Top Free Quality Management Systems (QMS) - Page 2

How Many Quality Management Systems (QMS) Products Does G2 Track?

Total Products under this Category: 410

Category Stats (Oct 2026)

  • Average Rating: 4.42/5 (↑0.01 vs Sep 2026) The average rating of products in this category, based on all submitted ratings
  • Top Trending Product: Aptean Process Manufacturing OEE (+5.33%) - Among all products in this category, Aptean Process Manufacturing OEE recorded the largest rating increase compared to last month

Last updated: October 15, 2026

How Does G2 Rank Quality Management Systems (QMS) Products?

Why You Can Trust G2's Software Rankings:

  • 30 Analysts and Data Experts
  • 9,900+ Authentic Reviews
  • 410+ 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

Highlighted products: MasterControl Quality Management System, Redzone, Qualio, EASE, Octave Reliance (ETQ Reliance), QT9 QMS, Ideagen Quality Management, 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=qad-redzone&focus%5B%5D=qualio&focus%5B%5D=ease-inc-ease&focus%5B%5D=octave-reliance-etq-reliance&focus%5B%5D=qt9-qms&focus%5B%5D=ideagen-quality-management&focus%5B%5D=sap-cloud-erp-sap-s-4hana-cloud)

flowdit

flowdit is a no-code platform for inspections, audits, digital checklists and work instructions in industry and manufacturing. It is a connected worker solution for the people who run production lines, manage quality on the shop floor and keep equipment running. The problem with most inspection tools Most tools record the failure and stop there. The finding ends up in a PDF, someone eventually emails the maintenance team, and the line keeps running with the problem unfixed. flowdit closes that gap. When a check fails, the inspector assigns a corrective action with an owner and a due date on the spot. For critical points, this can be made mandatory. flowdit sends reminders until the action is closed, and it stays linked to the inspection step with a full audit trail. What manufacturing teams deal with Paper checklists disappear. Excel sheets end up in five versions. Audit preparation takes weeks because documentation is scattered across folders, inboxes and clipboards, and quality managers cannot see what is happening at other sites. flowdit brings all of it into one system. How it works Templates are built without code. The AI import turns existing Excel, Word or PDF checklists into templates, and for paper lists a photo is enough. Measurement fields with tolerances and mandatory fields keep inspections complete, while conditional questions keep them short. Templates are versioned and only go live after approval. In the field, inspectors download an assignment once and then work offline. They record measurements with photos or video, dictate notes by voice and sign off on the device. Results sync as soon as they are back online. Work instructions with images or video open right at the inspection step. Suppliers and external technicians complete checklists through a secure portal. Who uses flowdit Plant managers who need to see what is happening across sites without compiling reports on Friday afternoon. Quality managers preparing for ISO audits. EHS managers who need safety procedures to reach the person doing the job. Maintenance teams running inspection rounds. Commissioning engineers documenting FAT and SAT. Frontline operators who need a tool they can pick up quickly. Where it is used Quality inspections, internal and external audits, safety walks and EHS inspections, maintenance rounds, shift handovers, machine acceptance and commissioning. Customers come from automotive, mechanical and plant engineering, food and beverage, pharmaceuticals, chemicals and energy. Integrations and deployment A REST API connects flowdit to SAP and other ERP systems. Further integrations include DocuSign, DocuWare, Azure, Google Workspace, Zapier and Dropbox. All data can be exported at any time. Data is encrypted, flowdit is GDPR compliant, and it runs in the cloud or on-premise from 50 users. The app is available in 12 languages, and support is provided in English, German and Arabic. Pricing Free plan for a single user. Standard costs €12 and Premium €22 per user per month, both from 5 users. Enterprise pricing on request. Company flowdit is developed by iotivata FZCO, with offices in Germany and Dubai.

Average Rating: 4.9/5.0

Total Reviews: 30

How Do G2 Users Rate flowdit?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)

Who Is the Company Behind flowdit?

  • Seller: IOTIVATA - FZCO
  • Year Founded: 2018
  • HQ Location: Dubai, AE
  • Twitter: @flowdit_com
    2 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    10 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Manufacturing, Information Technology and Services
  • Company Size: 63% Medium, 37% Small

What Do G2 Reviewers Say About flowdit?

AI-generated summary from verified user reviews

Pros
  • Users love the user-friendly interface of flowdit, making training and collaboration effortless and efficient.
  • Users praise efficiency in flowdit, enabling smooth workflows and swift training for field teams with minimal paperwork.
  • Users highly value the real-time data capability of Flowdit, enhancing collaboration and decision-making on-site.
  • Users value the audit efficiency of flowdit, facilitating seamless inspection processes and improved compliance tracking.
  • Users value the automation of workflows in flowdit, enhancing efficiency and minimizing paperwork in inspections and audits.
Cons
  • Users feel that Flowdit requires improvement in customization visibility and performance during large file syncing for a better experience.
  • Users find the learning curve challenging, especially non-technical users needing help with initial setup and complex features.
  • Users find the initial setup of complex workflows requires guidance, which can complicate the onboarding experience.
  • Users note data inaccuracy issues, indicating a need for improved syncing and advanced visualization features.
  • Users find the difficult learning process challenging, especially non-technical users adapting to all features.

What Are Recent G2 Reviews of flowdit?

