Best Quality Management Systems (QMS) for Small Business

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

Total Products under this Category: 399

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
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Last updated: October 01, 2026

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

Why You Can Trust G2's Software Rankings:

  • 30 Analysts and Data Experts
  • 9,800+ Authentic Reviews
  • 399+ 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: Qualio, Greenlight Guru Quality Management System, Redzone, Arena PLM & QMS, Octave Reliance (ETQ Reliance), QT9 QMS, Mitti (by SafetyCulture), and Ideagen Quality Management.

Underlying data: [Grid® JSON](https://www.g2.com/categories/quality-management-qms/grids.json?focus%5B%5D=qualio&focus%5B%5D=greenlight-guru-quality-management-system&focus%5B%5D=qad-redzone&focus%5B%5D=arena-plm-qms&focus%5B%5D=octave-reliance-etq-reliance&focus%5B%5D=qt9-qms&focus%5B%5D=safetyculturehq&focus%5B%5D=ideagen-quality-management&segment=small-business)

Qualio

Qualio is a quality management and compliance platform built exclusively for life sciences companies. It helps medical device, pharmaceutical, biotech, and digital health organizations accelerate regulatory approvals, stay audit-ready, and scale compliance operations without adding headcount. Our platform manages the full range of quality processes, including document control, training, CAPA, change control, supplier management, risk management, and design controls, all in one validated system, supporting FDA 21 CFR Part 11, ISO 13485, EU MDR, MDSAP, GxP, ICH Q10, and other life sciences requirements. Move faster without compliance as the bottleneck. Qualio connects regulatory affairs, quality, and R&D in one platform, with deep integrations into Jira, Azure DevOps, GitHub, Salesforce, and other tools teams already use, removing the handoffs and manual documentation that typically slow product development down. Get to market faster. Automated gap analysis and multi-framework compliance mapping cut audit preparation time by 80%. Reusing evidence across FDA, ISO, and EU submissions has helped customers shrink market entry timelines from 9 months to 3-4 months, while cross-mapped documentation accelerates 510(k) submissions, CE marking, and international expansion. Scale without growing your compliance overhead. Customers report a 99% reduction in quality administrative time and have eliminated $150K-$300K in annual consulting costs by replacing manual processes, driving 5X ROI within 2 months. See risk before it becomes a finding. End-to-end traceability connects requirements, risk assessments, CAPAs, and product changes, with risk-based alerting that flags gaps before they turn into FDA 483 observations, warning letters, or audit findings. Customers have passed ISO 13485 certifications and sponsor audits with zero major nonconformances using this always-on monitoring. Qualio serves life sciences companies from pre-market startups to established enterprises, with the SOC 2, HIPAA, and pharmacovigilance capabilities growth-stage companies need, deploying faster than legacy eQMS vendors while maintaining the validation rigor required for FDA inspections and notified body audits.

Average Rating: 4.4/5.0

Total Reviews: 775

How Do G2 Users Rate Qualio?

  • Has the product been a good partner in doing business?: 9.1/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.5/10 (Category avg: 8.8/10)
  • Conformance Records: 8.7/10 (Category avg: 8.9/10)
  • Flexibility: 8.4/10 (Category avg: 8.6/10)

Who Is the Company Behind Qualio?

  • Seller: Qualio
  • Company Website:
  • Year Founded: 2012
  • HQ Location: San Francisco, California
  • Twitter: @qualiohq
    711 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    124 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Manager, Clinical Data Associate
  • Top Industries: Medical Devices, Pharmaceuticals
  • Company Size: 52% Medium, 40% Small

What Do G2 Reviewers Say About Qualio?

AI-generated summary from verified user reviews

Pros
  • Users find Qualio to be incredibly easy to use, enhancing the training experience with its intuitive interface.
  • Users appreciate the user-friendly training modules of Qualio, which enhance efficiency and simplify tracking training progress.
  • Users value the extremely searchable document management system in Qualio, enhancing control and ease of use.
  • Users appreciate the efficient document control of Qualio, enhancing organization and simplifying the approval process.
  • Users love Qualio's intuitive interface, making it easy to navigate, learn, and improve collaboration effectively.
Cons
  • Users find document update triggers problematic due to multiple change requests, creating complexity in document management.
  • Users express frustration over feature limitations in Qualio, affecting access, updates, and overall experience.
  • Users find difficult usability in Qualio, particularly with editing older document versions and feedback on answers.
  • Users find Qualio's interface not user-friendly, citing rigidity and limited customization options that hinder their experience.
  • Users face editing difficulties with table formatting and lack timely notifications for overdue document reviews in Qualio.

What Are Recent G2 Reviews of Qualio?

What Are G2 Users Discussing About Qualio?

Greenlight Guru Quality Management System

Greenlight Guru is the #1 quality management system built exclusively for medical device companies. Not life sciences. Not pharma with a medtech configuration layer. Because we built exclusively for medical devices, ISO 13485, ISO 14971, and FDA QMSR aren't frameworks you configure after the fact. They're the foundation. Most quality teams manage compliance across systems that were never designed to talk to each other. A document control tool here, a spreadsheet for CAPAs there, a separate process for change control. In a regulated environment, that gap doesn't stay invisible, it shows up during audits. Greenlight Guru gives Quality and Product teams a single connected system where document control, training, CAPA, nonconformance, change control, supplier management, risk management, and design controls work together. When a change happens, it flows through the workflow. Meaning limited manual handoffs, and nothing falling through the cracks between teams. For Quality and Regulatory Affairs professionals, that means audit-ready workflows with automated routing, electronic signatures, and complete audit trails built in, including end-to-end traceability across design controls. No more chasing approvals or manually tracking compliance status. Teams that run on Greenlight Guru are 3.5x less likely to receive a major audit finding. For R&D and product teams, it means staying in the tools they already use, with changes automatically syncing to design controls so documentation builds itself as you work, not after the fact as a separate project. Greenlight Guru AI handles the repetitive work that slows teams down, and it was built with 15 years of medtech context behind it, not bolted on from a general-purpose model. AI-powered search finds answers across your QMS instantly. Chat analyzes system data to surface insights. Auto-generated summaries give immediate context on documents, suppliers, and quality events. For product teams, verifiability checks catch vague requirements before they become audit findings, suggested links close traceability gaps automatically, and AI brainstorming gets engineers moving faster. For quality teams, AI generates training quizzes and drafts change order summaries, so your team spends less time writing and more time on the work that actually requires their expertise. The platform is validated out of the box and aligned to FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, EU MDR, and FDA 21 CFR Part 11. Implementation is measured in weeks, not the quarters-long projects that come with legacy enterprise platforms. Backed by 80+ audit-tested, customizable templates and a team of experts who know medtech inside and out. You're not managing a separate validation project before you can go live. For 15 years and across more than 1,000 device companies worldwide, Greenlight Guru has been the QMS medical device teams trust to pass audits, bring products to market, and stay on the market longer.

