Alternatives to Quality Control Platform

Compare Quality Control Platform alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Quality Control Platform in 2026. Compare features, ratings, user reviews, pricing, and more from Quality Control Platform competitors and alternatives in order to make an informed decision for your business.

  • 1
    Epicor Connected Process Control
    Epicor Connected Process Control (CPC) is a flexible no-code/low-code MES and manufacturing operations platform that helps manufacturers improve quality, consistency, and visibility across production and assembly operations. Create digital work instructions with multimedia content, guide operators through critical tasks, connect equipment and devices across the shop floor, and capture production and quality data without extensive programming. CPC provides product traceability with a complete historical record of each product's build and inspection history. Real-time insights into quality, performance, defects, rework, and production trends help teams identify issues faster, reduce waste, and support continuous improvement. Manufacturers use CPC to standardize production and assembly processes, improve operator consistency, and support assembly verification, error proofing, quality inspections, and production monitoring across the shop floor. Whether deployed in a single work cell, across multiple production lines, or enterprise-wide, CPC scales to support manufacturers of all sizes. Available on-premises or in the cloud, it adapts to your operational requirements and manufacturing processes.
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  • 2
    Process Street

    Process Street

    Process Street

    Process Street is an AI-powered compliance operations platform that automates complex workflows, enforces standards, and tracks audit data in real time. Teams use it to create structured SOPs, assign tasks, collect data, and monitor execution with intelligent oversight. From onboarding and audits to vendor management and document control, Process Street ensures every step is followed and every action is logged. Built for regulated industries like financial services, healthcare, and manufacturing, it supports frameworks such as ISO, SOC 2, SOX, and HIPAA. With role-based permissions, audit logs, and powerful integrations, Process Street replaces static documents, spreadsheets, and manual processes with a single automated system of record. Use AI to streamline approvals, catch risks early, and generate audit-ready evidence. Trusted by teams at Cargill, DoorDash, Farmers Insurance, and Hartford Healthcare.
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  • 3
    Propel

    Propel

    Propel Software

    Propel is a cloud-native platform that unifies PLM, QMS, and PIM in one connected system, giving manufacturers complete visibility and control across the entire product lifecycle. It provides a single source of truth for product data, streamlines change management, strengthens quality and compliance, and accelerates time-to-market by eliminating silos. With real-world AI use cases and enterprise-grade security, Propel helps organizations reduce errors and improve cross-functional alignment. Agentic AI accelerates change reviews, surfaces BOM and quality risks, enriches product information, and guides decisions—while role-based permissions and audit trails protect IP. From design through manufacturing and commercialization, Propel empowers companies to deliver innovative, high-quality products faster with greater confidence. Each module deploys independently with no required dependencies.
    4.3 out of 5 stars 215 Ratings for Propel
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  • 4
    Epsilon3

    Epsilon3

    Epsilon3

    Epsilon3 is an AI-powered procedure and resource management tool designed for teams building, testing, and operating advanced products and systems. ✔ Standardize & Optimize Processes Our interoperable procedure execution system replaces inefficient checklists managed with paper, spreadsheets, docs, and outdated planning tools. Automatically track every step to ensure quality, consistency, and traceability. ✔ Fuel Rapid Iteration & Innovation Built-in version control, conditional workflows, and real-time data synchronization keep teams on the same page. Enable continuous improvement and quick, data-driven decisions to stay far ahead of the competition. ✔ Streamline & Scale Operations Securely integrate siloed systems and automate error-prone tasks to boost productivity and prevent delays. Simplify training, reduce costs, and maintain efficiency as your operations expand to meet demand. Trusted by industry leaders like NASA, Firefly Aerospace, and Commonwealth Fusion.
    4.2 out of 5 stars 265 Ratings for Epsilon3
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  • 5
    QBench