ACE

ACE is a cloud-based electronic quality management system built for regulated life sciences organizations. It brings quality processes, documents, training, and compliance activities together in one connected platform, helping teams maintain control, improve visibility, and stay prepared for audits and inspections. ACE supports core quality processes including document control, training management, deviations, CAPA, change control, risk management, audits, inspections, supplier quality, complaints, and more. Configurable workflows allow organizations to align the system with their existing processes while maintaining clear ownership, approvals, audit trails, and reporting. Designed specifically for regulated environments, ACE provides pre-validated starting points, electronic signatures, role-based access, version control, and complete traceability across quality records. Built-in dashboards and analytics give teams greater visibility into overdue actions, recurring issues, training status, and quality trends. ACE can support organizations at different stages of growth, from companies moving away from paper and spreadsheets to global teams replacing an existing eQMS. Its modular structure allows organizations to start with the capabilities they need and expand over time. Backed by PSC Software’s life sciences and compliance experience, ACE is developed in close collaboration with customers. The platform is designed to support practical quality management, reduce administrative work, and help regulated teams maintain an inspection-ready state.

Average Rating: 4.7/5.0

Total Reviews: 31

How Do G2 Users Rate ACE?

  • Has the product been a good partner in doing business?: 9.3/10 (Category avg: 9.1/10)
  • Corrective Actions: 9.6/10 (Category avg: 8.8/10)
  • Conformance Records: 9.6/10 (Category avg: 8.9/10)
  • Flexibility: 9.6/10 (Category avg: 8.6/10)

Who Is the Company Behind ACE?

  • Seller: PSC Software
  • Year Founded: 2009
  • HQ Location: Pomona, CA
  • LinkedIn® Page: www.linkedin.com
    23 employees on LinkedIn®
  • Phone: 1-828-237-8767

Who Uses This Product?

  • Top Industries: Pharmaceuticals, Biotechnology
  • Company Size: 63% Medium, 37% Small

What Do G2 Reviewers Say About ACE?

AI-generated summary from verified user reviews

Pros
  • Users enjoy ACE's exceptional tools for productivity and personal growth, making learning and workflow management seamless.
  • Users value the excellent customer support of ACE, which aids in overcoming the initial learning curve effortlessly.
  • Users value the user-friendly interface of ACE, which simplifies workflows and supports continuous learning effectively.
  • Users find ACE's easy learning curve beneficial, aided by helpful tutorials and strong community support for productivity.
  • Users love the efficiency of ACE, which seamlessly boosts productivity and supports continuous learning.

What Are Recent G2 Reviews of ACE?

Scilife

Scilife is a validated electronic Quality Management System (eQMS) purpose-built for life sciences organizations, including Pharma, Biotech, and Medical Device companies. Scilife consolidates the entire quality management lifecycle into a single, compliant platform—covering document control, training management, deviations, CAPAs, change control, audits, supplier and risk management—so quality teams can work efficiently while remaining continuously audit-ready. Designed for GxP-regulated environments, Scilife enables quality-driven organizations to automate quality processes, reduce manual and repetitive tasks, and gain real-time visibility into what’s open, overdue, and at risk across workflows. The result: fewer surprises during inspections and more time focused on meaningful quality improvement. ＋ What teams achieve with Scilife: • Reduce operational overhead while strengthening quality governance • Standardize quality workflows across products, sites, and global teams • Maintain complete, traceable audit trails for inspections and internal audits • Prepare smoother regulatory submissions with structured, reliable quality data Customers report up to 50% lower quality assurance costs and up to 30% faster time-to-market after adopting Scilife. ＋ Built for compliance, without the burden. Unlike general-purpose QMS or document management tools, Scilife provides a validated, GAMP 5-aligned eQMS software out of the box, significantly reducing validation effort and long-term maintenance. Automatic updates, built-in validation tools, and controlled releases allow teams to stay compliant with evolving regulations without heavy documentation or revalidation cycles. Organizations typically deploy Scilife faster than legacy eQMS solutions, while maintaining the level of rigor expected by regulators and notified bodies. ＋ Scalable, flexible, and ready to grow with you. Scilife’s flexible licensing model and product scalability allow teams to start with what they need today and expand as operations grow—without disrupting compliance or efficiency. Tiered pricing and rapid onboarding make it easy to adopt Scilife at any stage, from early-stage companies to global, multi-site organizations. ＋ Trusted by regulated teams worldwide Scilife is trusted by hundreds of life sciences companies worldwide. The platform supports compliance with FDA 21 CFR Part 11, ISO 13485, EU MDR, MDSAP, GxP, and ICH Q10 requirements. Behind the software is a dedicated customer success team who understand the realities of regulated environments and support teams well beyond onboarding. ＋ Predictable quality—scaled across teams. Scilife helps life sciences teams move from reactive quality management to proactive, data-driven, and continuously improving quality systems. Ready to build a brighter, more resilient quality foundation?

Average Rating: 4.3/5.0

Total Reviews: 76

How Do G2 Users Rate Scilife?

  • Has the product been a good partner in doing business?: 9.1/10 (Category avg: 9.1/10)
  • Corrective Actions: 6.7/10 (Category avg: 8.8/10)

Who Is the Company Behind Scilife?

  • Seller: Scilife N.V.
  • Company Website:
  • Year Founded: 2017
  • HQ Location: Antwerp, BE
  • Twitter: @ScilifePlatform
    956 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    122 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Pharmaceuticals, Medical Devices
  • Company Size: 61% Medium, 36% Small

What Do G2 Reviewers Say About Scilife?