Average Rating: 4.5/5.0

Total Reviews: 421

How Do G2 Users Rate Greenlight Guru Quality Management System?

  • Has the product been a good partner in doing business?: 9.3/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.6/10 (Category avg: 8.8/10)
  • Conformance Records: 8.7/10 (Category avg: 8.9/10)
  • Flexibility: 8.0/10 (Category avg: 8.6/10)

Who Is the Company Behind Greenlight Guru Quality Management System?

  • Seller: Greenlight Guru
  • Company Website:
  • Year Founded: 2013
  • HQ Location: Indianapolis, IN
  • Twitter: @greenlightguru
    10,590 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    135 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Manager, CEO
  • Top Industries: Medical Devices, Biotechnology
  • Company Size: 77% Small, 20% Medium

What Do G2 Reviewers Say About Greenlight Guru Quality Management System?

AI-generated summary from verified user reviews

Pros
  • Users highlight the ease of use of Greenlight Guru, appreciating its intuitive design and excellent support.
  • Users find Greenlight Guru's features enhance functionality, making compliance management streamlined and easy to use.
  • Users value the effective training tools provided by Greenlight Guru, facilitating quick and straightforward implementation.
  • Users appreciate the streamlined audit management in Greenlight Guru, facilitating compliance and organization effortlessly.
  • Users value the configurability of Greenlight Guru, enhancing compliance and streamlining quality management processes efficiently.
Cons
  • Users find the pricing to be uncompetitive, especially when faced with additional charges for extra projects.
  • Users find the feature limitations frustrating, particularly with inflexible quality events and costly additional projects.
  • Users find the search function inefficient, wishing for improvements like AI to enhance information retrieval.
  • Users find the inflexibility of quality events frustrating, though the system meets necessary CAPA requirements.
  • Users find analytics to be limited, which restricts valuable data insights and overall functionality.

What Are Recent G2 Reviews of Greenlight Guru Quality Management System?

What Are G2 Users Discussing About Greenlight Guru Quality Management System?

Redzone

Redzone is the #1 connected workforce solution on a mission to empower frontline teams with AI-powered manufacturing software. As a whole-plant solution, it digitizes and simplifies work for production, maintenance, and quality teams on a single platform, focusing on manufacturers' strategic goals for deployment. Factories using Redzone connect and engage the frontline, equipping them with communication, collaboration, and AI tools specifically designed for manufacturing. Redzone Productivity Solutions Redzone empowers manufacturers with a comprehensive suite designed to enhance efficiency through Champion AI. Our solutions include: * OEE Monitoring: Track and optimize Overall Equipment Effectiveness in real time * Real-Time Dashboards: Gain immediate visibility into operations * Communication Tools: Facilitate collaboration with chats, huddles, and collaboration, all with live translation capabilities * Action Management: Streamline task execution and follow-up * Continuous Improvement (CI) Routines: Foster ongoing operational enhancements By leveraging these tools, manufacturers can enhance processes, drive digital and lean transformations, enable paperless quality and compliance, execute Total Productive Maintenance (TPM) programs, and accelerate frontline training and onboarding. Key Benefits * 26% Productivity Improvement: Achieve this in just 90 days, with ROI in 3 to 6 months * 81% Increase in Frontline Engagement: Supported by our connected Learning Management System, along with a 35% reduction in employee turnover * 24% Reduction in Unplanned Downtime: Enabled by our connected Computerized Maintenance Management System (CMMS) * Stay Audit-Ready: Always prepared with our connected Quality Management System (QMS) Who We Serve Redzone supports over 2000 global manufacturers, enhancing engagement and purpose among hundreds of thousands of frontline workers across sectors, including Food & Beverage, CPG, Automotive, Pharmaceuticals, and Industrial. Platform Redzone is a mobile-first solution (iOS, Android, Google) designed for the plant floor, featuring TV display capabilities for real-time visibility. Reporting and administration are browser-based and accessible on any device. Integrations Redzone seamlessly integrates with ERP systems like SAP, S4Hana, Oracle, D365, Sage X3, and QAD, as well as CMMS, MES, EAM, and QMS platforms via standard API integration. Company Overview: Redzone, a subsidiary of QAD, is a privately held company headquartered in Miami, Florida. We serve manufacturers worldwide, providing innovative solutions to enhance operational efficiency and productivity.

Average Rating: 4.8/5.0

Total Reviews: 628

How Do G2 Users Rate Redzone?

  • Has the product been a good partner in doing business?: 9.6/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.3/10 (Category avg: 8.8/10)
  • Conformance Records: 9.3/10 (Category avg: 8.9/10)
  • Flexibility: 9.4/10 (Category avg: 8.6/10)

Who Is the Company Behind Redzone?

  • Seller: QAD
  • Company Website:
  • Year Founded: 1979
  • HQ Location: Santa Barbara, CA
  • Twitter: @QAD_Community
    3,248 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    1,563 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Plant Manager, Continuous Improvement Manager
  • Top Industries: Food Production, Food & Beverages
  • Company Size: 79% Medium, 11% Large

What Do G2 Reviewers Say About Redzone?