    QBench

    QBench

    QBench is a cloud-based Laboratory Information Management System (LIMS) designed to help laboratories manage samples, workflows, data, inventory, reporting, quality processes, and client interactions in one platform. Labs use QBench to manage laboratory operations from order placement and sample processing through results and automated reporting. The platform is highly configurable, allowing laboratories to build workflows, define custom data fields, and automate processes around the way their lab already operates. QBench also helps laboratories reduce manual work by connecting instruments, software, and other systems through file parsers and a robust API. These integrations can automate data transfer between systems, reducing repetitive data entry and the risk of transcription errors. Labs can connect QBench to business intelligence tools, including Tableau, Power BI, Domo, and Looker, via REST API. Key QBench capabilities include: Sample and workflow management Configurable laboratory workflows and custom data fields Workflow automation Instrument and system integrations File parsing and API connectivity Inventory management Client portal access Automated reporting Analytics and operational insights Business intelligence integrations with Tableau, Power BI, Domo, and Looker via REST API Integrated Quality Management System (QMS) capabilities Unlike LIMS platforms that require extensive custom development to accommodate laboratory processes, QBench is designed to be configurable and adaptable as workflows change. Laboratories can modify processes, fields, and automations without relying heavily on custom code. QBench is cloud-based, giving laboratory teams secure access to their LIMS while bringing laboratory data, workflows, automation, quality management, and reporting together within a centralized platform. QBench also supports customers with a team that includes former bench scientists who understand laboratory workflows and can provide guidance throughout implementation and ongoing use.
    4.6 out of 5 stars 153 Ratings for QBench
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  • 6
    QVscribe
    QVscribe, QRA's flagship product, unifies stakeholders by ensuring clear, concise artifacts. It automatically evaluates requirements, identifies risks, and guides engineers to address them. QVscribe simplifies artifact management by eliminating errors and verifying compliance with quality and industry standards. QVscribe Features: Glossary Integration: QVscribe now adds a fourth dimension by ensuring consistency across teams using different authoring tools. Term definitions appear alongside Quality Alerts, Warnings, and EARS Conformance checks within the project context. Customizable Configurations: Tailor QVscribe to meet specific verification needs for requirements, including business and system documents. This flexibility helps identify issues early before estimates or development progress. Integrated Guidance: QVscribe offers real-time recommendations during the editing process, helping authors effortlessly correct problem requirements and improve their quality.
  • 7
    Qualityze EQMS Suite
    Qualityze is a leading provider of cloud-based Quality Management System (QMS) and Enterprise Quality Management Software (EQMS) solutions built natively on the Salesforce platform. Designed to streamline quality processes, ensure regulatory compliance, and drive operational excellence, Qualityze empowers organizations to manage CAPA, audits, document control, training, change management, risk management, and supplier quality within a unified, scalable ecosystem. Focused exclusively on quality and compliance, Qualityze delivers purpose-built QMS and EQMS solutions without distractions from unrelated custom development. Our platform enables organizations across life sciences, manufacturing, and other regulated industries to simplify compliance with global standards while improving visibility, traceability, and accountability. Qualityze fosters a true culture of quality by making enterprise quality management intuitive, user-friendly, and collaborative.
  • 8
    MasterControl

    MasterControl

    MasterControl

    Bringing breakthrough products to market in highly regulated industries can feel like an endless series of trade-offs. MasterControl's software simplifies GxP workflows so you never have to sacrifice quality for cost or innovation for regulation. Complete and connected meets fast and flexible. From quality event management to document control and integrated training - MasterControl Quality Excellence transforms your quality data and processes into a competitive advantage. Modernizing your manufacturing operations starts with modern software. From work orders to work instructions and production records (EBR or eDHR) to logbooks, MasterControl Manufacturing Excellence is the simplest way to digitalize manufacturing.
  • 9
    digiQC

    digiQC

    Spaceify Technologies

    digiQC empowers your Site Engineers with a Construction Quality management software solution. With a quality management system in construction, you can take control, have increased visibility, and raise quality standards and accountability across your Quality Assurance team. Keep a check on your onsite projects without compromising on the quality. Get insights and catch alarming issues before the remedy exceeds your budget and project deadlines. Equipped with a mobile app as well as a web platform, empower your quality assurance team to record data digitally in real-time. Reduce the paperwork and human error involved in manual data filling. Create a workflow that ensures quality checks are filled at every step. Enable your site engineers to be accountable for the quality control, as well.digiQC Construction Quality Control app makes it possible for the site engineers to CAPTURE and RECORD real-time data onsite during the quality checks.
  • 10
    QUMAS EQMS

    QUMAS EQMS

    Dassault Systemes

    To bring new products to market as quickly as possible in compliance with global regulations, organizations need to standardize and automate their business processes that manage the collection, tracking and analysis of information and the resolution of related issues. QUMAS EQMS (formerly ProcessCompliance) is a cloud-based solution for Enterprise Quality and Process Management that delivers comprehensive integrated regulatory, quality and compliance management capabilities in a validated QMS environment. QUMAS’s data-centric approach allows you to flexibly manage quality content and to access and re-use all quality data, providing comprehensive visibility into Quality. QUMAS’s interactive quality dashboards provide QMS overview across business areas and quality initiatives. Reports are available for export, email and scheduling. QUMAS allows QMS departments to exchange information securely, efficiently and compliantly in the cloud.
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    LightTable

