":9,"description":"ELIZA is a cloud-based management software that streamlines quality management, process digitization, and organizational leadership. The platform consists of three main modules: ELIZA QM for quality management processes, ELIZA HR for personnel management with electronic employee files, and ELIZA CxO for integrated management systems. The software includes process management tools, risk assessment capabilities, contract administration, project portfolio management, and ISO 9001 compliance functionality. ELIZA features document management, continuous improvement processes, meeting management, and task tracking. The web-based interface works across desktop and mobile devices, allowing organizations to centralize management information, simplify compliance requirements, and digitize workflows. The system integrates with existing IT environments through open interfaces and supports data exchange with various systems including Microsoft environments.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/c96b87aa-fc86-4a80-8714-0989016d0ebb.jpeg","url":"https://www.capterra.ie/software/1078311/ELIZA","@type":"ListItem"},{"name":"QMS Total","position":10,"description":"Laboratory quality management system software designed to help laboratories achieve ISO/IEC 17025 compliance. The system features centralized document control, audit readiness, non-conformance tracking, employee training records management, and risk management modules. QMS Total includes specialized components for equipment calibration management with automated scheduling, equipment inventory tracking, and digital calibration certificates. The system enables laboratories to streamline compliance processes and maintain quality standards across operations through its document management and quality control features.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/5ee68ab0-07ba-4910-ab1f-6fed479de9b2.webp","url":"https://www.capterra.ie/software/1078682/QMS-Total","@type":"ListItem"},{"name":"Ellistat IQC","position":11,"description":"Ellistat IQC is quality control software designed to optimize incoming inspections while adhering to ISO 2859 and ISO 3951 standards. It dynamically adjusts inspection levels based on supplier lot quality history, balancing quality assurance with efficiency. Supporting both attribute-based and variable-based sampling methods, it offers customizable plans to meet specific needs.\n\nThe software integrates with measurement devices via USB, Bluetooth, or RS232, eliminating manual data entry errors and ensuring traceability. Measurement data is automatically recorded for comprehensive tracking of inspection results.\n\nEllistat IQC features an intuitive interface, customizable dashboards, and detailed analytical reports. Accessible across devices, it includes an API for integration with MES, ERP, and other systems, streamlining quality control processes while maintaining high standards.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/462d0bce-6590-4875-bffb-2e73c314fc46.png","url":"https://www.capterra.ie/software/1078772/Ellistat-IQC","@type":"ListItem"},{"name":"CorrectTrack","position":12,"description":"CorrectTrack is a workflow and management software for environmental, health, and safety (EHS) risk management. It centralizes the identification, analysis, and control of risks related to customer satisfaction, environmental performance, and employee safety. The software supports EHS audits by tracking corrective actions and providing evidence of risk control measures. Its open architecture enables integration with other systems for customization. CorrectTrack features a risk analysis module to help safety teams identify opportunities and develop solutions. Users can assign corrective actions, create permission-based workflows, monitor task status, and generate performance dashboards. With a user-friendly interface, scalable features, and tutorials, CorrectTrack improves EHS performance through centralized risk management.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/469422c3-7c2a-4381-94ed-3a83ebd1ae01.jpeg","url":"https://www.capterra.ie/software/206608/correcttrack","@type":"ListItem"},{"name":"foodflou","position":13,"description":"foodflou is an AI-driven quality management software for the food manufacturing industry, designed to streamline compliance, reduce safety risks, and ensure audit readiness. It offers smart document control with version tracking, comprehensive supplier management, customizable audits, centralized complaint reporting, and integrated corrective action management. The Foody AI assistant provides real-time updates and alerts for efficient workflows.\n\nfoodflou unifies data, teams, and compliance efforts into a customizable platform adaptable to various food production processes. Teams can personalize forms, inspections, and workflows to meet specific needs. With features like action logging for traceability, task calendars, and integrated document editing, foodflou reduces manual work, shortens audit preparation time, and speeds up market readiness. The platform supports food safety teams of all sizes in staying organized and managing potential risks effectively.