AI-generated summary from verified user reviews

Pros
  • Users find RedZone's ease of use notable, facilitating quick onboarding and effective team communication.
  • Users value the effective plant-wide communication in Redzone, enhancing team support and operational efficiency.
  • Users praise the efficiency improvement with Redzone, noting quick processes and effective team communication.
  • Users value the expert coaching support provided by Redzone, ensuring quick adaptation and effective implementation for teams.
  • Users value the significant productivity improvement Redzone provides through real-time data and efficient communication tools.
Cons
  • Users find the learning curve steep, as mastering features and setup requires time and adjustments for optimal use.
  • Users struggle with the platform compatibility of Redzone, wishing for broader support beyond just iOS devices.
  • Users find the complex setup of RedZone to be time-consuming and frustrating, impacting overall usability.
  • Users find data management limitations in Redzone frustrating, as it complicates compliance and customization processes.
  • Users express frustration with limited features in Redzone, affecting functionality and integration with maintenance processes.

What Are Recent G2 Reviews of Redzone?

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Arena PLM & QMS

Arena by PTC is a cloud-native product lifecycle management (PLM) and quality management system (QMS) that unifies product and quality information in a secure, single source of truth. By hosting all electrical, mechanical, and software information in a centralized product record, Arena enables every participant throughout the entire product lifecycle to work together anytime and anywhere, increasing visibility and traceability. This accelerates new product development (NPD) and new product introduction (NPI) by streamlining processes, automating review cycles, and reducing errors. Arena PLM keeps internal teams and supply chain partners on the same page. Our scalable and collaborative platform streamlines engineering change reviews, simplifies bill of materials (BOM) management and document control, mitigates supply chain risk, and helps speed product launches. Arena QMS connects quality and product record information into a single, secure system. Easily traceable closed-loop quality and product processes help you introduce high-quality products to market while ensuring compliance with quality standards and regulations, such as FDA 21 CFR Part 820, FDA 21 CFR Part 11, ISO 13485, and AS 9100. Arena Supply Chain Intelligence (SCI) provides real-time electronic component risk and compliance information to reduce supply chain risk throughout NPI and NPD. With Arena SCI embedded within Arena PLM, you can proactively monitor the health of your BOM, identify component issues before they impact production, mitigate risks throughout the product lifecycle, and ensure electronic component compliance as regulatory requirements evolve. Arena’s AI capabilities create smarter, more personalized experiences that empower every customer while adhering to its responsible AI policies. Arena AI Assistant uses a conversational interface to help users navigate Arena with ease and reduce onboarding time, while Arena AI Engine drives faster document reviews and comparisons to further speed workflows. Arena continuously expands its AI capabilities to empower product teams to focus on innovation and execution. Arena supports more than 1,500 complex high-tech electronics, medical device, and aerospace/defense companies around the world. Using Arena’s proven cloud-native solutions, your internal teams and external partners can leverage the most comprehensive product development platform to accelerate product launches while reducing expenses, increasing profitability, and speeding time to market.

Average Rating: 4.2/5.0

Total Reviews: 456

How Do G2 Users Rate Arena PLM & QMS?

  • Has the product been a good partner in doing business?: 8.8/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.3/10 (Category avg: 8.8/10)
  • Conformance Records: 8.3/10 (Category avg: 8.9/10)
  • Flexibility: 7.9/10 (Category avg: 8.6/10)

Who Is the Company Behind Arena PLM & QMS?

  • Seller: PTC
  • Company Website:
  • Year Founded: 1985
  • HQ Location: Boston, Massachusetts
  • Twitter: @PTC
    37,560 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    8,226 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Mechanical Engineer, Engineer
  • Top Industries: Medical Devices, Electrical/Electronic Manufacturing
  • Company Size: 57% Medium, 26% Small

What Do G2 Reviewers Say About Arena PLM & QMS?

AI-generated summary from verified user reviews

Pros
  • Users find Arena PLM & QMS to be user-friendly, with excellent support and seamless integration enhancing their experience.
  • Users value the structured document management in Arena PLM & QMS, enhancing efficiency and compliance in workflows.
  • Users find Arena PLM & QMS's document control system convenient and effective for compliance and workflow management.
  • Users value the ease of use of Arena PLM & QMS, highlighting seamless migrations and responsive support.
  • Users praise the excellent customer support of Arena PLM & QMS, appreciating quick and effective assistance at all times.
Cons
  • Users find feature limitations in Arena PLM & QMS, especially needing extra tools for better tracking and integration.
  • Users identify missing features like auto text and better template creation, hindering efficiency in project tracking.
  • Users find the difficult usability of Arena PLM & QMS frustrating, especially when transitioning from other systems.
  • Users experience limited functionality in Arena PLM & QMS, requiring additional software for effective production tracking.
  • Users find the non-intuitive interface of Arena PLM & QMS frustrating, complicating workflow and navigation.

What Are Recent G2 Reviews of Arena PLM & QMS?

What Are G2 Users Discussing About Arena PLM & QMS?

Octave Reliance (ETQ Reliance)

