# Top Free Quality Management Systems (QMS) - Page 4 ## How Many Quality Management Systems (QMS) Products Does G2 Track? **Total Products under this Category:** 232 ### Category Stats (Jul 2026) - **Average Rating:** 4.42/5 The average rating of products in this category, based on all submitted ratings - **Top Trending Product:** Q-Hub (+5.56%) - Among all products in this category, Q-Hub recorded the largest rating increase compared to last month _Last updated: July 31, 2026_ ## How Does G2 Rank Quality Management Systems (QMS) Products? **Why You Can Trust G2's Software Rankings:** - 30 Analysts and Data Experts - 9,300+ Authentic Reviews - 232+ Products - Unbiased Rankings G2's software rankings are built on verified user reviews, rigorous moderation, and a consistent research methodology maintained by a team of analysts and data experts. Each product is measured using the same transparent criteria, with no paid placement or vendor influence. While reviews reflect real user experiences, which can be subjective, they offer valuable insight into how software performs in the hands of professionals. Together, these inputs power the G2 Score, a standardized way to compare tools within every category. ## G2 Grid® for Quality Management Systems (QMS) ![G2 Grid® for Quality Management Systems (QMS) plotting products by satisfaction and market presence](https://www.g2.com/categories/quality-management-qms/grids.png?focus%5B%5D=18510&focus%5B%5D=4169&focus%5B%5D=142380&focus%5B%5D=40484&focus%5B%5D=39899&focus%5B%5D=50982&focus%5B%5D=54666&focus%5B%5D=19175) Highlighted products: MasterControl Quality Management System, Qualio, Redzone, EASE, Octave Reliance (ETQ Reliance), QT9 QMS, SafetyCulture, and SAP Cloud ERP (SAP S/4HANA Cloud). Underlying data: [Grid® JSON](https://www.g2.com/categories/quality-management-qms/grids.json?focus%5B%5D=mastercontrol-quality-management-system&focus%5B%5D=qualio&focus%5B%5D=qad-redzone&focus%5B%5D=ease-inc-ease&focus%5B%5D=octave-reliance-etq-reliance&focus%5B%5D=qt9-qms&focus%5B%5D=safetyculturehq&focus%5B%5D=sap-cloud-erp-sap-s-4hana-cloud) **Sponsored** ### Greenlight Guru Quality Management System Greenlight Guru is the #1 quality management system built exclusively for medical device companies. Not life sciences. Not pharma with a medtech configuration layer. Because we built exclusively for medical devices, ISO 13485, ISO 14971, and FDA QMSR aren't frameworks you configure after the fact. They're the foundation. Most quality teams manage compliance across systems that were never designed to talk to each other. A document control tool here, a spreadsheet for CAPAs there, a separate process for change control. In a regulated environment, that gap doesn't stay invisible, it shows up during audits. Greenlight Guru gives Quality and Product teams a single connected system where document control, training, CAPA, nonconformance, change control, supplier management, risk management, and design controls work together. When a change happens, it flows through the workflow. Meaning limited manual handoffs, and nothing falling through the cracks between teams. For Quality and Regulatory Affairs professionals, that means audit-ready workflows with automated routing, electronic signatures, and complete audit trails built in, including end-to-end traceability across design controls. No more chasing approvals or manually tracking compliance status. Teams that run on Greenlight Guru are 3.5x less likely to receive a major audit finding. For R&D and product teams, it means staying in the tools they already use, with changes automatically syncing to design controls so documentation builds itself as you work, not after the fact as a separate project. Greenlight Guru AI handles the repetitive work that slows teams down, and it was built with 15 years of medtech context behind it, not bolted on from a general-purpose model. AI-powered search finds answers across your QMS instantly. Chat analyzes system data to surface insights. Auto-generated summaries give immediate context on documents, suppliers, and