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/c0b80d99-d093-4152-b7e6-492630096eee.jpg","url":"https://www.capterra.ie/software/1082439/foodflou","@type":"ListItem"},{"name":"PaperLess GMP","position":14,"description":"Digital documentation system for pharmaceutical manufacturing compliance, streamlining quality processes and regulatory adherence. Key features include electronic batch manufacturing records (eBMR/eBPR), quality management, training management, and document control. It integrates with laboratory information management systems, manufacturing execution systems, and ERP platforms for full operational traceability.  It ensures consistent documentation practices and readiness for regulatory inspections.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/a5ebfda2-4098-4666-870a-739a2402d10b.jpeg","url":"https://www.capterra.ie/software/1082699/PaperLess-GMP","@type":"ListItem"},{"name":"Allera","position":15,"description":"Allera is a food safety and quality management software that streamlines compliance, reporting, supplier management, and document control. The platform simplifies operations, reduces risks, and ensures food safety. The system features document control functionality that allows users to manage SOPs, track revisions, and handle approvals while offering AI-powered suggestions to enhance documentation. \n\nAutomated supplier management eliminates manual tracking through dynamic forms with conditional logic and timestamps, ensuring complete and timely submissions. Allera helps organizations transition to paperless operations by replacing physical binders and clipboards with digital forms that are searchable, and audit-ready. The platform includes analytics capabilities that support maintaining high standards of safety and quality while minimizing operational risks.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/4d38e749-6ce8-4c2b-bb51-b6e159ee8771.jpg","url":"https://www.capterra.ie/software/1082700/Allera","@type":"ListItem"},{"name":"PvEdge","position":16,"description":"PvEdge is a pharmacovigilance software solution that automates critical safety management processes for drugs, devices, vaccines, and combination products. It integrates seamlessly with a Drug Safety Database, ensuring efficiency and accuracy in monitoring pharmaceutical data. The Multisource Inbox and Triage tool streamlines case processing by segregating relevant information from multiple sources. The Literature Automation module extracts safety data quickly, enabling real-time analysis and proactive risk assessment. PvEdge automates document workflows for reports like PADERs, ensuring compliance with global regulations. Additional features include ICSR Submissions for global case submissions and Automated Signal Detection that identifies potential risks using advanced algorithms. PvEdge delivers an integrated solution that simplifies drug safety management while maintaining high standards for patient safety.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/acb632de-c21e-47d3-8da3-141753c28d69.png","url":"https://www.capterra.ie/software/1050834/pvedge","@type":"ListItem"},{"name":"GoSmarter","position":17,"description":"Cloud-based and AI-powered assistant for metals manufacturing, designed to streamline operations and compliance requirements through automation. It digitizes and manages mill certificates and Material Test Reports (MTRs). The platform tracks product journeys and integrates seamlessly with existing systems. Using AI algorithms, GoSmarter optimizes production planning. Compliance management is automated, eliminating the need for manual processes. It automates routine tasks and provides actionable insights, transforming document-heavy workflows.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/5ba68f47-8d7f-4c28-a7ce-5e0c13dcd2cf.png","url":"https://www.capterra.ie/software/1083901/GoSmarter","@type":"ListItem"},{"name":"QM.Pro 365","position":18,"description":"QM.Pro 365 is a quality management solution integrated with Microsoft 365, including SharePoint, MS Teams, and Power Automate. It enables teams to streamline processes by eliminating data silos and enabling users to work within familiar Microsoft tools.\n\nThe system ensures compliance with ISO standards through document management, version control, and approval workflows. With intelligent search, automated workflows, and process visualization, QM.Pro 365 lets stakeholders simplify quality management. \n\nIt allows operators to keep all data within the customer’s Microsoft 365 environment, ensuring security and control. The platform supports multilingual operations, features dashboards for monitoring quality metrics, and uses AI for context-aware searches, delivering precise answers.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/0af7d49e-eb0b-4671-a711-bf9bedc38e73.jpg","url":"https://www.capterra.ie/software/1084316/QM-Pro-365","@type":"ListItem"},{"name":"QSEH Star","position":19,"description":"QSEH Star is quality management solution that helps businesses digitize workflows for quality, safety, environment, and health processes. It offers various customizable modules, including quality control, risk assessment, incident reporting, and environmental monitoring, all configurable to meet operational needs.