Octave Reliance® (formerly ETQ Reliance) is the leading provider of quality, EHS and compliance management software, trusted by the world’s strongest brands. More than 600 customers globally, spanning industries such as manufacturing, medical devices, electronics, heavy industry, food and beverage, pharmaceuticals and automotive, use Reliance to secure positive brand reputations, enable higher levels of customer loyalty and enhance profitability. Octave Reliance offers built-in best practices and powerful flexibility to drive business excellence through quality. Reliance QMS provides customers with a suite of fundamental capabilities and a set of core applications that optimize quality management programs: • Document Control • Change Management • Audit Management • Corrective Action (CAPA) • Insights Advanced Analytics • Training Management • Suppliers, Materials and Chemicals • And more Reliance customers have long relied on its comprehensive, cross-industry portfolio of QMS applications to advance their quality programs and meet critical business goals. With Reliance NXG, customers can now accelerate their quality journey into the resilient and adaptable world of cloud-native quality and safety management, advanced analytics, controlled ubiquitous access and enterprise digital transformation. Reliance NXG allows customers to effectively future-proof their quality management systems and provide a powerful catalyst to digital transformation in their organizations. The technological foundation of Reliance NXG is based on four value pillars: usability, flexibility, visibility and scalability, enabled by advanced cloud-native technologies and a transformational vision. • Usability: The solution’s new search capability enables users to quickly find anything within the system, with enhanced navigation to streamline the user experience from any device. • Flexibility: New integration features, built upon a multi-tenant architecture, allow customers to break down the barriers that limit collaboration and keep up with changes in their business. • Visibility: Digital transformation efforts will drive QMS solutions deeper into an organization’s enterprise technology stack. Powered by Insights analytics, workflows can be configured to automatically classify events, improving the speed and accuracy of decisions. Users are provided not just with better information, but also guidance that can be used to streamline investigations and root cause analyses. • Scalability: The cloud-native QMS enables enterprise-wide quality processes, providing support for any number of users, any volume of data and any configuration with a high availability architecture with no single point of failure. Customers in regulated markets can leverage expedited validation and risk-based verification in Reliance to reduce testing effort required. Octave Reliance was originally founded in 1992 as ETQ and has main offices located in the U.S. and Europe. To learn more about Octave Reliance and its various product offerings, visit https://www.octave.com/products/asset-performance-management/reliance.

Average Rating: 4.3/5.0

Total Reviews: 609

How Do G2 Users Rate Octave Reliance (ETQ Reliance)?

  • Has the product been a good partner in doing business?: 8.1/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.4/10 (Category avg: 8.8/10)
  • Conformance Records: 8.3/10 (Category avg: 8.9/10)
  • Flexibility: 7.9/10 (Category avg: 8.6/10)

Who Is the Company Behind Octave Reliance (ETQ Reliance)?

  • Seller: Octave
  • Company Website:
  • HQ Location: Madison, US
  • LinkedIn® Page: www.linkedin.com
    3,835 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Manager, Quality Engineer
  • Top Industries: Medical Devices, Pharmaceuticals
  • Company Size: 50% Large, 41% Medium

What Do G2 Reviewers Say About Octave Reliance (ETQ Reliance)?

AI-generated summary from verified user reviews

Pros
  • Users appreciate the ease of use of Octave Reliance, highlighting simple workflows and effortless user integration.
  • Users value the ease of use and customizable features of ETQ Reliance, enhancing interaction and performance significantly.
  • Users value the customizability of ETQ Reliance, enabling tailored solutions for their unique organizational needs.
  • Users love the customization options with Octave Reliance, enhancing functionality and tailoring the system to their needs.
  • Users value the easy-to-use document management features of Octave Reliance, enhancing performance and interaction with the company.
Cons
  • Users are frustrated by missing features in Octave Reliance, particularly concerning mobile capabilities and access limitations.
  • Users experience feature limitations in ETQ Reliance, particularly with customization, mobile capabilities, and access issues.
  • Users face challenges with limited customization options in ETQ Reliance, making the onboarding and setup processes cumbersome.
  • Users express frustration over the missing functionality in Octave Reliance, impacting usability and training efficiency.
  • Users find the not user-friendly nature of ETQ Reliance frustrating, especially during employee onboarding and workflow setup.

What Are Recent G2 Reviews of Octave Reliance (ETQ Reliance)?

What Are G2 Users Discussing About Octave Reliance (ETQ Reliance)?

QT9 QMS

QT9™ QMS is your all-in-one quality management software. Centralize more quality data metrics than any other platform standard. Easy-to-use & ready-to-go. Fully-validated. Start a trial. All-In-One QMS QT9 provides an integrated solution with 25+ quality modules that include Document Management, Maintenance, Product, Customer, Supplier, Employee Training, ISO, FDA and regulatory compliance automation. Be more efficient with electronic signature approvals, dashboards, automated reminders, multi-site ready, approval management, web portals, user to-do lists and more. Simplify Compliance Make audits easy with one central place to see real-time data for FDA 21 CFR Part 11, FDA 21 CFR Part 210/211, FDA 21 CFR Part 820, ISO 9001, ISO 13485, ISO 14001, ISO 17025, AS9100, HACCP and SQF. Ideal for Life Sciences, Biotechnology, Medical Device Manufacturers, Pharmaceutical Companies, Laboratories, Aerospace and Defense Companies and Foods. Easy-To-Use QT9 QMS is easy to setup and use. See a demo and get started with a free trial today. We offer lots of resources including: QT9 Help, Training Academy, Support Requests, Training Webinars, Content Customization, Free Maintenance, Unlimited Training and Unlimited Support. For more information, visit QT9software.com.

Average Rating: 4.8/5.0

Total Reviews: 127

How Do G2 Users Rate QT9 QMS?

  • Has the product been a good partner in doing business?: 9.6/10 (Category avg: 9.1/10)
  • Corrective Actions: 9.4/10 (Category avg: 8.8/10)
  • Conformance Records: 9.3/10 (Category avg: 8.9/10)
  • Flexibility: 9.0/10 (Category avg: 8.6/10)

Who Is the Company Behind QT9 QMS?

  • Seller: QT9 Software
  • Company Website:
  • Year Founded: 2005
  • HQ Location: Aurora, Illinois
  • Twitter: @Qt9Software
    26 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    69 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Manager, Quality Assurance Manager
  • Top Industries: Medical Devices, Manufacturing
  • Company Size: 55% Medium, 44% Small

What Do G2 Reviewers Say About QT9 QMS?

