Top Free Quality Management Systems (QMS) - Page 4

Glartek

Glartek is an AI-native EHSQ software for industrial organisations working in high-risk sectors, including process manufacturing, energy and utilities, chemicals, food and beverage, and pharmaceuticals. Incident management, risk assessment, audits and inspections, environmental monitoring, contractor compliance, and corrective actions share a single data model, user experience, and AI layer. Glartek is built for the entire workforce, from field operators capturing data on a mobile device to EHS managers analysing trends and producing regulatory reports. The platform prioritises usability as a design principle, with an interface modern enough that adoption happens without intensive training programmes. When frontline teams use the system, EHS data improves, investigations become more accurate, and safety performance metrics move. AI is embedded in Glartek's operational workflows: it pre-fills incident and near-miss investigations from field-captured data, predicts the potential for serious injuries and fatalities using leading indicators, and guides operators through safety-critical tasks in real time. It is designed for the people on the ground, not just for back-office reporting. Glartek covers the full EHSQ scope: workplace safety, operational quality, environmental monitoring, occupational health, and contractor compliance. Capabilities include incident and near-miss management, risk assessment, permit-to-work, audit and inspection management, chemical management, corrective and preventive actions, environmental reporting, and a native mobile application with offline capability. The platform is no-code, requires no custom development, and is live within weeks. It supports full EHSQ deployments as well as phased adoption by module or operational area.

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icmInspector QMS

icmInspector QMS is a comprehensive digital platform designed to streamline and automate quality control processes across production, logistics, and service operations. It enables organizations to replace paper-based inspections with a fully digital workflow—collecting data directly from operators, machines, or IoT devices in real time. With icmInspector, companies can define inspection procedures, manage tasks, monitor results, and ensure compliance with internal standards or customer requirements. The system supports both web and mobile interfaces, making it ideal for use directly on the shop floor or in field inspections. The solution’s API allows seamless integration with ERP, MES, or other enterprise systems. Through standardized REST endpoints, icmInspector enables external systems to: - Authenticate and manage users and organizations, - Create and track inspection tasks, - Define and edit product definitions and parameters, - Collect and synchronize quality data from distributed sites, - Receive notifications about completed inspections or detected non-conformities. Each inspection form and result can be customized to reflect a company’s specific workflow, parameters, and reporting structure. The system offers full traceability of every action—from data entry to approval—ensuring transparency and audit readiness. Key benefits: - Digitized and standardized inspection workflows - Real-time access to inspection data and analytics - Automated task assignment and notifications - API integration with enterprise systems - Improved compliance, efficiency, and quality visibility Target users: Manufacturing, automotive, food production, logistics, and service companies seeking a scalable, data-driven approach to quality control. Company mission: Every better-made product or service changes the world for the better — and we help make that happen.

IMScollect

IMScollect is the integrated management system for ISO 9001, 14001 and 27001, with an AI advisor that knows your entire system and prepares everything. Documents, processes, risks, audits and actions are created once and reused across all standards. Built by auditors in Germany.

ISO 9001 CompliancePro

ISO 9001 CompliancePro is a monday.com-based solution from Simpleday Solutions that helps businesses organize and manage their ISO 9001:2015 implementation. The solution brings the main ISO 9001 processes, documentation, tasks, and records into one structured workspace in monday.com. This makes it easier for teams to see what needs to be done, keep documents organized, track progress, and manage the work involved in preparing for certification. The Complete Plan also includes 76 ISO 9001 document templates covering both mandatory and non-mandatory requirements. The templates are provided by Advisera and are available in monday Docs, Word, and Excel formats. Key features include: - Document management: Keep ISO 9001 documents organized in one place, with version control and change tracking. - Task and process management: Track implementation activities, responsibilities, deadlines, audits, and other QMS-related work. - Dashboards and reporting: Get a clear view of progress, open tasks, and key activities. - Automations: Use reminders and automated notifications to reduce manual follow-up. - Flexible workflows: Adapt the solution to your company's processes and how your team works. Simpleday also provides onboarding, training, and ongoing support. Depending on the plan, this includes an initial training session, monthly consultations, and email support. There are two plans available: ISO 9001 Basic Plan For companies that already have, or plan to create, their own ISO 9001 documentation. The plan provides the monday.com solution and support needed to organize and manage the implementation process. ISO 9001 Complete Plan For companies starting their ISO 9001 implementation and looking for both the monday.com solution and the documentation needed to get started. This plan includes 76 ISO 9001 templates, instructional videos, and expert guidance. Both plans include implementation of the solution in the company's monday.com account and initial training. A 14-day free trial is also available upon request, so companies can explore the solution before deciding whether it is the right fit.