quality events. For product teams, verifiability checks catch vague requirements before they become audit findings, suggested links close traceability gaps automatically, and AI brainstorming gets engineers moving faster. For quality teams, AI generates training quizzes and drafts change order summaries, so your team spends less time writing and more time on the work that actually requires their expertise. The platform is validated out of the box and aligned to FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, EU MDR, and FDA 21 CFR Part 11. Implementation is measured in weeks, not the quarters-long projects that come with legacy enterprise platforms. Backed by 80+ audit-tested, customizable templates and a team of experts who know medtech inside and out. You're not managing a separate validation project before you can go live. For 15 years and across more than 1,000 device companies worldwide, Greenlight Guru has been the QMS medical device teams trust to pass audits, bring products to market, and stay on the market longer. [Visit website](https://www.g2.com/external_clickthroughs/record?secure%5Bad_program%5D=paid_promo&secure%5Bad_slot%5D=category_product_list_llm&secure%5Bcategory_id%5D=1194&secure%5Bchosen_at%5D=2026-07-31T16%3A44%3A43Z&secure%5Bmedium%5D=sponsored&secure%5Bprioritized%5D=false&secure%5Bproduct_id%5D=15578&secure%5Bresource_id%5D=1194&secure%5Bresource_type%5D=Category&secure%5Bsource_type%5D=category_page&secure%5Bsource_url%5D=https%3A%2F%2Fwww.g2.com%2Fcategories%2Fquality-management-qms%2Ffree%3Fpage%3D4&secure%5Btoken%5D=f204d1b2e1d45a016abc27350f9971b976498d8dd22b470d9d1dcecf67d42084&secure%5Burl%5D=https%3A%2F%2Fwww.greenlight.guru%2Fquality-management-software&secure%5Burl_type%5D=paid_promos) ### [QMex](https://www.g2.com/products/qmex/reviews) 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. #### Who Is the Company Behind QMex? - **Seller:** [BTS - Business Technology Solution](https://www.g2.com/sellers/bts-business-technology-solution) - **Year Founded:** 2012 - **HQ Location:** İstanbul/Türkiye - **Twitter:** @bts\_tr 292 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=caa75d42f1ef02fe211ee46368497f42958d9158fc3d77ef78540b141d992f09&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fbtstr&secure%5Burl_type%5D=linkedin_company_website) 30 employees on LinkedIn® - **Phone:** +90 216 566 00 50 ### [Q-Trust](https://www.g2.com/products/q-trust/reviews) 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. #### Who Is the Company Behind Q-Trust? - **Seller:** [Qredible, Inc.](https://www.g2.com/sellers/qredible-inc) - **Year Founded:** 2019 - **HQ Location:** Cherry Hill, US - **Twitter:** @GetInQredible 27 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=ce37a6ada75a2890c6fa5ce66b2113620501203bc8a5c2a7f03437c1bbf8af13&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fqredible-inc&secure%5Burl_type%5D=linkedin_company_website) 14 employees on LinkedIn® ### [QualiHQ](https://www.g2.com/products/qualihq/reviews) 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 #### Who Is the Company Behind QualiHQ? - **Seller:** [QualiHQ](https://www.g2.com/sellers/qualihq) - **HQ Location:** IE - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=383990414cbc93ef0901e555f62ffd3dabeae027551ef198077ab99dcc14ad62&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fqualihq%2F&secure%5Burl_type%5D=linkedin_company_website) 1 employees on LinkedIn® ### [QwizPRO](https://www.g2.com/products/qwizpro/reviews) 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. #### Who Is the Company Behind QwizPRO? - **Seller:** [Telonic IQ](https://www.g2.com/sellers/telonic-iq) - **HQ Location:** N/A - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=fb5c1cdd8cbbf0dd3b593ec113781d486d7dd20ddaf6ad824d599694c4a7d774&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftelonic-iq%2F&secure%5Burl_type%5D=linkedin_company_website) 1 employees on LinkedIn® ### [Siemens QMS Solution](https://www.g2.com/products/siemens-qms-solution/reviews) 