AI-generated summary from verified user reviews

Pros
  • Users appreciate the intuitive interface of QT9 QMS, enabling quick team adoption and efficient project management.
  • Users praise QT9 QMS for its intuitive setup and task automation, making it ideal for quick implementation.
  • Users commend QT9 QMS for its outstanding customer support, highlighted by responsive and knowledgeable team members who assist promptly.
  • Users appreciate the modular integration of QT9 QMS, enhancing efficiency and supporting seamless quality management across teams.
  • Users value the ease of maintaining audit readiness with QT9, appreciating organized access to critical documents and records.
Cons
  • Users face challenges with setup pre-requisites and control issues, leading to incomplete module implementations in QT9 QMS.
  • Users find the complex setup of QT9 QMS challenging, often requiring extensive time and effort to configure.
  • Users find the difficult usability of QT9 QMS hinders their experience, with complex settings and limited calibration features.
  • Users report feature limitations in QT9 QMS, including restrictions on calibrations and insufficient search functions.
  • Users experience a steep learning curve with QT9 QMS, requiring time and support to navigate the interface effectively.

What Are Recent G2 Reviews of QT9 QMS?

What Are G2 Users Discussing About QT9 QMS?

Mitti (by SafetyCulture)

Mitti (by SafetyCulture) is the operations system for every site, shift and standard. Trusted by over 80,000 organisations, Mitti brings your people, training records and workflows into one operating picture. From the frontline to the boardroom, it gives everyone a clear understanding of who's trained and ready for the shift ahead, highlights what needs attention and recommends what to do next. Every course completed, skill verified and action taken becomes intelligence your teams can use to improve every day.

Average Rating: 4.6/5.0

Total Reviews: 472

How Do G2 Users Rate Mitti (by SafetyCulture)?

  • Has the product been a good partner in doing business?: 9.2/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.4/10 (Category avg: 8.8/10)
  • Conformance Records: 8.4/10 (Category avg: 8.9/10)
  • Flexibility: 9.1/10 (Category avg: 8.6/10)

Who Is the Company Behind Mitti (by SafetyCulture)?

  • Seller: Mitti
  • Company Website:
  • Year Founded: 2004
  • HQ Location: Surry Hills, New South Wales
  • Twitter: @MittiHQ
    4,867 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    428 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Founder, Director
  • Top Industries: Construction, Manufacturing
  • Company Size: 44% Small, 41% Medium

What Do G2 Reviewers Say About Mitti (by SafetyCulture)?

AI-generated summary from verified user reviews

Pros
  • Users value the ease of use of Mitti, enabling quick surveys and reports from any mobile device.
  • Users commend Mitti for its efficiency improvement, significantly streamlining information flow and ensuring timely access to updates.
  • Users value the efficiency of Mitti for streamlining information flow and ensuring timely updates.
  • Users value the customization options of Mitti, enabling easy checklist creation and efficient project management.
  • Users find SafetyCulture's intuitive mobile app enhances usability, streamlining inspections and improving safety management effectively.
Cons
  • Users find missing features in Mitti, such as limited reports and clunky AI, hinder their overall experience.
  • Users find the limited customization in Mitti challenging, particularly with reports and dashboard flexibility.
  • Users struggle with a significant learning curve, finding the interface and AI functionality less intuitive and sometimes clunky.
  • Users express concerns about limited features such as clunky AI functionality and inadequate integration with other tools.
  • Users find the complexity of the interface challenging, leading to a steep learning curve and confusion over features.

What Are Recent G2 Reviews of Mitti (by SafetyCulture)?

What Are G2 Users Discussing About Mitti (by SafetyCulture)?

Ideagen Quality Management

Ideagen Quality Management is a cloud-based quality management system (QMS) that enables quality and operations managers in regulated industries to manage compliance, CAPA workflows, audits, document control and supplier quality across multiple sites from one connected platform. Named a Leader in the Verdantix Green Quadrant 2026, an independent analysis of 14 QMS platforms serving life sciences, healthcare and manufacturing, Ideagen received perfect scores of 3.0/3.0 for AI operations and supplier quality management. AI is embedded into quality workflows from the ground up, not added as a feature layer. Ideagen Mazlan uses an organization's own QMS data to draft policies, guide investigations, flag compliance gaps ahead of audits and track regulatory changes across jurisdictions in real time. What previously took three days of investigation takes three hours. The platform is purpose-built for GxP and regulated environments and reaches 80%+ adoption on the floor. Most QMS failures trace back to the same causes: quality data fragmented across sites, CAPA processes managed in email chains and documentation that is out of date before it reaches the people who need it. Ideagen Quality Management addresses these directly by centralizing quality workflows and automating document version control and approvals, eliminating the manual overhead that creates compliance risk across sites. Core capabilities include: Non-conformance and CAPA management: capture every non-conformance, guide root cause analysis and track corrective actions through to verified closure so the same issue does not recur Document control: automated versioning, approval workflows and full audit trails ensure every site works from the current, controlled version Audit and inspection management: plan, manage and evidence every audit in one place, with AI-driven monitoring delivering 99%+ reduction in audit findings Supplier quality management: monitor supplier performance, manage non-conformances and coordinate corrective actions across the supply chain Training and competency management: track certifications, qualifications and completion status — new hire training time reduced by 40% Regulatory intelligence: multi-jurisdictional regulatory change monitoring with automated alerts and impact analysis Organizations using the platform report 25-40% improvements in compliance audit scores, 50% faster CAPA cycle times and 30-50% reductions in documentation time. Customers include Nuffield Health, Torbay Pharmaceuticals, Fresenius Kabi, Vector Aerospace and Whyte & Mackay. The platform integrates with ERP, PLM, MES and HR systems and is available in cloud and on-premise deployments. Ideagen Quality Management is well suited to mid-market and enterprise organizations in regulated industries managing quality across multiple sites or standards, where fragmented systems and manual processes create compliance and operational risk.

Average Rating: 4.0/5.0

Total Reviews: 495

How Do G2 Users Rate Ideagen Quality Management?

  • Has the product been a good partner in doing business?: 7.8/10 (Category avg: 9.1/10)
  • Corrective Actions: 7.8/10 (Category avg: 8.8/10)
  • Conformance Records: 8.0/10 (Category avg: 8.9/10)
  • Flexibility: 6.9/10 (Category avg: 8.6/10)

Who Is the Company Behind Ideagen Quality Management?