Kapture.io

Kapture.io is a cloud-based Quality Management Software (QMS) designed to help organizations centralize, manage, and continuously improve their quality processes. Built around the Quality Circle, Kapture.io supports quality teams in creating a structured, repeatable approach to quality control and continuous improvement. The platform helps companies digitize and automate key quality management workflows such as audits, non-conformities, corrective and preventive actions (CAPA), , risk management and performance monitoring. By connecting these processes in one system, Kapture.io provides real-time visibility and make data-driven decisions. Kapture.io is designed to be flexible, scalable, and easy to adopt across industries where maintaining a strong quality management system is critical. By replacing manual workflows and disconnected tools, Kapture.io helps organizations standardize processes, improve collaboration, and continuously strengthen quality outcomes, closing the loop of the Quality Circle from planning to execution, verification, and improvement.

PDCA Software

PDCA Software is the comprehensive online solution that transforms scattered improvement ideas into measurable, actionable results. Whether you're implementing Kaizen methodologies, ensuring ISO 9001 compliance, or driving Total Quality Management (TQM) initiatives, our platform streamlines your entire improvement process. Your team is full of brilliant ideas, but how many get lost in emails, forgotten in meetings, or never make it past the suggestion box? PDCA Software provides a centralized improvement tracking system that captures every idea from your workforce and transforms them into structured improvement projects. Our intuitive interface makes it effortless for employees at all levels to contribute to your organization's growth, creating a true culture of continuous improvement. Built on the proven Plan-Do-Check-Act methodology, our software guides you through each phase of the improvement process. Create detailed improvement plans, track implementation progress, measure results, and standardize successful changes across your organization. With real-time analytics and reporting, you'll have complete visibility into your continuous improvement program's ROI and impact, ensuring every initiative drives meaningful results. Experience seamless improvement management with our mobile-optimized platform. Whether your team is in the office, on the production floor, or working remotely, PDCA Software ensures everyone can participate in your improvement culture. Our streamlined workflow minimizes administrative burden while maximizing participation and results, making improvement management accessible to organizations of any size. Support your quality management system with robust documentation, audit trails, and compliance reporting features. Perfect for organizations pursuing ISO certification or maintaining quality standards, PDCA Software provides the structure and accountability your improvement programs need to succeed. Transform your approach to operational excellence with systematic improvement tracking that delivers measurable outcomes. Join forward-thinking organizations already using PDCA Software to drive operational excellence. Experience the power of systematic improvement management with our 30-day free trial and discover how easy it can be to turn your improvement ideas into measurable results that transform your organization.

PQ-FMEA+

PQ-FMEA+ is an advanced and intuitive FMEA software for professional risk analysis and process optimization across PFMEA, DFMEA, MFMEA and SFMEA methodologies. It is fully compliant with AIAG, VDA and AIAG & VDA Edition 1 standards, supporting the creation of FMEA forms, Control Plans and Process Flow Diagrams within one connected environment. Unlike Excel-based tools, PQ-FMEA+ enables automatic data synchronization between all documents — FMEA Sheets, Control Plans and Flow Diagrams — ensuring full data consistency, version control and traceability. The system offers advanced functionality, including: built-in Risk Assessment Assistant for consistent O, S, D and AP evaluation, automatic generation of Control Plans and Process Flow Diagrams, version management and multi-level access structure, customizable templates and contextual hints for faster teamwork. PQ-FMEA+ is designed for organizations in the automotive, aerospace, electronics, medical and manufacturing sectors. It helps teams reduce analysis time by over 50%, eliminate manual errors and standardize documentation according to international quality standards. A free 30-day demo is available to explore all program features.