    LightTable

    LightTable

    LightTable is an AI-driven peer review platform for construction and real estate development documents that automates the identification of errors, omissions, coordination issues, and compliance gaps before construction begins. The system ingests architectural drawings, engineering specifications, and related PDFs, and within 10–45 minutes delivers a prioritized list of redlines and flagged issues across multiple disciplines, including constructability, MEP, accessibility, and fire & life safety. Its AI layers domain knowledge on top of computer vision and language models to interpret relationships between drawings and specifications, detect conflicts and gaps, and drive expert-in-the-loop validation workflows. LightTable claims to surface up to four times more issues than traditional peer reviews and reduce coordination mistakes by up to 70%.
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    AQF

    AQF

    BGR Informatique

    AQF is a management software of quality developed by professionals in quality control. AQF is a total solution that makes it possible to eliminate the procedures paper and it helps you to easily carry out all the stages of the actions in quality assurance. We offer a modular service to allow all companies to obtain a suitable product while avoiding unnecessary costs. Only the main module is mandatory for the installation of the additional modules. Our AQF module is not only complementary to its own modules. The AQF module is also complementary to the software and/or ERP already used by your organization. Create, manage and share your controls internally, your supplier's audits, your procedures, and your documents. Simplify procedures between users and assign specific rights to control outgoing information. Automate the request for documentation in order to avoid oversights. With the Internet of Things (IoT) connectivity, manage and control the temperature and humidity.
  • 13
    GlobalVision Text Inspection
    Make sure there are no unwanted changes as the text moves from the copy documents to the illustration files. Compare different documents to easily inspect all content and text attributes. GlobalVision's text inspection works by running a character-by-character comparison to inspect each Unicode value. It can detect up to 18 types of text errors, such as missing punctuation, font and color errors, inserted or deleted words, and more. Compare different file formats to automatically detect differences between master and sample documents. Generate comprehensive inspection reports to review and navigate through all the differences found. Compare hardcopy samples to digital files for fast and accurate inspections of printed packaging components. Compare text and spelling in over 30 foreign languages with dictionaries built directly into GlobalVision.
  • 14
    Docuply

    Docuply

    Docuply

    Docuply is a cloud-based electronic quality management system (eQMS) with integrated electronic document management and an electronic trial master file (eTMF) for clinical biotechnology companies, contract research organizations and other teams working in regulated drug development. It supports controlled document creation, review, approval, version tracking and electronic signatures, plus SOP training, deviation and corrective and preventive action (CAPA) workflows, supplier management, and trial-file organization using a CDISC TMF reference model. The platform provides audit trails, training records, document search and AI-assisted features for selected quality and document workflows. Teams can organize trial records and collaborate with external sites, sponsors and suppliers. Docuply is delivered as a web service hosted in the EU for GxP-related quality and clinical documentation processes.
  • 15
    Virje

    Virje

    Virje

    Virje complies with the requirements of 21 CFR Part 11, 21 CFR Part 820, and ISO 13485. Overwhelmed by the thought of Part 11 software validation? Accessible from wherever you are, for whenever you work. Eliminate paper, reduce cost, and increase efficiency with automation and centralized collaboration. Perfect for small to medium-sized businesses. Built from the ground up specifically for medical device quality management. A system that is flexible enough to adjust to your workflows and processes, without having to compromise. Configurable change order approvals by employee role and by document type. Notifications to responsible personnel at every stage in the change process. Ability to designate material dispositions for individual documents. Easy access to released and historical versions of documents. Quick viewing of document change history. Tracking of where-used locations and distributed hard copies. Periodic document review notification.
  • 16
    GMPPro

    GMPPro

    Motto Systems

    Quality is an ongoing process, a conscious practice to stay ahead in the business world. In core industries like pharmaceuticals, acceptability, approvals, and success ride on quality. Pharmaceutical is a highly regulated industry. Stringent regulations increase the complexity of managing business processes. In a continuous review and reinvention of activities and internal processes, deploying an integrative quality management system is crucial. In the context, GMPPro , a meticulous and robust quality management system from Motto Systems is the right deployment to resolve quality issues at any stage of drug development. A precision quality management solution, GMPPro is capable of encompassing the whole spectrum of production, quality control, quality assurance, and engineering in systemic integration and as independent solution modules as well. GMPPro is designed for total control of processes and backed by our industry-focused professional team.
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    DeepEyes

    DeepEyes

    DeepEyes

    The effective management of GMP-regulated manufacturing areas requires a holistic approach based on identifying and monitoring those components that play the most critical roles: facility, personnel and microbial control. By instantly recognizing compliance related anomalies and contamination threats, DeepEyes video-based AI error-recognition solutions close the gap that even the best training and supervision/monitoring leave open. The intelligent DeepEyes solutions automate surveillance by alerting deviations from good manufacturing processes (GMP) in real time; they provide constant quality control that goes parallel to the manufacturing process. Operator training cannot completely avoid the risk of leakage. Constant monitoring is required so as to prevent product loss, waste disposal issues, downtime as well as safety threats.
  • 18
    Arena QMS