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. #### Who Is the Company Behind Siemens QMS Solution? - **Seller:** [Siemens Digital Industries Software](https://www.g2.com/sellers/siemens-digital-industries-software) - **Year Founded:** 1980 - **HQ Location:** Plano, Texas - **Twitter:** @siemenssoftware 36,972 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=1dd3753f2277968b1f3c28e3070b9762650d5b5c8485137227b26fcbc85343e0&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F28423178%2F&secure%5Burl_type%5D=linkedin_company_website) 20,941 employees on LinkedIn® ### [SmartAPQP](https://www.g2.com/products/smartapqp/reviews) SmartAPQP connects APQP, FMEA, Control Plan, PPAP, RFQ, BOM/ECN, CAPA and supplier collaboration on one Part Master — built for IATF 16949 manufacturers. #### Who Is the Company Behind SmartAPQP? - **Seller:** [Smart Factory Solutions](https://www.g2.com/sellers/smart-factory-solutions) - **HQ Location:** N/A - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=7886df2ed926834e5eb248c77dcfa8e5c815d3ab1f0fe3132ced0dba45868834&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2FNo-Linkedin-Presence-Added-Intentionally-By-DataOps&secure%5Burl_type%5D=linkedin_company_website) 1 employees on LinkedIn® ### [TenForce](https://www.g2.com/products/tenforce/reviews) All in one EHSQ solution for Manufacturing, Pharmaceuticals, and Energy. TenForce unifies environmental, health, safety, quality, and compliance data in a single platform - ideal for plant managers and EHSQ teams across multi-site operations. Centralized Data Management: Find any document you need in seconds Streamlined Workflows: Automates tasks, notifications, and approvals, saving time and reducing errors. Improved Collaboration: Enables teams from different departments to stay aligned with shared dashboards and real-time updates. Simplified reporting: Customizable templates and scheduled reporting allows teams to automate recurring reports #### Who Is the Company Behind TenForce? - **Seller:** [TenForce](https://www.g2.com/sellers/tenforce) - **Year Founded:** 2001 - **HQ Location:** Louvain, BE - **Twitter:** @TenForce 279 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=ddc6447f90d44a04cdfd3abca15274c0b656665112fad825402c4b07ab64e32a&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Ftenforce%2F&secure%5Burl_type%5D=linkedin_company_website) 85 employees on LinkedIn® ### [TilliT](https://www.g2.com/products/tillit-tillit/reviews) The TilliT Digital Manufacturing Operations software enables fully paperless operations by integrating production, quality, and maintenance processes in a single low-code cloud platform. Light-weight and easily deployed TilliT combines asset performance monitoring, OEE, work order execution, quality management, knowledge management and production scheduling driven by workflow automation and AI optimization. By connecting to existing equipment or by using our suite of IoT sensors, TilliT brings together people, products, processes and equipment for complete operational control. **Average Rating:** 4.0/5.0 **Total Reviews:** 1 #### Who Is the Company Behind TilliT? - **Seller:** [TilliT](https://www.g2.com/sellers/tillit-05abfe48-8715-4f6b-9215-9346c3b64576) - **Year Founded:** 2021 - **HQ Location:** Brisbane City, AU - **Twitter:** @GoTilliT 11 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=56c0feeceda19b358c68f84bfd1a6cf4516aea19cbf6f835e856f21a343f3742&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fgotillit%2F&secure%5Burl_type%5D=linkedin_company_website) 8 employees on LinkedIn® #### Who Uses This Product? - **Company Size:** 100% Medium #### What Are Recent G2 Reviews of TilliT? **["Recommended"](https://www.g2.com/survey_responses/tillit-review-10573856)** **Rating:** 4.0/5.0 stars _— Andres Camilo S._ [Read full review](https://www.g2.com/survey_responses/tillit-review-10573856) ### [Wismatics](https://www.g2.com/products/wismatics/reviews) Wismatix QMS is a full-featured Quality and Compliance Management System that includes modules for: - Customer and Supplier Management - Customer