Prodle

Prodle AuditRoom is an An AI enabled unified audit workspace where auditors, suppliers, and stakeholders work seamlessly. Manage Documents • Meetings • Findings • Templates • Checklists • CAPA • Audit Reports , all in one workspace See Real results with : 50% faster audit turnaround time Remote audits for reduced costs & admin work AI tools for Improved audit accuracy Proactive detection of compliance gaps & risks Try it free: Contact sales@prodle.ai to schedule a demo or try the software

QMex

QMex is a comprehensive, modular Quality Management Software (QMS) designed to help organizations digitize, standardize, and continuously improve their quality and compliance processes. Built specifically for regulated industries such as pharmaceuticals, medical devices, chemicals, and manufacturing, QMex enables companies to manage complex quality workflows efficiently while ensuring full compliance with international standards and regulatory requirements. QMex centralizes all quality-related processes on a single, integrated platform. Core modules include - Document Management, - BMR Printout, - Change Control, - CAPA (Corrective and Preventive Actions), - Deviation and Nonconformance Management, - Customer Complaint, - Artwork, - Out of Limit, - Training Management, - Risk Management (FMEA), - Supplier Qualification, - Audit Management, - and Annual Product Review (APR / PQR). This modular structure allows organizations to start with their immediate needs and scale the system as their quality maturity grows. QMex supports end-to-end traceability and real-time visibility across quality processes. Advanced reporting and dashboard features provide actionable insights, helping organizations identify trends, mitigate risks proactively, and drive data-driven decision-making. Role-based access control, electronic signatures, and audit trails ensure data integrity and compliance with GMP, ISO 9001, ISO 13485, and other relevant regulations. Designed as a secure, cloud-ready enterprise solution, QMex integrates seamlessly with existing ERP, LMS, and production systems, enabling organizations to create a connected digital quality ecosystem. Its user-friendly interface improves adoption across departments, from quality assurance and production to regulatory affairs and management. By replacing fragmented systems and manual processes, QMex reduces operational risk, increases efficiency, and supports a culture of continuous improvement. Organizations using QMex benefit from improved compliance readiness, reduced audit preparation time, and enhanced collaboration across teams—making QMex a strategic solution for companies aiming to modernize and future-proof their quality management systems.

QM-Pilot

Q-Trust

Qredible’s product compliance management automation system Q-Trust is purpose built for regulated industries like CBD, nutraceuticals, hemp, wellness supplements, peptides, alkaloids, kratom, functional mushrooms, and cannabis. Q-Trust's digital registry is a centralized source of truth for your regulated business containing your business licenses, critical federal and state compliance documents, COAs and more secured by blockchain. This automated product compliance management tool and merchant monitoring solution connects your entire supply chain through efficient digital commerce building trust with financial partners, merchant processors, regulators, and your customers. Q-Trust’s suite of integrated modules includes: Q-Transact™ is an enterprise and omni-channel digital commerce and supply chain solution for compliance-driven commerce and operations. Q-Transact is a licensable platform within Q-Trust designed to support regulated products sold through retail, wholesale, affiliate, and multilevel marketing enterprises. The platform leverages advanced features to ensure compliance with existing and emerging regulations: • Built-in compliance functionality • Real-time, continuous monitoring and alerting • Automated data access for integrated merchant processing partners • Q-Trust and Q-Monitor integration • Industry-specific focus • Transparent content management • Sales tax management The Q-Monitor function within the Q-Trust platform is designed to enable the efficient tracking, monitoring, and management of counter-party risk. Q-Monitor is a cutting-edge risk management and merchant monitoring solution that combines multiple microservices to provide comprehensive compliance and reputation monitoring. This powerful suite offers automated compliance checks, SOP management, employee training tracking, and reputation monitoring using AI-driven web crawlers. It also includes product compliance reviews, content monitoring for regulatory adherence, and automated KYC processes for financial institutions. With its intelligent alerting system, Q-Monitor enables businesses to proactively identify and address potential regulatory issues in real-time. By integrating these advanced features, Q-Monitor empowers companies to efficiently manage risks, maintain compliance, and safeguard their reputation in highly regulated industries. The Q-Vault module is a Blockchain-Based Document Management Module: Built on Hyperledger Fabric, this microservice module offers a secure and efficient solution for managing critical documents in regulated, compliance driven industries. This module enables seamless review, annotation, workflow management, and immutable storage of essential documents. Leveraging smart contracts for automated workflows, the system ensures compliance, provides robust access control, and facilitates real-time collaboration. With features like tamper-proof storage, comprehensive audit trails, and integration capabilities, it enhances security, improves compliance, increases efficiency, and reduces costs. Q-Verify™ delivers end-to-end verification that reduces fraud and lowers compliance costs while providing financial institutions the confidence they need to maintain your services without disruption. You start by validating your company's good standing, required licenses, and regulatory compliance status to establish fundamental legitimacy with financial partners and regulators. The next step confirms your website, social media content, and reputation platforms maintain compliance with FDA, FTC, and state regulatory standards for transparent, compliant communication. Next escalation secures your product COAs with blockchain technology, validates compliance with current regulations, and ensures proper labeling for complete product integrity. The last verification level certifies that your sales channels implement proper age verification, regional sales restrictions, and maintain compliant payment processing relationships for secure transactions. MyCOA® - Certificate of Analysis software: Automates the reception, distribution, and approval of Certificates of Analysis and writes into the Blockchain creating a smart contract ID, ensuring product quality and transparency across the supply chain. Enables COAs to be displayed through a customer friendly modal that can be integrated into your website, point-of-sale, product catalogs, etc. Quick and easy access to lab reports is provided through QR Code integration and the ability to find COA’s based on lot and batch numbers and/or UPC codes found on products. Q-Comply - AI Compliance Module: Qredible's AI-powered Compliance Tracker and Interpreter revolutionizes regulatory compliance in regulated product industries. This innovative tool harnesses advanced natural language processing and machine learning algorithms to continuously monitor, analyze, and interpret complex regulations across various jurisdictions. It distills intricate legal jargon into clear, concise narratives, making compliance accessible to all stakeholders. The system provides real-time updates on regulatory changes, offers customized compliance recommendations, and generates easy-to-understand explanations of key regulations. By simplifying the compliance landscape, this AI-driven solution enables companies to quickly grasp and adapt to regulatory requirements, reducing risk and ensuring adherence to ever-evolving industry standards.