AI-generated summary from verified user reviews

Pros
  • Users appreciate the ease of use of Scilife, benefiting from its user-friendly interface and varied modules.
  • Users appreciate the user-friendly modular design of Scilife, enhancing internal adoption and usability.
Cons
  • Users face serious module issues that raise concerns over validation, data integrity, and timely support resolution.
  • Users report poor customer support from Scilife, experiencing unresolved issues and inadequate communication over lengthy periods.
  • Users report major software bugs in SciLife, raising concerns about validation and data integrity, with inadequate support responses.

What Are Recent G2 Reviews of Scilife?

What Are G2 Users Discussing About Scilife?

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AuditRunner

✅ Auditrunner is designed to provide a user and budget-friendly, comprehensive low-code software platform that encompasses all facets of Internal Audit, Risk, Compliance (GRC), and Quality Management. ✅ The architecture allows organizations of all sizes to interconnect people and systems to design and run GRC processes seamlessly. SOX, Internal Audit and Audit Analytics can all be managed on one platform. Previous Audits, Risk Scores and many other details can be copied from previous years. ✅ It offers a document management module, which lets administrators create and distribute regulatory compliance documentation among internal teams and maintain an automated audit trail to track revisions or performed tasks. ✅ With Query Analyzer, data sampling, 100% population testing, continuous monitoring, linking data with findings and direct communication with business units is possible. We make it simple for the audit team. There is no need for an admin to manage the Query Analyzer or the permissions on AuditRunner. ✅ Integrate with 3rd Party software through open API for real-time data feed. Enter your own scripts or ask us to develop them for you and execute endless number of searches on the same data set to automate controls testing. Put findings in custom reports and export directly to Excel or PowerBI. ✅ AuditRunner is designed with COSO Framework in mind and is ready for SOX, risk and process based auditing. Keep a catalog of risks and controls in the form of a Risk and Control Matrix, keep Impact and Likelihood criteria scores, rate inherent and residual risk, create Heat Maps and follow up of Management Action Plans all on one platform. The technology we are built upon digitalized 4000+ business processes for 10+ industries in 15 years. The modules Auditrunner offers are just a few of these processes. Think of the possibilities within individual organizations. AuditRunner is awarded High Performer Badges in Audit, Operational Risk and Quality Management on G2. Auditrunner helps Financial institutions with interactive base and dynamic CRA/BRA calculations and reports. Security Operations Compliance (SOC) Report available for review of Clients. Auditrunner is used by companies from across various industries such as: • banking, insurance • financial services • energy • biotechnology • FMCG • manufacturing • non-profit • retail Why AuditRunner Top10: ✳️Make it your own. Low-cost, quick (within days) customization options according to your own company flows and approval schemes. ✳️Let us draft it. Automatically draft your audit report, executive summary or any other report with your templates. Edit and complete in less time. ✳️Seeing is believing. Abundant dashboard and graphic options with the possibility to add more or export to other BI tools for further reporting. ✳️Time is money. Quick onboarding (as quick as a week), short time from contract-to-market, with quick integrations with your internal systems. ✳️You have options. Manage your IT Dependency by writing your own SQL codes to dig into data or ask us to write them for you. ✳️Continuous Monitoring is key. Automatically flag items, send them for management response and embed results into your audit flow. ✳️Everyone in. Invite users easily with flexible user bucket pricing without them having to log-in and out to match the licensed user number. ✳️You’ve got this. Simple parameter setting and user management without the need to consult IT department or employ a tech person. ✳️Should not cost a fortune. Pay monthly or yearly, as you need with minimal upfront fees, free trainings and dashboards and report templates. ✳️Access it anywhere. This decade’s tech allows you to access the platform on any device, even your phone without the loss of functionality. Respond Use a tool that will make it possible to operate in a responsive manner in today‘s fast-moving, ever-changing regulatory environment that presents the challenge to comply with a multitude of different legislation. Design your own platform. Manage all GRC work on a single platform. Make better decisions. Collaborate Bring together all departments wherever they may be located. Address the requirements of the entire user community. Allow for painless collaboration between executives, process users, administrators and IT teams. Deploy Cloud-based or On-Premise, deploy and start using within days. Migrate your existing data and integrate with systems such as SAP, Oracle, Microsoft 365. Customize Adapt to the evolving changes of your growing organization and address the unique business needs of each unit. Tailor-made customization is possible within weeks. The flexibility and the ease of user customization we offer is unmatched. Scale Scale up or across using our modules to respond easily to organizational shifts, competitive threats, industry innovations and governmental mandates. Integrate Integrate with AuditRunner open API with 3rd Party apps like, Okta, Office, SAP, Google... Features of AuditRunner include risk management, business process management, management response action planning, process cataloging, survey, meeting administration, ethical breach reporting, and information asset inventory control and incident management among others. Enterprises can utilize assessment capabilities to conduct analysis and define process-specific risk tolerance, accredited certification standards, audit criteria, action plans, and key performance indicators. It also lets teams catalog governing standards, compose regulatory checklists, and ensure data protection in compliance with GDPR and CCPA regulations. Below AuditRunner Modules can be integrated to manage all GRC functions or can be acquired separately as needed: *Internal Audit Administer all your internal audit activities on AuditRunner’s process-based, risk-oriented internal audit module. In line with IIA standards. Link Audit Activity to any Standard or Regulation and avoid duplicate audits. *Risk Management Associate risks with control points, accredited certification standards and governing regulations, along with information inventory assets. Allows for ISO 31000 Accreditation. *Internal Controls Define Controls for any process of any department, with control description, control target, key control, control function, automation and frequency details. In line with COSO 2013 Framework. *Quality Assurance Manage Quality accreditation through audit activities, corrective, and preventive actions and registering customer complaints. *Compliance Audit With our Criteria based audit architecture execute audit activities for any regulation, collect findings and generate custom reports automatically. *Regulatory Compliance Compose your regulatory checklist, define obligations, associated with risks and assign action plans to business units. *Data Protection Compliance Ensure compliance with Data Protection Regulations. Compile Personal Data Inventory. Compose data breach reaction plans and manage data destruction policies. *Business Continuity Compliance Execute Business Impact Analysis and ensure compliance with ISO 22301 Business Continuity Management Standard. *Information Asset Inventory Compile Information Asset Inventory, ensure compliance with ISO 27001 Information Security Management Standard. *Process Catalog Compile all internal company processes along with associated documents, flow charts, and other GRC elements. *Regulation & Standards Catalog Compile all governing regulations and standards along with associated documents, literature, and other GRC elements. *Business Process Management (BPM) Modeling Model flow charts of processes with BPMN2 notation, create RACI and SIPOC matrices, associate attributes such as risks, controls, info assets. *Document Management Create, manage, revise and distribute all internal documentation on a single platform using the advanced document manager and text editor. *Enterprise Repository Automatic audit trail feature keeps track of action and time details of all tasks and applications on the platform. Compile all documentation with revision details. *Action Plan Follow-Up Report and track progress of all action plans created for findings, nonconformities, regulations, and manual entries on all AuditRunner modules. *Certification Management *Meeting Management *Training&Survey *Ethical Breach Reporting *Carbon Footprint Calculator