  • Seller: Ideagen
  • Company Website:
  • Year Founded: 2000
  • HQ Location: Ruddington, Nottingham
  • Twitter: @Ideagen_
    2,172 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    1,386 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Manager, Quality Engineer
  • Top Industries: Hospital & Health Care, Manufacturing
  • Company Size: 55% Medium, 26% Small

What Do G2 Reviewers Say About Ideagen Quality Management?

AI-generated summary from verified user reviews

Pros
  • Users appreciate the ease of use of Ideagen Quality Management, finding it user-friendly for managing QMS activities.
  • Users value the intuitive and comprehensive QMS management that consolidates all activities in one user-friendly platform.
  • Users appreciate the improved customer service of Ideagen Quality Management, contributing to a better overall experience.
  • Users value the organized documentation and automated conformance features of Ideagen Quality Management, enhancing compliance and efficiency.
  • Users value the efficiency of document control in Ideagen Quality Management, streamlining supplier interactions and ensuring compliance.
Cons
  • Users find customer support inadequate, citing slow responses and a lack of competence in resolving issues promptly.
  • Users face difficult usability with Ideagen Quality Management, struggling with bugs and limited reporting capabilities.
  • Users note that the expensive licensing and support costs significantly impact the overall value of Ideagen Quality Management.
  • Users are frustrated with the slow performance of Ideagen Quality Management, causing significant work delays and inefficiencies.
  • Users report experiencing software bugs that cause crashes and technical errors, affecting the workflow and user satisfaction.

What Are Recent G2 Reviews of Ideagen Quality Management?

EASE

EASE is the AI-Powered Audit Management Platform for manufacturers. It's how plants catch, correct, and prevent execution drift, the gap between defined standards and what actually happens on the plant floor. Uncaught, that gap leads to non-conformances: scrap, escapes, customer complaints. Today, nearly 300,000 users across 3,500+ plants in 60 countries complete 6 million+ audits a year, and counting. Quality, EHS, and Operations leaders in automotive, aerospace, food and beverage, consumer goods, and industrial plants use EASE to run the audits that make sure what's supposed to happen actually does: layered process audits (LPAs), safety inspections, Gemba walks, 5S, quality checks. Scheduling and visibility keep programs built around IATF 16949, ISO 9001, AS9100, and ISO 45001 on cadence across shifts, lines, and sites. Most audit software does one job well: documenting what you found. Then the finding sits. Someone chases it. The same problem comes back next quarter on a different shift. EASE is built for what comes after the catch: the failed question becomes a finding with an owner the moment it happens, corrective action and root cause analysis follow, retraining is assigned straight from the finding, and validation confirms the fix held, so what gets found gets fixed, and stays fixed. One system. The whole loop. Day to day, that looks like: - Audit at the line, not at a desk later, with native iOS, Android, and Windows apps, offline included - Build your own audits from a shared question library, and change them yourself as your control plan and PFMEA evolve - Hold the LPA cadence with layer-based scheduling and reminders, so coverage stays visible, missed audits drop, and on-time completion climbs - Close every finding with owned corrective actions, root cause analysis, validation, and retraining assigned straight from the finding, AI-drafted from your own SOPs - Track leading indicators on real-time dashboards, with AI-summarized reports that flag patterns by auditor and location and recommend where to act - Drive adoption at scale: unlimited users at every tier, no email needed to log in, and AI translation across 29 languages, so the whole floor is in the system, not just the quality desk Turning audits into continuous improvement means big results. Dana cut internal defect PPM by 47%. Eaton cut customer escapes in half. One Tier 1 automotive supplier climbed from 40% to 91% audit completion after leaving a legacy LPA tool behind. And between audits, EASE IQ's AI camera vision monitors plant-floor conditions and routes what it detects into the same findings and corrective action workflows. The loop runs even when nobody is walking the line. With EASE, you get visibility. Visibility drives accountability. Accountability builds operational discipline. That is what EASE delivers.

Average Rating: 4.6/5.0

Total Reviews: 232

How Do G2 Users Rate EASE?

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

Who Is the Company Behind EASE?

  • Seller: Ease.io
  • Company Website:
  • Year Founded: 1986
  • HQ Location: Irvine, California
  • Twitter: @easeaudits
    1,043 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    89 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Manager, Quality Engineer
  • Top Industries: Automotive, Manufacturing
  • Company Size: 61% Medium, 25% Large

What Do G2 Reviewers Say About EASE?

AI-generated summary from verified user reviews

Pros
  • Users find the ease of use in EASE exceptional, allowing for effortless scheduling and customization for their business needs.
  • Users find EASE to be easy to use, enjoying its intuitive design and efficient audit capabilities.
  • Users value the ease of creating and tracking audits, highlighting its straightforward implementation and user-friendly design.
  • Users find EASE to be intuitive and user-friendly, making it easy to document issues and customize features.
  • Users commend the ease of auditing with EASE, simplifying the process and enhancing customization for business needs.
Cons
  • Users find the inefficiency in workflows and report generation to be a significant drawback of EASE.
  • Users find the limited customization options in EASE restrict their experience and hinder overall efficiency.
  • Users find the limited options for workflow customization hinder efficient processes and complicate user experience.
  • Users find EASE not user-friendly, citing difficulties with login and confusing design features that hinder its usability.
  • Users experience inadequate reporting in EASE, finding it time-consuming and missing essential notes for audits.

What Are Recent G2 Reviews of EASE?