\n\nThe modular structure lets organizations select and scale modules, ensuring flexibility and consistency across functions. With real-time data access, teams can track actions, monitor compliance, and analyze case relationships effectively. \n\nRegular updates every two weeks introduce new features, ensuring the solution evolves to meet emerging requirements. Centralized documentation enhances transparency, while action tracking and follow-ups support efficient management of quality, safety, environmental, and health initiatives.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/18a2fbaa-4058-4d85-b4d8-826dbb3359d2.png","url":"https://www.capterra.ie/software/1086035/QSEH-Star","@type":"ListItem"},{"name":"eLeaP Quality Management System (QMS)","position":20,"description":"eLeaP Quality Management System (QMS) integrates enterprise learning management with quality processes like document control, design controls, risk management, change control, and supplier management. It includes modules for 21 CFR Part 11-compliant document management, ISO 13485 design controls, ISO 14971 risk management, supplier audits, and CAPA tracking. The validated LMS ensures audits or changes trigger retraining and competency checks, while approved documents deploy training assignments automatically. Design changes cascade to personnel for competency assessments, and risk mitigation links to mandatory training. Pre-validated for life sciences, eLeaP supports 21 CFR Part 820, ISO 13485, and EU MDR compliance, offering audit trails and real-time visibility. It serves medical device manufacturers, pharmaceutical firms, biotech companies, and clinical research organizations focused on audit readiness.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/27fcca4c-c667-4e93-92ae-b32b5091b937.jpeg","url":"https://www.capterra.ie/software/1086100/eLeaP-Quality-Management-System-QMS","@type":"ListItem"},{"name":"ShareMe QMS","position":21,"description":"ShareMe QMS is a quality management and document control solution that helps businesses automate processes while ensuring compliance with regulatory standards. It enables teams to manage document control, non-conformities, CAPA, change control, audits, training, and equipment tracking. Built on Microsoft 365 and SharePoint Online, it operates via a web browser without local installation.\n\nThe modular design allows organizations to expand functionality as needed. With GMP validation capabilities, ShareMe QMS suits industries with strict regulations. The cloud-based platform enables access from multiple devices, supporting remote collaboration. Users can customize workflows to meet specific requirements.\n\nShareMe QMS supports compliance with FDA 21 CFR Part 11, ISO standards, and GMP guidelines. It also manages customer and supplier documentation, bulletin control, and audit scheduling.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/74a99821-5da0-42ec-baf2-b6e8a31a3953.jpg","url":"https://www.capterra.ie/software/1091466/ShareMe-QMS","@type":"ListItem"},{"name":"BizPortals QCFlow","position":22,"description":"BizPortals QCFlow is a cloud-based quality management system that helps businesses centralize quality, compliance, audits, and risk on a single configurable platform. It replaces fragmented tools with a unified approach to quality execution and compliance control. Configurable workflows ensure scalability, while multi-site architecture maintains consistent quality across global locations and reduces IT overhead.\n\nThe platform centralizes procedures, policies, approvals, and audit evidence, with compliance templates and secure electronic signatures ensuring traceability. Integrated risk, issue, and corrective action management supports defect tracking, root cause analysis, and automated workflows. Real-time dashboards and trend analysis enable proactive decision-making, while integration with manufacturing systems, CRM platforms, and mobile tools extends functionality. BizPortals QCFlow aligns with standards like GMP, ISO 9001, and IEC 27001 for audit readiness.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/b8bb2bc5-eda4-45c6-9ffa-f3bdf5c8b7da.png","url":"https://www.capterra.ie/software/1091578/BizPortals-QCFlow","@type":"ListItem"},{"name":"BrixIQ","position":23,"description":"BrixIQ is an AI-driven quality assurance platform that unifies scattered quality data from emails, PDFs, spreadsheets, and other systems into a single platform. This centralization eliminates the need to search through disconnected systems, enabling faster customer response times by resolving issues in hours instead of days. The automated case management system reduces task sorting from hours to minutes. The platform includes AI-powered document search, smart scanning with auto-tagging, SPC alerts for process monitoring, and integration with ERP/MRP systems. BrixIQ keeps documentation organized and enables instant report generation to maintain audit readiness. The system connects all quality information sources to provide immediate access to data when needed. By unifying data and automating processes, BrixIQ helps manufacturers address quality issues more efficiently while maintaining organized compliance documentation.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/3bdc0cd9-7e2b-4ae7-b861-bc5e36a5ad41.jpg","url":"https://www.capterra.ie/software/1092334/BrixIQ","@type":"ListItem"}],"numberOfItems":23}
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