Average Rating: 4.5/5.0

Total Reviews: 26

How Do G2 Users Rate AuditRunner?

  • Has the product been a good partner in doing business?: 9.5/10 (Category avg: 9.1/10)
  • Corrective Actions: 9.2/10 (Category avg: 8.8/10)
  • Conformance Records: 9.4/10 (Category avg: 8.9/10)
  • Flexibility: 8.9/10 (Category avg: 8.6/10)

Who Is the Company Behind AuditRunner?

  • Seller: WorkRunner
  • Year Founded: 2017
  • HQ Location: Menlo Park, US
  • Twitter: @workrunner
    4 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    4 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Insurance
  • Company Size: 54% Medium, 38% Small

What Do G2 Reviewers Say About AuditRunner?

AI-generated summary from verified user reviews

Pros
  • Users value the user-friendly and flexible interface of AuditRunner, facilitating efficient internal audit workflow automation.
  • Users find AuditRunner very user-friendly, offering an intuitive interface and customizable features for a seamless experience.
  • Users appreciate the automation of internal audit workflows in AuditRunner, enjoying a user-friendly and flexible interface.
  • Users value the user-friendly compliance interface of AuditRunner, facilitating effective audits and risk management processes.
  • Users commend the excellent customer support from AuditRunner, enhancing ease of use and customization capabilities.
Cons
  • Users find the inability to edit or delete fields after saving items frustrating and limiting their data management.
  • Users struggle with the inability to edit or delete fields in AuditRunner, leading to frustration in data management.
  • Users face editing difficulties as some fields cannot be modified or deleted post-save, complicating their workflow.
  • Users face editing limitations in AuditRunner, restricting their ability to modify saved items, affecting flexibility.
  • Users face limited customization options in AuditRunner, restricting their ability to modify saved fields effectively.

What Are Recent G2 Reviews of AuditRunner?

What Are G2 Users Discussing About AuditRunner?

EHSWatch

EHSWatch is an AI-powered, cloud-based Environmental, Health, and Safety (EHS) management software designed to help organizations enhance workplace safety, ensure regulatory compliance, and drive operational excellence. The platform leverages artificial intelligence to streamline EHS processes—covering incident reporting, risk assessment, audits, inspections, corrective actions, and more—all within a single, intuitive system. Built for enterprises across industries such as Oil & Gas, Construction, Manufacturing, Utilities, and Engineering, EHSWatch empowers HSE teams to proactively identify risks, automate corrective actions, and monitor real-time safety performance. Its modern web and mobile applications enable on-site reporting, offline access, and instant visibility into safety and compliance data—anytime, anywhere. EHSWatch’s modular design allows organizations to configure only the features they need, including: AI-driven Incident & Observation Management for faster reporting, automated root-cause analysis, and predictive insights Inspection & Audit Management with digital checklists and automated scoring Risk Assessment to evaluate and mitigate workplace hazards Action & CAPA Tracking for timely closure and accountability Permit-to-Work (PTW) for controlled access and safety assurance EHS KPI Dashboards and Analytics providing actionable, data-driven insights EHSWatch delivers scalable, multi-site support with implementation and customer support teams ensuring seamless onboarding, configuration, and continuous improvement. With its modern interface, mobile-first experience, and AI-driven insights, EHSWatch transforms compliance management into a proactive, intelligent process. Whether your goal is to improve safety culture, reduce risks, or ensure compliance across multiple sites, EHSWatch provides the tools and insights to help organizations operate safely and efficiently.

Average Rating: 4.5/5.0

Total Reviews: 12

How Do G2 Users Rate EHSWatch?

  • Has the product been a good partner in doing business?: 9.2/10 (Category avg: 9.1/10)

Who Is the Company Behind EHSWatch?

Who Uses This Product?

  • Company Size: 67% Medium, 25% Large

What Do G2 Reviewers Say About EHSWatch?