    Arena QMS

    Arena, a PTC Business

    Arena’s product-centric quality management system (QMS) software enables medical device manufacturers to deliver safe and compliant products to market fast. Arena QMS streamlines new product development and introduction (NPDI) by connecting quality and product processes. Arena QMS ensures regulatory compliance to various quality standards and regulations, including FDA 21 CFR Part 820, Part 11 and ISO 13485. Arena QMS enhances visibility and traceability by controlling quality processes in context with bills of materials (BOMs), SOPs, DMRs, DHFs, specifications, drawings, and training plans.
  • 19
    QAD Redzone
    Redzone has taken the food, beverage, and CPG manufacturing markets by storm with a digital production system that was purpose built for lean manufacturing and continuous improvement. By empowering frontline workers as their productivity engine, customers regularly post and sustain 30+% productivity uplifts following their first 90-day deployment. Typical Outcomes: - Rapid double-digit productivity improvements - A collaborative workforce engagement system that reduces turnover - A culture of continuous improvement driven by your workers and sustained over the long term With specific modules for production, quality and maintenance all built on a social/mobile platform for everyone-to-everyone collaboration, you'll connect all levels of the business to catch concerns before they become issues and get them fixed!
  • 20
    QFacts

    QFacts

    QFacts

    QFacts is a cloud-based Quality Management System for pharmacies, compounding facilities, and regulated industries. It covers the full quality lifecycle: controlled document management with version control and approval workflows, training and competency tracking with curriculum-based assignments, event and complaint handling, root cause investigations, CAPA management, and change control. All with complete audit trails. Built for GAMP 5 and European GMP/GDP compliance, QFacts enforces role-based access control across organisations, sites, and departments. Quality managers configure review workflows, track due dates, and monitor compliance through real-time dashboards. Every action is logged and traceable, giving inspectors and auditors a clear chain of accountability from document approval through training completion to corrective action closure.
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    Litewave

    Litewave

    Litewave AI

    Litewave is an AI quality review platform for regulated manufacturers across pharma, biotech, CDMO, medical device, dietary supplement, food, cosmetics, and CPG sectors. It reviews batch records, device history records (DHRs), certificates of analysis (CoAs), and supplier documents against specifications, approved supplier lists, and required tests. Each flagged discrepancy links to its source page and field, helping quality teams review exceptions and sign off while keeping records audit-ready for FDA, NSF, SQF, and customer audits. Litewave handles paper and handwritten records as well as digitized workflows, and works with existing MES, QMS, LIMS, and ERP systems. Structured data supports quality and manufacturing analytics across batches, sites, and suppliers. Deployment options include on-premises and customer-cloud environments. Use cases include batch record and DHR review, supplier CoA verification, paper-to-digital batch records, audit readiness, and quality analytics.
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    DELMIAworks

    DELMIAworks

    Dassault Systemes

    Combine manufacturing, MES, supply chain, and ERP software to optimize your shop floor. Learn how DELMIAworks (formerly IQMS) can help increase visibility into every aspect of your manufacturing operation and solve your most trying production challenges. Prevent unnecessary downtime, while increasing manufacturing efficiency, quality, and profit margins. Improve decision making with real-time access to data across the entire supply chain. A single system for all ERP, manufacturing, MES, and supply chain requirements. Lower your overall cost of investment and maintenance by automating your business. Our easy-to-use solution can help you double plant output, eliminate human errors, and increase the efficiency of your production planning process. Manage, track and monitor the complete production process to eliminate unplanned downtime and increase throughput. OEE charts and graphs are dynamically updated with performance and quality data in real-time.
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    icmInspector

    icmInspector

    icMobile Systems

    icmInspector is a system for automation of control, review and audit processes. It consists of a central part responsible for administration and management and a mobile application for Android. Improvment of quality in the organization through the implementation of modern control, inspection and interial audit processes that allow for the detection of irregular and undesirable situations in an unreliable, dispersed way and in real time. Minimalization of operating costs by shortening the time of preparation and distribution of materials and tools for control activities by replacing them with electronic versions. Increase the efficiency of employees responsible for controls and audits thanks to tools of fast and flawless data collection, protecting against omission of key information and introducing the possibility of scheduling work. Eliminate errors, abuses and fraud in the control process, by enforcing only logically permissible responses, recording metadata of data collection.
  • 24
    Verint Quality Bot
    Manual quality management processes are costly and ineffective. Verint Quality Bot automates your quality program to save time and money, improve quality, and reduce compliance risk. Start today and see 5x ROI. Is your quality management program working? Screening a small percentage of calls may leave non-compliant interactions hidden, and risk fines, lost business or worse. Verint can help. Most contact centers only review between 1 and 3% of calls. This severely limits your ability to identify risks and manage quality and compliance. Verint Automated Quality Management can automate the whole quality management process and help you achieve better compliance. Evaluate calls, identify non-compliance and assign coaching—for 100% of voice and text interactions. In this way, you will quickly gain a new level of insight into your organization’s standards of service and compliance.
  • 25
    QEdge