QualiHQ

QualiHQ: Quality Management System for Early-Stage SaaS and Digital Health Teams QualiHQ is a Quality Management System (QMS) designed for small software teams building products in regulated healthcare environments. It is intended for founders and early-stage companies that need to implement structured quality and compliance processes but may not have dedicated regulatory or quality assurance resources. While software development has become faster and more accessible, regulatory requirements for healthcare products—such as Software as a Medical Device (SaMD)—remain complex and documentation-heavy. Many existing QMS platforms are designed for larger organizations and assume prior knowledge of regulatory standards. QualiHQ focuses on providing a more accessible starting point for teams that are new to compliance. The platform includes guided onboarding to introduce key regulatory concepts and requirements as users set up their system. Instead of requiring full documentation upfront, QualiHQ supports incremental progress, allowing teams to build their quality system alongside product development. QualiHQ also incorporates AI-assisted features to help generate initial drafts of required documentation based on user inputs about their product and processes. These drafts are intended to reduce the effort associated with starting documentation from scratch, while still requiring review and validation by the user. The system is structured to align with common expectations for regulated healthcare software, including document control, process definition, and traceability. It is not limited to a specific regulatory framework but is intended to support teams working toward compliance with standards such as ISO 13485 or similar requirements. QualiHQ is typically used by early-stage SaMD startups, digital health founders, and small teams entering regulated markets. It may also be relevant for software teams that need to introduce lightweight quality processes without adopting a full enterprise QMS solution. Categories: Regulatory Technology, Healthcare IT, Quality Management Software (QMS), eQMS Typical users: SaMD startups, digital health companies, early-stage medtech teams, and small SaaS teams working in regulated environments

QwizPRO

QwizPRO simplifies quality management for ISO 9001 and AS9100 compliance, ensuring stress-free audits. Its user-friendly automation minimizes errors, saves time, and streamlines the compliance process. QwizPRO is an essential for today’s competitive business environment, enabling quality excellence that’s hassle-free.

Siemens QMS Solution

Siemens QMS is a comprehensive solution native in Teamcenter and Opcenter X platforms, delivering seamless quality and compliance management across the product lifecycle and manufacturing operations. Built on a modular, scalable architecture, it provides core capabilities such as Corrective and Preventive Actions (CAPA), Supplier Quality Management, Audit Management, Document Control, Training and Qualification Management. Moreover, Siemens QMS solution supports advanced processes including Risk Management/FMEA, APQP and PPAP, Model-based Characteristics, Variation Analysis, Measurement System Analysis, Inspection Management, SPC, Analytics, Non-Conformance and Quality Action Management, enabling end-to-end quality across the product lifecycle. By aligning with standards like ISO 9001 and leveraging AI features, Siemens QMS empowers manufacturers to enhance efficiency, mitigate risk and foster a culture of continuous improvement to achieve excellence in quality and compliance across industries.

SmartAPQP

SmartAPQP connects APQP, FMEA, Control Plan, PPAP, RFQ, BOM/ECN, CAPA and supplier collaboration on one Part Master — built for IATF 16949 manufacturers.