AI-generated summary from verified user reviews

Pros
  • Users appreciate the centralized platform of EHSWatch, which streamlines workflows and improves team communication.
  • Users value the centralized reporting and tracking features of EHSWatch, boosting transparency and team communication.
  • Users value the auditing ease of EHSWatch, appreciating its centralized platform and automated workflows for efficiency.
  • Users value the enhanced communication provided by EHSWatch, which streamlines workflows and increases transparency across teams.
  • Users value the centralized document management of EHSWatch, facilitating efficient compliance and reporting processes.
Cons
  • Users feel that inefficient notifications hinder case management, suggesting improvements for better follow-up reminders.
  • Users desire limited customization options for workflows and fields, hindering their ability to tailor the platform to their needs.
  • Users find the time-consuming setup and customization process frustrating, requiring additional support for user adoption.

What Are Recent G2 Reviews of EHSWatch?

Trackmedium eQMS (Quality Management System)

Trackmedium eQMS is a cloud-based electronic quality management system for regulated manufacturers and other quality-driven organizations. It brings quality, safety and compliance processes into one connected, configurable platform. Modules include Document Control, Training Management, CAPA, Nonconformance, Deviation, Audits, Management of Change, Supplier Management, Equipment Management and Calibration, Incident Management, and Customer Communication and Complaints, plus APQP, PPAP, HACCP, JSA, SDS, Receiving and RMA. Records link across modules, so a nonconformance can lead to a CAPA, an audit finding, a document change and a training assignment, with traceability from start to finish. The platform includes configurable workflows, electronic signatures, audit trails, dashboards and reporting, visual drag-and-drop designers for forms and applications, single sign-on and supplier access. Trackmedium AI gives users an in-app assistant, with controls to enable, limit or disable it by role. Trackmedium eQMS supports the requirements of ISO 9001, ISO 13485, ISO 14001, IATF 16949 and FDA 21 CFR Part 11. Compliance itself is achieved through your validated implementation and procedures.

Average Rating: 4.8/5.0

Total Reviews: 6

How Do G2 Users Rate Trackmedium eQMS (Quality Management System)?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)
  • Corrective Actions: 10.0/10 (Category avg: 8.8/10)
  • Conformance Records: 10.0/10 (Category avg: 8.9/10)
  • Flexibility: 10.0/10 (Category avg: 8.6/10)

Who Is the Company Behind Trackmedium eQMS (Quality Management System)?

  • Seller: Trackmedium
  • Company Website:
  • Year Founded: 2018
  • HQ Location: Riverside, US
  • LinkedIn® Page: www.linkedin.com
    9 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 50% Medium, 50% Small

What Do G2 Reviewers Say About Trackmedium eQMS (Quality Management System)?

AI-generated summary from verified user reviews

Pros
  • Users find the excellent customer support invaluable, especially during the onboarding process for Trackmedium eQMS.
  • Users appreciate the ease of use of Trackmedium eQMS, finding it highly functional and enjoyable to navigate.
  • Users commend the flexibility of Trackmedium eQMS, fulfilling their diverse requirements effectively and enhancing their experience.
  • Users value the high functionality and module integration of Trackmedium eQMS, enhancing their overall user experience.
Cons
  • Users find the documentation inadequate for reports, though support responds promptly when additional information is requested.
  • Users find the reporting issues frustrating but appreciate the quick responses when requesting additional information.

What Are Recent G2 Reviews of Trackmedium eQMS (Quality Management System)?

Qualcy Enterprise Quality Management System (EQMS)

Qualcy Bio-Med eQMS Software has been designed for Bio-Medical companies (including Biotech, Pharma and Medical Device) to manage QMS records for ISO13485, FDA, EU MDR requirements. * Designed for meeting the requirements for 21 CFR Part 820 * Has built in features for E-sign, audit trails and complies with 21 CFR part 11 requirements. This software helps manage the records for Doc. change control, complaints, audits, CAPA, NC Records, Training Records and more.

Average Rating: 4.7/5.0

Total Reviews: 5

How Do G2 Users Rate Qualcy Enterprise Quality Management System (EQMS)?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)
  • Corrective Actions: 10.0/10 (Category avg: 8.8/10)
  • Conformance Records: 10.0/10 (Category avg: 8.9/10)
  • Flexibility: 10.0/10 (Category avg: 8.6/10)

Who Is the Company Behind Qualcy Enterprise Quality Management System (EQMS)?

  • Seller: Qualcy Systems
  • Year Founded: 2014
  • HQ Location: San Diego, US
  • Twitter: @QualcySystems
    1 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    7 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 80% Small, 20% Large

What Are Recent G2 Reviews of Qualcy Enterprise Quality Management System (EQMS)?