    QEdge

    Sarjen Systems Pvt Ltd

    Sarjen’s Quality Management Software brings meaningful digital transformation to how quality is managed across regulated manufacturing environments. More than just a system to store compliance records, it uses AI to turn quality data into actionable insights. AI analyzes trends, spots early signals of deviation, and predicts potential quality risks before they impact products or processes. Automated alerts and intelligent recommendations help teams act faster, reduce manual errors, and strengthen decision-making with context-aware guidance. With machine learning, the system continuously learns from data patterns and improves accuracy over time. By combining robust quality workflows with AI-driven intelligence, the solution enhances product consistency, accelerates investigation cycles, and ensures stronger compliance. It makes quality management smarter, more proactive, and easier for your teams to adopt and trust.
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    Trace One

    Trace One

    Trace One

    Gain a comprehensive, 360° view of product and packaging development for private label launches in the CPG retail sector. Trace One PLM is an integrated platform and single source of truth that provides end-to-end traceability and visibility across the entire product lifecycle—accelerating your private label go-to-market strategy on a global scale. With predefined templates, automated lifecycle processes, and a centralized, collaborative platform, Trace One PLM speeds up product development and launch while ensuring consistency and compliance. Empower seamless, real-time collaboration among all stakeholders—from innovation and R&D to regulatory, suppliers, quality, and packaging teams.
  • 27
    Nova-QMS

    Nova-QMS

    Novatek International

    Maintaining consistent product quality and quality processes can be challenging in today’s pharmaceutical manufacturing environments. Regulated industries such as the Pharmaceutical, Biotech and Life Sciences are required to maintain Good Manufacturing Practices (GMP) to meet regulatory requirements. Not only do you need to meet GMP requirements you must also be able to prove this. Using paper-based forms, disconnected systems, or manual processes to manage, track and report on quality issues and actions does not provide effective solutions for implementing harmonized, integrated quality management processes, which follow industry best practices.
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    Veeva Vault QMS

    Veeva Vault QMS

    Veeva Industries

    Ensure quality and GxP compliance with Vault QMS. With built-in best practices and automated workflows, Vault QMS brings all parties – pharma and biotech companies, contract manufacturers, and suppliers – into quality processes for better control and visibility. Easily bring departments, sites, suppliers, contract manufacturers, contract test labs, and other partners into continuous quality improvement processes. Increase operational efficiency with automated workflows and built-in best practices. Improve risk visibility across products and processes with a unified approach to risk management. Improve speed, efficiency, and GxP compliance with a unified suite of quality applications. Readily enable quality management processes with built-in best practices for deviation, internal and external audits, complaints, lab investigations, change control, CAPA, and quality risk management.
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    AcceleratorKMS (Procedure Accelerator)

    AcceleratorKMS (Procedure Accelerator)

    Innovatia Accelerator Inc.

    With AcceleratorKMS organizations can eliminate information-caused incidents. Equip workers with mobile-ready content. Review and evergreen information. Streamline authoring and save costs. Monitor work and find efficiencies. Decrease time and money spent during onboarding. The Accelerator provides an integrated digital content ecosystem in an easy-to-use and intuitive package focused on making the complex simple. Our goal is to make information easier to find for front-line workers, making operations safer. Reduce the chance of human error by giving workers instant access to digital Standard Operating Procedures (SOP), policies, and training content on a mobile device. Reduce the chance of information-caused incidents through standardizing all operational content, and make it easier to use with AI-assisted procedure authoring. Reduce administrative involvement and management effort as standardization reduces the overall amount of operational content.
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    AssurX

    AssurX

    AssurX

    The AssurX platform is a versatile enterprise quality management system (EQMS) and regulatory compliance management platform. AssurX allows enterprises of any size or complexity to create a system that reliably communicates and coordinates quality and compliance information, documentation, and activities across the enterprise. AssurX allows regulated businesses to quickly identify and control risk exposure and avoid quality or noncompliance problems while improving workflow. AssurX QMS software is highly configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. Begin with just the solutions and functionality you need now, then implement what you like whenever you’re ready. No other system is easier to deploy, configure, and modify.
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    FARO