MasterControl Quality Management System

MasterControl Quality Excellence (Qx) is the #1 Quality Management System (QMS) in life sciences. Built on an AI-driven platform, it enables life-sciences companies to enable flexible quality event management, simplified document management, and automated training management—that all work seamlessly together to close the loop on quality. Qx is trusted by more than 1,300 pharmaceutical, biotech, and medical device companies. Qx is an electronic quality management system (eQMS) purpose-built for regulated manufacturers that must comply with FDA 21 CFR Part 11, EU GMP Annex 11, ISO 13485, GxP, and other global quality requirements, including EMA, MHRA, Health Canada, TGA, and PMDA jurisdictions. Qx connects document control, change control, training, quality event management (including CAPA), audits, and risk in a single closed-loop system, so information moves automatically between processes instead of through manual handoffs. When a document changes, training assignments trigger automatically. When a quality event opens, related CAPAs launch with context already populated. Every action generates an immutable, audit-ready record — so instead of assembling evidence before an inspection, teams retrieve it in seconds. Qx's patented Validation Excellence Tool (VxT) and Validation on Demand (VoD) reduce computer system validation from a months-long project to a process measured in minutes, aligned with FDA Computer Software Assurance (CSA) guidance — more than 90% of VxT customers perform no additional formal testing. Compliant, purpose-built AI tools accelerate document review, exam creation, and quality event summarization while keeping humans in control. Used by pharmaceutical, biotech, and medical device manufacturers across North America, Europe, Asia-Pacific, and other global regulated markets, Qx scales from single-site startups to global, multi-site enterprises on one validated platform — no re-platforming required as organizations grow. Natively connected to MasterControl Manufacturing Excellence (Mx) and Asset Excellence (Ax), Qx extends quality directly to the shop floor and into asset management, creating one source of truth across the entire regulated operation.

Average Rating: 4.3/5.0

Total Reviews: 526

How Do G2 Users Rate MasterControl Quality Management System?

  • Has the product been a good partner in doing business?: 8.8/10 (Category avg: 9.1/10)
  • Corrective Actions: 7.5/10 (Category avg: 8.8/10)
  • Conformance Records: 7.6/10 (Category avg: 8.9/10)
  • Flexibility: 7.6/10 (Category avg: 8.6/10)

Who Is the Company Behind MasterControl Quality Management System?

  • Seller: MasterControl
  • Company Website:
  • Year Founded: 1993
  • HQ Location: Salt Lake City, UT
  • Twitter: @MCMasterControl
    6,258 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    690 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Assurance Specialist, Quality Engineer
  • Top Industries: Pharmaceuticals, Medical Devices
  • Company Size: 64% Medium, 25% Large

What Do G2 Reviewers Say About MasterControl Quality Management System?

AI-generated summary from verified user reviews

Pros
  • Users highlight the user-friendly interface of MasterControl, which simplifies quality management and enhances operational efficiency.
  • Users appreciate the centralized document management of MasterControl, enhancing collaboration and streamlining compliance processes.
  • Users appreciate the user-friendly training system that integrates seamlessly with other quality management functions.
  • Users value the integration and efficiency of MasterControl's document control, enhancing compliance and process management.
  • Users value the consistency and ease of use of MasterControl, enhancing efficiency and adaptability for teams.
Cons
  • Users find MasterControl's interface not intuitive, as it can be complicated and intimidating for new users.
  • Users find a learning curve with MasterControl, requiring time to acclimate and fully utilize the system's features.
  • Users find difficult usability in MasterControl's Quality Management System, struggling with report creation and navigation.
  • Users find the MasterControl interface not user-friendly, especially for newcomers struggling with its complexity.
  • Users find the complex setup of MasterControl can lead to manual updates and training gaps for trainees.

What Are Recent G2 Reviews of MasterControl Quality Management System?

What Are G2 Users Discussing About MasterControl Quality Management System?

Propel

Propel helps product companies grow revenue and increase business value with a unified platform that delivers PLM, QMS, PIM, and supplier management capabilities—all powered by embedded AI. Our solution connects commercial and product teams with a single, continuous product thread that accelerates decision-making, drives process efficiencies, and empowers teams to deliver compelling products and experiences across all customer touchpoints. Product Lifecycle Management (PLM): Propel PLM delivers practical, embedded AI that enhances everyday product and quality workflows with real-world use cases—accelerating change reviews, summarizing complex product records, identifying BOM and quality risks, and guiding users with context-aware insights. Built for modern enterprises, our PLM supports complex product structures, global teams, and regulated environments without sacrificing usability. Quality Management System (QMS): Propel QMS is a complete, enterprise-grade standalone solution that can be deployed independently with all core modules included out-of-the-box—CAPA, Complaints, NCMR, Audits, Deviations, Training, Equipment Calibration, and Supplier Quality. Purpose-built for medical device manufacturers, our cloud-native eQMS reduces validation burden with comprehensive documentation packages (FDA 21 CFR Part 820 & Part 11, ISO 13485:2016, EU MDR) and delivers measurable results including 100% audit pass rates and 8-week rapid deployment. Product Information Management (PIM): Propel PIM is a purpose-built solution that centralizes product data, attributes, and digital assets into a single, trusted system of record—designed to support complex product catalogs and fast-moving go-to-market teams. With Propel One AI embedded directly into the platform, PIM becomes an intelligent, automated system that enriches product information, identifies missing or inconsistent attributes, and summarizes complex product data using trusted, governed sources—accelerating content readiness and maintaining consistency across channels while requiring no dependencies on PLM, ERP, or commerce platforms. Supplier Community: Propel's Supplier Community enables secure, authenticated user access for external suppliers with role-based permissions that protect IP while enabling efficient collaboration on parts, BOMs, quality records, and projects. Launch faster by directly connecting suppliers to internal engineering, quality, and operations teams in a shared workspace, eliminating handoff delays and reducing miscommunication—all without requiring Salesforce. Propel has a proven track record of improving product quality, accelerating time to revenue, and increasing customer satisfaction. Recognized multiple times as a Deloitte Technology Fast 500 winner, Propel drives product success for hyper-growth startups, corporate pioneers, and Fortune 500 leaders in the high-tech, medtech, and consumer goods industries.

Average Rating: 4.3/5.0

Total Reviews: 143

How Do G2 Users Rate Propel?

  • Has the product been a good partner in doing business?: 9.2/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.4/10 (Category avg: 8.8/10)
  • Conformance Records: 8.3/10 (Category avg: 8.9/10)
  • Flexibility: 8.0/10 (Category avg: 8.6/10)

Who Is the Company Behind Propel?