isoTracker

isoTracker is a cloud-based Quality Management System (QMS) solution designed to assist small to medium-sized businesses in achieving compliance with various quality management standards. This software provides an accessible platform for organizations looking to streamline their quality processes, ensuring adherence to critical regulations such as ISO 9001, ISO 14001, ISO 17025, ISO 13485, ISO 45001, and ISO 22000. With no set-up costs and proactive support, isoTracker is tailored to meet the needs of businesses aiming to enhance their quality management practices without incurring significant upfront investments. Targeted primarily at small to medium-sized enterprises, isoTracker offers a flexible and user-friendly interface that simplifies the complexities of quality management. Its cloud-based nature allows users to access the system from anywhere, facilitating collaboration among teams and ensuring that quality processes are maintained consistently across various locations. This is particularly beneficial for businesses that operate in multiple regions or have remote teams, as it enables real-time updates and communication regarding quality standards and compliance. The software is designed to support a wide range of use cases, from document control and audit management to risk assessment and corrective action tracking. Each feature is crafted to help organizations maintain compliance and improve their overall quality management processes. For instance, the document control feature allows users to manage and track changes to critical documents, ensuring that all team members are working with the most current information. Additionally, the audit management functionality helps businesses prepare for internal and external audits, making it easier to demonstrate compliance with industry standards. Key features of isoTracker include its validation to FDA 21 CFR Part 11, EU Annex 11, and EU GMP, which ensures that the software meets stringent regulatory requirements. This validation is crucial for businesses operating in regulated industries, as it provides assurance that the software can support their compliance efforts effectively. Furthermore, the pay-as-you-go model allows organizations to select and pay only for the features they need, making it a cost-effective solution that can grow alongside their business. Overall, isoTracker stands out in the QMS software category by offering a comprehensive, flexible, and compliant solution that addresses the specific needs of small to medium-sized businesses. Its proactive support and user-friendly design make it an invaluable tool for organizations striving to enhance their quality management systems while ensuring compliance with essential standards and regulations.

Average Rating: 4.6/5.0

Total Reviews: 4

How Do G2 Users Rate isoTracker?

  • Corrective Actions: 10.0/10 (Category avg: 8.8/10)
  • Conformance Records: 10.0/10 (Category avg: 8.9/10)

Who Is the Company Behind isoTracker?

Who Uses This Product?

  • Company Size: 25% Large, 25% Medium

What Do G2 Reviewers Say About isoTracker?

AI-generated summary from verified user reviews

Pros
  • Users value the excellent customer support from isoTracker, enhancing their experience with the product significantly.
  • Users praise isoTracker for its effective document management tools that simplify versioning of critical documents.
  • Users value isoTracker's cloud-based accessibility, simplifying their quality management system and enhancing overall usability.
  • Users find isoTracker's ease of use exceptional, especially with its simple setup and helpful demo resources.
  • Users enjoy the easy access of isoTracker, benefiting from cloud-based solutions that enhance flexibility and convenience.

What Are Recent G2 Reviews of isoTracker?

What Are G2 Users Discussing About isoTracker?

Appward

Software companies don’t understand your business. From one group you get a rigid solution that requires expensive and time-consuming implementation. From the other you get a hodgepodge of disconnected applications. We feel your pain. Appward delivers a smart set of over 80 apps in a blazing-fast private workspace that helps you manage and improve every function in your organization, including project management, CRM, employee management, operations, quality, manufacturing and supply chain.

Average Rating: 4.5/5.0

Total Reviews: 12

How Do G2 Users Rate Appward?

  • Has the product been a good partner in doing business?: 8.7/10 (Category avg: 9.1/10)

Who Is the Company Behind Appward?

  • Seller: Appward
  • Year Founded: 2021
  • HQ Location: Santa Clarita, US
  • Twitter: @AppwardSocial
    2 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    18 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 58% Medium, 37% Small

What Do G2 Reviewers Say About Appward?

AI-generated summary from verified user reviews

Pros
  • Users value the ease of use of Appward, which simplifies setup, reporting, and enhances team collaboration efficiently.
  • Users appreciate the efficiency of Appward, benefiting from fast access to integrated functionalities and streamlined project management.
  • Users value the focus on real growth and monetization of Appward, enhancing engagement and performance significantly.
  • Users admire the focus on real growth and monetization that Appward offers, enhancing engagement and retention effectively.
  • Users love the intuitive design of Appward, enabling quick access to essential tools and improving collaboration significantly.
Cons
  • Users find the learning curve challenging, as features lack clarity and require significant effort to master.
  • Users find feature limitations in Appward, noting the lack of customization and advanced targeting options.
  • Users find Appward has limited customization, which restricts advanced targeting for complex campaigns and strategies.
  • Users find Appward has limited features, lacking customization and mobile app options, hindering complex campaign execution.
  • Users find Appward's missing features limit customization and targeting, impacting complex campaign execution and mobile usability.

What Are Recent G2 Reviews of Appward?

Panotica Hydra

Panotica Hydra 4.0 is a smart web-based software dedicated for companies with implemented Quality Management System that is compliant with ISO 9001 or other similar ones. The software allows not only to gather all of the companys improvement processes in one system, but also to actively integrate all of the employees on the system platform. Hydra provides access to supervise activities remotely aimed at improving quality as well as engages companys employees in the improvement process. MODULAR STRUCTURE - customized to your specific needs. ONLINE DOCUMENT EDITOR - view and edit your Office documents online. 5 WHY ANALYSIS - easily find the causes of the problem. SWOT ANALYSIS - strengths, weaknesses, opportunities, and threats.

Average Rating: 5.0/5.0

Total Reviews: 3

How Do G2 Users Rate Panotica Hydra?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)
  • Corrective Actions: 10.0/10 (Category avg: 8.8/10)
  • Conformance Records: 10.0/10 (Category avg: 8.9/10)

Who Is the Company Behind Panotica Hydra?

  • Seller: Galactica
  • Year Founded: 2005
  • HQ Location: Bydgoszcz, PL
  • LinkedIn® Page: www.linkedin.com
    15 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 67% Medium, 33% Small

What Are Recent G2 Reviews of Panotica Hydra?

What Are G2 Users Discussing About Panotica Hydra?