    FARO

    FARO Technologies UK

    We are an imaging company — and an imagining company. We imagine a better, more insightful and capable world realized through 3D digital means and measurement technologies. From the beginning, we’ve been helping our customers make better decisions more quickly and accurately than anyone in the industry. The errors and non-conformance issues you don’t catch cause unnecessary waste, rework and unhappy customers. When delays matter, the right inspection technologies help. Struggles with alignment and part placement slow down production processes. When speed counts, precision measurement tools are the solution. The most innovative designs lose their wow factor if the products can’t be manufactured. When you need to stay ahead of the competition, 3D modeling solutions give you the edge. A bearings manufacturer purchased a Gage FaroArm to speed up inspection time without sacrificing measurement accuracy.
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    Seerene

    Seerene

    Seerene

    Seerene’s Digital Engineering Platform is a software analytics and process mining technology that analyzes and visualizes the software development processes in your company. It reveals weaknesses and turns your organization into a well-oiled machine, delivering software efficiently, cost-effectively, quickly, and with the highest quality. Seerene provides decision-makers with the information needed to actively drive their organization towards 360° software excellence. Reveal code that frequently contains defects and kills developer productivity.​ Reveal lighthouse teams and transfer their best-practice processes across the entire workforce.​ Reveal defect risks in release candidates with a holistic X-ray of code, development hotspots and tests. Reveal features with a mismatch between invested developer time und created user value.​ Reveal code that is never executed by end-users and produces unnecessary maintenance costs.​
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    Metaware QMS Platform
    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. Metaware reduces administrative burden, increases transparency and supports continuous improvement, making it suitable for both SMEs and enterprise-level organizations focused on professional quality assurance and compliance management.
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    WoodWing Scienta
    WoodWing Scienta is a cloud-based quality management system (QMS) for managing processes, policies, procedures, documents, risks, audits, forms and organizational knowledge in one controlled environment. Quality, QHSE and compliance teams can manage version control, approvals, review cycles, responsibilities, audit trails and improvement actions. Employees can find current information, complete tasks and forms, confirm reading assignments and submit change proposals. Scienta AI Search answers questions using approved content from the organization’s own environment while respecting access rights and showing source information. Dashboards, process flowcharts, structured registers, public forms and Microsoft SharePoint integration support quality management across teams and locations. Ready-to-use handbook content for ISO 9001, ISO 27001, healthcare quality and AI governance helps organizations build or improve a management system without starting from scratch.
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    Auditrunner

    Auditrunner

    Auditrunner

    The Secure Audit, Risk, Compliance & Quality Software. With On-Premise and Cloud-based deployment options. Auditrunner offers granular encryption and role-based access control for audit files and documents at-rest. All data transfers are protected. We have automated 3000+ business processes for enterprises around the world. Our GRC platform modules are just a few of them. Cloud-based or On-Premise, deploy and start using. Hassle-free integration process enables you to enjoy the benefits of the platform within weeks of kickoff . The low-code platform we are built upon is fully customizable and allows for compliance with any standard or regulation. Operate in a responsive manner in today’s fast-moving, ever-changing regulatory environment and comply with multitude of different legislation instantly without the need for assistance. The ease of use we offer is unmatched.
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    Reva QMS

    Reva QMS

    Reva Solutions

    Reva QMS is a software-based Quality Management System. Our solution is designed to help organizations collect, organize, manage, and report on their business-critical documents while aligning their business processes to comply with relevant industry standards, specifications, laws, and regulations. Specifically designed for highly regulated industries, Reva QMS helps organizations automate and streamline their paper processes for increased efficiency and regulatory compliance. It provides a comprehensive set of out-of-the-box functions and capabilities specifically designed for highly regulated industries to help them achieve greater operational transparency and comply with rules and regulations, policies, best practices, and industry standards. It provides an easy-to-use browser interface that allows users to manage critical business processes easily and in a simple manner.
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    EasyQA

    EasyQA

    ThinkMobiles

    In order to start catch crashes which can appear in you Android or iOS applications, you need to integrate EasyQA Software Development Kit with the code of your apps. To download SDK and find full instructions on connecting it to a project, you can open the Integrations page within your project in EasyQA Test Management Tool. When you connect the SDK to your project, use the generated token and initialize it in the application class of your project. After that you can create your app’s build and upload it in Test Objects within your project in EasyQA and your application starts to send crashes to the service. After you have added our EasyQA SDK into your project and uploaded it to Test Objects within your project in EasyQA, you can track your app’s crashes on our website. You just need to download the app to any Android or iOS device and start testing. When there is a crash, reboot the app and press Upload button.
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    Unifize