and Supplier Complaints - Internal Defects and Deviations - Safety Issues - Quality Costs - Improvements - Unit/Service Management - Equipment Handling - Chemical Handling - RMA Management - Project Management (Agile/SCRUM) - Risk Management and SWOT handling - Product Management - Change Management - Analysis and Reporting - Process Management - Internal/External Audits - Management Evaluations - Documentation Management - Organization Management - Education and Training - Employee Roles, Responsibilities and Authorities Wismatix QMS contains all the features you need to run your Quality and Compliance Management System efficiently. The system supports - ISO 9001/9100, ISO 13485, FDA Title 21 CFR Part 820, - ISO 14001, ISO 45001, - ISO 27001, FDA Title 21 CFR Part 11, - and many more... #### Who Is the Company Behind Wismatics? - **Seller:** [Wismatics EOOD](https://www.g2.com/sellers/wismatics-eood) - **Year Founded:** 2022 - **HQ Location:** Popovo, BG - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=84fe988290b6b535b88d432e4aab8eca1d3cacd4c0c92a90d9db2a8062b531e4&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fwismatics&secure%5Burl_type%5D=linkedin_company_website) 2 employees on LinkedIn® ### [Xybion QMS](https://www.g2.com/products/xybion-qms/reviews) Rapidly Transform your Compliance, Quality & Risk Management Systems for Today’s All-Digital, All-Remote World :Predict, Mitigate, Automate and Monitor Compliance in Real-Time. Be Always Compliance Inspection Ready Xybion’s CQRM XD is a highly-adaptable and technologically-advanced Governance, Risk, Compliance (GRC) & Quality Management System (QMS) designed for today’s digital world. Purpose-built with embedded quality and compliance, this next generation enterprise risk management software platform ensures compliance, risk and quality in complex and highly-regulated industries. Xybion’s validated QMS software provides powerful cloud-based capabilities that facilitate organizational compliance with regulatory guidelines such as ISO 9001, ISO 13485, ISO 17025, ISO14001, GxP, 21 CFR Part 11, financial reporting and governance regulations (SOX, CA Bill 198), risk-based regulations and other industry standards. #### Who Is the Company Behind Xybion QMS? - **Seller:** [Xybion](https://www.g2.com/sellers/xybion) - **Year Founded:** 1977 - **HQ Location:** Princeton, New Jersey - **Twitter:** @Xybion 1,034 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=cbefe1bde37e841d20a42c36f8b0783f5c6791a54dcfb7d1c08b72d8ab913e4e&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fxybion-digital%2F&secure%5Burl_type%5D=linkedin_company_website) 240 employees on LinkedIn® - **Ownership:** TSXV: XYBN - [‹ Prev‹ Prev](/categories/quality-management-qms/free?order=g2_score&page=3#product-list) - [1](/categories/quality-management-qms/free?order=g2_score#product-list) - [2](/categories/quality-management-qms/free?order=g2_score&page=2#product-list) - [3](/categories/quality-management-qms/free?order=g2_score&page=3#product-list) - 4 - Next ›Next › Spotlight Categories [Zero Trust Networking Software](https://www.g2.com/categories/zero-trust-networking) [Customer Data Platforms (CDP)](https://www.g2.com/categories/customer-data-platform-cdp) [Attribution Software](https://www.g2.com/categories/attribution) [E-Signature Software](https://www.g2.com/categories/e-signature) [Accounts Payable Automation Software](https://www.g2.com/categories/ap-automation) Similar Categories - [Chemical Management](/categories/chemical-management) - [Environmental Health and Safety](/categories/environmental-health-and-safety) - [Ergonomics](/categories/ergonomics) - [Fatigue Risk Management](/categories/fatigue-risk-management) - [Inspection Management](/categories/inspection-management) - [Occupational Health and Safety (OHS)](/categories/occupational-health-and-safety-ohs) - [Permit to Work (PTW)](/categories/permit-to-work-ptw) - [Specification Management](/categories/specification-management) [Browse Quality Management (QMS) Themes](/categories/quality-management-qms/themes)