Q-Hub

Q-Hub is a modern eQMS and QHSE platform built for compliance-heavy teams that need to move beyond spreadsheets. Q-hub headquarters are in the UK but service customers world wide. Q-Hub helps organisations align to ISO standards while reducing manual admin and improving audit readiness across quality, health & safety and environmental management. Configure ISO-ready workflows for document control, audits, CAPA, incidents and training in minutes—no code required. Centralise policies, procedures and SOPs with version control and Read & Acknowledge features and scheduled reviews. Plan audits, raise NCRs from failed checks, and digitise inspections with smart forms that work offline for shop-floor and field teams. Link assets to calibration and maintenance schedules with automatic reminders, and track everything through role-based dashboards and live KPIs. Q-hub is ideal for manufacturers, aerospace, automotive, food production and multi-site operations needing a eQMS, ISO, HSE and audit management system in one easy to use cloud platform.

Average Rating: 4.8/5.0

Total Reviews: 3

How Do G2 Users Rate Q-Hub?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)
  • Corrective Actions: 10.0/10 (Category avg: 8.8/10)
  • Conformance Records: 10.0/10 (Category avg: 8.9/10)
  • Flexibility: 6.7/10 (Category avg: 8.6/10)

Who Is the Company Behind Q-Hub?

Who Uses This Product?

  • Company Size: 100% Medium

What Are Recent G2 Reviews of Q-Hub?

tracezilla

tracezilla is ERP software designed for food companies and for companies within pharma logitics. tracezilla offers a standard solution with a high level of flexibility supporting advanced flows and complex business models. In tracezilla, traceability and compliance is at the core with features designed to meet the requirements within the food and beverage, and pharma logistics sectors. tracezilla handles purchase, production, sales, logistics, inventory, forecasting, quality, financials, documentation and reporting and much more. tracezilla is targeted SME companies in all countries.

Average Rating: 4.8/5.0

Total Reviews: 3

How Do G2 Users Rate tracezilla?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)
  • Flexibility: 5.0/10 (Category avg: 8.6/10)

Who Is the Company Behind tracezilla?

  • Seller: tracezilla
  • Year Founded: 2018
  • HQ Location: Lystrup, DK
  • LinkedIn® Page: www.linkedin.com
    9 employees on LinkedIn®
  • Phone: +4581111034

Who Uses This Product?

  • Company Size: 67% Small, 33% Medium

What Are Recent G2 Reviews of tracezilla?

LabCollector LIMS & ELN

LabCollector is a comprehensive laboratory management software solution designed to streamline and enhance the organization, centralization, and tracking of reagents, samples, tests, experiments, workflows, lab data, and processes. This software is tailored for laboratories seeking to maintain full compliance with ISO and FDA standards, ensuring that all operations are conducted within regulatory guidelines. Targeted at a diverse audience that includes research institutions, clinical laboratories, and pharmaceutical companies, LabCollector provides an adaptable platform that meets the varied needs of laboratory professionals. Its modular design allows users to customize the software according to their specific requirements, making it suitable for small labs as well as larger research facilities. The software supports a wide range of use cases, from tracking sample integrity and managing reagent inventories to automating complex workflows and ensuring data accuracy across various laboratory processes. One of the standout features of LabCollector is its ability to connect with any type and brand of laboratory instruments, including balances, analyzers, diagnostics, and chromatography systems. This connectivity enables users to build secure automation workflows that enhance data integrity and reduce the potential for human error. Additionally, the software's integration capabilities extend to various enterprise systems, such as ERP, CRM, QMS, and EMR/EHR, through simple HL7, XML, and CSV file exchanges, as well as API connections and data mapping. This flexibility allows laboratories to maintain seamless operations and data flow across different platforms. LabCollector also includes proactive alert and notification features that keep users informed about important aspects of their laboratory operations. Users receive timely reminders regarding equipment maintenance, warranty status, and the expiration or quantity of reagents and samples. This functionality not only helps in maintaining optimal laboratory conditions but also aids in inventory management, ensuring that critical resources are always available when needed. Overall, LabCollector stands out in the laboratory management software category by offering a robust, flexible, and user-friendly solution that adapts to the evolving needs of laboratories. Its comprehensive features, combined with the ability to integrate with existing systems and automate workflows, make it an invaluable tool for enhancing laboratory efficiency and compliance.

Average Rating: 4.2/5.0

Total Reviews: 11

How Do G2 Users Rate LabCollector LIMS & ELN?

  • Has the product been a good partner in doing business?: 8.7/10 (Category avg: 9.1/10)
  • Conformance Records: 8.3/10 (Category avg: 8.9/10)
  • Flexibility: 6.7/10 (Category avg: 8.6/10)

Who Is the Company Behind LabCollector LIMS & ELN?

  • Seller: AgileBio
  • Year Founded: 2002
  • HQ Location: PARIS, FR
  • Twitter: @agilebio
    323 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    16 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 73% Small, 18% Medium

What Do G2 Reviewers Say About LabCollector LIMS & ELN?