    Unifize

    Unifize

    Speed up innovation and continuous improvement by 3x in 30 days. Unifize is a software platform that makes innovation, quality, and CI processes collaborative. This helps manufacturing companies bring better products to life, faster. Whether you start with a single solution or deploy Unifize across all functions, you can be sure it works well in your environment. The templates are infinitely customizable and eliminate silos by connecting your processes together. Unifize is the only PLM tool that focuses on bringing teams together in a real-time collaborative environment to solve problems and manage critical innovation processes. If you're looking to upgrade to a complete quality suite, look no further. Unifize is the only eQMS that makes every quality process collaborative and easy to follow. Stop paying lip service to your APQP/PPAP processes. Bring teams together in a dedicated real-time conversation for every record.
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    qmsWrapper

    qmsWrapper

    qmsWrapper

    qmsWrapper is a connected Quality Management System (eQMS) built specifically for medical device startups and SMEs. Instead of implementing a complex enterprise platform from day one, organizations can grow their QMS through three connected editions: Foundation, Lifecycle, and Vigilance. Foundation helps companies move from paper forms, Word documents, and spreadsheets to controlled documents, workflows, training, and AI-assisted quality processes. Lifecycle adds CAPA, Quality Events, Change Control, Risk Management, Technical File management, Supplier Quality, and Smart Traceability Matrix. Vigilance extends the platform with post-market surveillance, regulatory oversight, audit readiness, and AI governance. Built for ISO 13485, ISO 14971, FDA QMSR, FDA 21 CFR Part 11, and EU MDR, qmsWrapper helps companies scale their quality system without rebuilding or migrating to another platform.
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    Genebra

    Genebra

    Genebra

    Create and manage documents online, preventing misplaced printed copies and lack of organization. Gather all information in one place and make it easy to monitor and address nonconformities. Define, collect, and analyze KPIs through comparative charts, to help you with decision making. Plan and implement actions to address risks and opportunities in a simple and controlled way. Overcome spreadsheets and printed copies. Get file control in a cloud base with 24/7 access from any location and device. Optimize document elaboration, review, and approval. Manage access permissions and automatic notifications about document changes and expiration dates. Have always the most recent versions of all files uploaded into Genebra. Do not waste time browsing through numerous spreadsheets, and never lose revisions of your documents.
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    TelStrat QM

    TelStrat QM

    Serenova

    Empower your supervisors, trainers, Quality Assurance teams, and agents to optimize customer interactions. Review live-monitored and recorded calls, and synchronized voice and screen recordings via a user-friendly interface. Automatically analyze interactions for actionable insights. Enhance service quality, determine call-handling effectiveness and confirm agents are adhering to scripts and processes, all with a sophisticated call center quality management software. Easily manage team performance via intuitive interface. Listen, watch, evaluate and score agents, and deliver effective coaching and e-Learning. Provide packaged call content with e-Learning resources to coach agents and improve KPIs with instant, relevant, and regular feedback. Easily, efficiently and quickly perform evaluations. Prepare agents to excel by providingin-depth performance reporting.
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    Quality Forward

    Quality Forward

    Quality Forward

    Quality Forward is a cloud-based electronic Quality Management System (eQMS) designed to help organizations in highly regulated industries digitize, manage, and automate their quality processes within a unified platform. Built on the ServiceNow architecture, it enables teams to centralize and control critical workflows such as deviations, corrective and preventive actions (CAPAs), audits, complaints, change control, document management, training, supplier quality, and risk management, all with full traceability and audit-ready documentation. It provides real-time monitoring, automated workflows, and AI-driven insights that streamline compliance, reduce manual effort, and improve operational efficiency across the product lifecycle. It offers a highly configurable, no-code environment that allows quality assurance teams to adapt processes to evolving regulatory requirements without relying on IT, while maintaining adherence to global standards such as FDA, ISO, and GxP.
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    ISNetworld

    ISNetworld

    ISN Software

    ISN is the global leader in contractor and supplier information management. ISN’s platform, ISNetworld®, serves as a world-class forum for sharing industry best practices, benchmarking performance and providing data insights among its members. Hiring Clients use ISNetworld to streamline their contractor and supplier qualification processes and drive improvement in their supply chains. ISN collects and reviews company health, safety, ESG, insurance, financial and training information, streamlining the qualification process and strengthening relationships with multiple Hiring Clients. Contractors and suppliers submit information into ISNetworld based on regulatory and Hiring Client requirements. ISN's Review and Verification Services (RAVS™) Team reviews self-reported information and documentation and conducts interviews with contractor personnel to assess the implementation of policies and programs.
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    Fast Quality Software

    Fast Quality Software

    Fast Quality Software

    Fast Quality Software is a comprehensive quality management solution designed to streamline quality assurance processes across various industries. Fast Quality Software facilitates the management of quality-based processes such as non-conformance and corrective actions, improves data integrity and consistency, enforces controlled and repeatable processes, and provides audit information and reporting. It aids in measuring the cost of quality/non-conformance, communicating quality across the enterprise, capturing necessary quality data for compliance, identifying improvement opportunities, and managing changes. By implementing Fast TQM Software, organizations can improve product quality, lower production costs, enhance decision-making, maintain traceability and compliance, monitor supply chains, decrease human error, minimize waste, reduce inventory costs, and optimize manufacturing process efficiency.
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    Nova-Stability