AI-generated summary from verified user reviews

Pros
  • Users find LabCollector LIMS & ELN to be super user-friendly, allowing seamless adaptation to their specific lab needs.
  • Users value the robust data storage of LabCollector LIMS & ELN, enabling efficient management of extensive information.
  • Users appreciate the robust data management of LabCollector LIMS & ELN, ensuring consistency and effective sample submission handling.
  • Users appreciate the flexibility of LabCollector, enabling customization to meet specific lab needs and improve efficiency.
  • Users appreciate the customization and reliability of LabCollector LIMS & ELN, meeting their specific lab needs effectively.
Cons
  • Users face challenges with poor customer support, experiencing delays and limited assistance through email and ticketing systems.
  • Users report UX improvement issues, including slow indexing, navigation challenges, and limited customer support efficiency.
  • Users report data inaccuracy issues, struggling with slow indexing and data management inefficiencies in LabCollector.
  • Users experience slow indexing and poor data management, making navigation and efficient operations challenging.
  • Users find difficult navigation in LabCollector LIMS & ELN, hindering efficient data management and functionality.

What Are Recent G2 Reviews of LabCollector LIMS & ELN?

monitorQA

Mobile inspection software for monitoring compliance, health, and safety in the workplace.

Average Rating: 4.8/5.0

Total Reviews: 2

How Do G2 Users Rate monitorQA?

  • Has the product been a good partner in doing business?: 8.3/10 (Category avg: 9.1/10)

Who Is the Company Behind monitorQA?

Who Uses This Product?

  • Company Size: 100% Small

What Do G2 Reviewers Say About monitorQA?

AI-generated summary from verified user reviews

Pros
  • Users find MonitorQA incredibly easy to use, streamlining their workflow and eliminating time-consuming manual work.
  • Users praise the exceptional customer support of MonitorQA, valuing their proactive approach and responsiveness to feedback.
  • Users appreciate the exceptional support from MonitorQA, noting their proactive approach to enhancements and user feedback.
  • Users find the setup ease of MonitorQA impressive, allowing for a straightforward and seamless experience.
  • Users find that MonitorQA helps them save time on manual work, enhancing their overall efficiency in service updates.
Cons
  • Users find the slow loading of some endpoints affects the overall experience, despite the product's strong features.

What Are Recent G2 Reviews of monitorQA?

Nulogy Quality & Compliance

Nulogy Quality & Compliance runs audits, inspections, non-conformances, CAPA, EHS, supplier compliance, and FSMA 204 traceability in one system. Quality and safety teams stop assembling evidence the week before the auditor arrives, because the evidence is captured as the work happens. It's built for quality directors, FSQA managers, and EHS leads running multi-site manufacturing and food distribution operations. North America's largest food distributor runs FSQA oversight across 180+ sites on it. WHAT'S INSIDE Audits and inspections Plan audits and capture checks, photos, and evidence on the line with iOS and Android apps that work offline when the plant floor has no signal. Build and version your own templates for BRCGS, SQF, FSSC 22000, ISO 9001, IATF 16949, ISO 45001, and customer-specific programs. Non-conformance and CAPA Raise an NCR straight from a failed check, assign an owner and a due date, and track corrective and preventive action through to verified closure. Overdue actions trigger reminders, so nothing sits open until the next audit finds it. EHS Incident and near-miss reporting, permits, contractor management, and training and competency records across every site. Document control Version management, e-signature, and approval routing, so the procedure on the line is the current one. Multi-site reporting Audit results, open actions, and trends by site, line, and supplier, with a full audit trail behind every record. Track & Trace for FSMA 204 Nulogy Track & Trace turns the shipping, receiving, and transformation events already flowing through your ERP, WMS, and shop floor into a searchable register of Critical Tracking Events. Traceability Lot Codes are generated and linked automatically, including when lots are combined or repacked. When the FDA asks, you produce the sortable electronic spreadsheet for any lot, product, date range, or trading partner in minutes. The FDA gives you 24 hours. The compliance date is July 20, 2028. Supplier Compliance Supplier approval, certificate capture with expiry tracking, supplier scorecards, and supplier non-conformances in one place, instead of a shared inbox and a spreadsheet. PART OF THE NULOGY MANUFACTURING OPERATING SYSTEM (MOS) Quality & Compliance connects to Nulogy Smart Factory and Shop Floor. A scrap or defect event captured in Smart Factory can open an NCR and start a 5-Why or CAPA workflow in Quality & Compliance automatically. INDUSTRIES Food and beverage manufacturing, foodservice distribution, contract packaging and manufacturing, automotive, industrial manufacturing, packaging, and 3PL.

Average Rating: 4.7/5.0

Total Reviews: 9

How Do G2 Users Rate Nulogy Quality & Compliance?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)

Who Is the Company Behind Nulogy Quality & Compliance?

  • Seller: Nulogy
  • Company Website:
  • Year Founded: 2002
  • HQ Location: Toronto, CA
  • Twitter: @nulogy
    1,022 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    119 employees on LinkedIn®

Who Uses This Product?

  • Company Size: 50% Small, 40% Medium

What Do G2 Reviewers Say About Nulogy Quality & Compliance?

AI-generated summary from verified user reviews

Pros
  • Users value the audit efficiency of AuditComply, effectively tracking compliance, risks, and generating insightful reports.
  • Users value the robust compliance tracking features of AuditComply, enhancing their risk management capabilities effectively.
  • Users value the data analytics capabilities of AuditComply, enhancing compliance tracking and risk management efficiency.
  • Users commend the robust data management features of AuditComply, enabling effective tracking of compliance and risk analytics.
  • Users value the data tracking capabilities of AuditComply, enhancing compliance oversight and risk management effectively.

What Are Recent G2 Reviews of Nulogy Quality & Compliance?

What Are G2 Users Discussing About Nulogy Quality & Compliance?

Daniel Rivera
DR
Researched and written by Daniel Rivera
Updated October 16, 2026