    Nova-Stability

    Novatek International

    Managing a stability study is a complex process and mistakes can occur. Using a manual paper based system increases the risk of errors. The only solution is to implement a software based process that automates your stability studies and shelf-life analysis. Stability studies are highly scrutinized by regulatory agencies. Companies must be able to prove the validity of their data. Automated solutions provide the ability to produce the necessary documentation in real-time to satisfy auditors. Systems like Nova-Stability helps companies maintain regulatory compliance while reducing risk to the patient. Nova-Stability is a powerful process based feature-rich system that manages the entire stability testing process. This comprehensive solution is compliant with current regulatory guidelines on a global level. Nova- Stability accommodates all types of stability studies.
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    TIPQA

    TIPQA

    Deltek

    Companies use TIPQA to achieve continuous and measurable improvements while advancing customer service, productivity and profitability. Our QMS software allows industry leaders to control compliance and effectively manage quality within their supply chain. TIPQA QMS Software supports best practices in quality and will help you build a comprehensive continuous improvement strategy for your organization. Use of the TIPQA quality management solution has resulted in proven, documented success by countless companies that demand delivery of highly regulated, quality products. TIP Technologies has more expertise in understanding complex quality business processes in a regulated manufacturing environment than any other solution pro­vider. The TIPQA quality management solution allows its users to remain agile, allowing them to adapt to ever-changing markets and quality requirements. TIP Technologies continuously develops its quality management system.
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    BriefCatch

    BriefCatch

    BriefCatch

    Reduce the time and energy spent editing others' writing by leveraging BriefCatch's powerful legal-specific editing tools. With BriefCatch, swiftly identify and correct embarrassing typos and errors to ensure your writing remains impactful and flawless. No matter who you are, BriefCatch supports your drive to be the best with draft scoring, advice, and tips to improve your writing. Tailored legal writing suggestions and guidance with one-click, trackable changes. Analyze and score your work with actionable feedback for targeted improvements. Analyze your writing style, pinpointing strengths and weaknesses for long-term improvement.
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    Otter Systems

    Otter Systems

    Otter Systems

    Compliance Management Software for the Cannabis Industry. Optimized Cannabis Compliance Software. ​The medical cannabis industry is highly regulated. Most states require cultivators, processors, and distributors to keep track of every seed, ounce of flower, and edible they sell or discard for quality issues. To stay on the right side of the law in the cannabis market, you need to have a paper trail for all transactions from the cultivation to the final sale. ​Constant shifts in an ever-evolving medical marijuana marketplace, coupled with the need to ensure compliance and reduce risk can no longer be managed with traditional software or manual templates alone. Features You Need to Succeed. ​Otter Systems Compliance Management Software provides a centralized platform for tracking regulatory requirements, organizing compliance documentation, and managing compliance processes, with features including: Cannabis Document Control, Policy Management, Change Management, Supply Chain Control.
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    ConforgeLabs

    ConforgeLabs

    ConforgeLabs

    ConforgeLabs™, part of ThoughtMinds, builds agentic AI networks for manufacturing OEMs, integrating directly with existing ERP systems with zero migration. Its Engineering Drawing Validator catches GD&T errors and revision conflicts in drawings and BOMs before production. Quote AI converts CAD data and quoting history into fast, accurate cost estimates, cutting RFQ turnaround time. Smart Troubleshooting is an AI field-service assistant that uses manuals and fault-code history to speed up repairs. Warranty Intelligence deploys 25+ specialist AI agents and computer vision to detect fraudulent or tampered warranty claims. Supplier Intelligence flags supplier risk and disruption patterns in real time, helping manufacturers avoid production delays before they happen.At ConforgeLabs, every recommendation our agents generate is traceable, explainable, and backed by an auditable decision trail, so your teams stay in control while AI does the heavy lifting.
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    EPIQ QMS by Caliber

    EPIQ QMS by Caliber

    Caliber Technologies

    Caliber’s Integrated Quality Management platform – EPIQ stands out from the crowd of generic quality offerings in the market. Caliber offers unmatched, in-depth integrations and functionalities across departments making it far more capable of providing a seamless quality management experience like no other. In addition, this platform offers capabilities that go beyond regular quality management requirements and provides a foundation for quality metrics, performance analytics, CPV, and PQR. Many companies are heavily investing into automation currently. Yet, there still are inadequacies in terms of information sharing across departments. Quality Assurance departments are mandated to see the effect of a deviation across the other departments. Many planned and unplanned changes have to go through more than one department for analysis and closure. As part of risk mitigation, interdepartmental transactions gather high importance.