  • Seller: Propel
  • Company Website:
  • Year Founded: 2015
  • HQ Location: Redwood City, CA
  • Twitter: @PropelConverged
    785 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    132 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Medical Devices, Electrical/Electronic Manufacturing
  • Company Size: 49% Medium, 42% Small

What Do G2 Reviewers Say About Propel?

AI-generated summary from verified user reviews

Pros
  • Users find Propel's ease of use enhances team collaboration and simplifies daily project management tasks.
  • Users appreciate the cloud functionality and intuitive integration of Propel, enhancing collaboration and project management efficiency.
  • Users value the seamless collaboration in Propel, simplifying task management and enhancing client engagement effortlessly.
  • Users value the seamless data management of Propel, simplifying access and integration with essential tools effectively.
  • Users highlight the increased efficiency Propel provides, significantly enhancing design and development processes within their organizations.
Cons
  • Users experience slow performance during searches and data processing, which can disrupt their workflow at times.
  • Users find the time-consuming processes of making updates to Propel frustrating and unnecessarily complicated.
  • Users find the learning curve steep, requiring significant time and training for those unfamiliar with Salesforce.
  • Users find the time-consuming procedures and multiple steps for simple updates in Propel quite frustrating.
  • Users experience time delays when loading complex diagrams and during the initial setup, affecting efficiency.

What Are Recent G2 Reviews of Propel?

1factory

1factory's Quality Control and Quality Management software solutions digitize, simplify and automate all Quality Control and Quality Management activities, including, Document Control, Training Management, Quality Planning, Inspection, SPC, PPAP, Gage Calibration, NCR, CAPA and more. With 1factory, manufacturers speed-up QC tasks, improve factory yield, maintain compliance, and ace their audits.

Average Rating: 5.0/5.0

Total Reviews: 21

How Do G2 Users Rate 1factory?

  • Has the product been a good partner in doing business?: 10.0/10 (Category avg: 9.1/10)
  • Corrective Actions: 7.2/10 (Category avg: 8.8/10)
  • Conformance Records: 7.5/10 (Category avg: 8.9/10)
  • Flexibility: 9.4/10 (Category avg: 8.6/10)

Who Is the Company Behind 1factory?

  • Seller: 1factory
  • Year Founded: 2011
  • HQ Location: Milpitas, CA
  • Twitter: @1FactoryInc
    130 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    20 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Machinery
  • Company Size: 62% Small, 33% Medium

What Do G2 Reviewers Say About 1factory?

AI-generated summary from verified user reviews

Pros
  • Users praise the ease of use of 1factory, finding the software simple and intuitive for quick implementation.
  • Users value the all-in-one functionality of 1factory, enhancing efficiency with dynamic features and excellent support.
  • Users love the intuitive UI of 1factory, making it easy to learn and implement quickly.
  • Users praise the responsive customer support of 1factory, finding it helpful and efficient for their needs.
  • Users find 1factory's easy learning curve and intuitive UI greatly enhance productivity and efficiency for quality departments.
Cons
  • Users face a confusing interface in 1factory, struggling with navigation and advanced features' learning curve.
  • Users find it difficult to modify old prints due to clunky processes related to attached inspection reports.
  • Users find it difficult to modify old prints due to clunky processes tied to inspection report history.
  • Users find that editing old prints can be clunky, especially when inspection reports are linked to them.
  • Users find the steep learning curve of 1Factory for advanced features challenging and navigation can be difficult.

What Are Recent G2 Reviews of 1factory?

What Are G2 Users Discussing About 1factory?

ZenQMS

ZenQMS was founded in 2009 by Life Sciences & quality management veterans with firsthand knowledge of the frustrations and dangers that come with using manual or home-grown systems to manage GxP compliance. As a result, we built software that's easier to use, designed for scale, and geared specifically for the complex and changing needs of Life Sciences companies, large and small. ZenQMS' approach to client engagement is a true outlier, particularly in terms of our pricing model and approach to support / implementation. Our annual fee schedule is totally transparent; it eliminates restrictive seat licenses and a la carte upselling in favor of providing access to ALL MODULES and services for ALL USERS from Day 1. These include connected modules for document control, training, issues, change control, and audits, as well as lifetime in-house support at no additional cost. You don't need an IT team or large QA team to purchase, implement, or manage ZenQMS. We do the heavy lifting with you. ZenQMS meets all 21 CFR Part 11/ Annex 11 and relevant GxP/ ISO requirements for small- and large-scale Life Sciences industries including: Biotech, pharmaceutical companies, CROs, CDMOs, Labs, Packaging and Logistics companies, and GxP Software developers, Commercial ventures/Spin-outs, and Consumer Products organizations. We have hundreds of clients with users in over 100 countries that span pre-clinical to commercial scale. Call us. We can help.

Average Rating: 4.7/5.0

Total Reviews: 127

How Do G2 Users Rate ZenQMS?

  • Has the product been a good partner in doing business?: 9.4/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.4/10 (Category avg: 8.8/10)
  • Conformance Records: 9.1/10 (Category avg: 8.9/10)
  • Flexibility: 9.0/10 (Category avg: 8.6/10)

Who Is the Company Behind ZenQMS?

  • Seller: ZenQMS
  • Company Website:
  • Year Founded: 2010
  • HQ Location: Ardmore, Pennsylvania
  • Twitter: @ZenQMS
    122 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    99 employees on LinkedIn®

Who Uses This Product?

  • Who Uses This: Quality Assurance Manager
  • Top Industries: Pharmaceuticals, Biotechnology
  • Company Size: 49% Medium, 38% Small

What Do G2 Reviewers Say About ZenQMS?

AI-generated summary from verified user reviews

Pros
  • Users commend the ease of use of ZenQMS, finding it intuitive and simple to implement across their organization.
  • Users commend ZenQMS for its responsive and knowledgeable customer support, enhancing confidence in compliance and usability.
  • Users praise the easy implementation of ZenQMS, allowing quick and smooth transitions from traditional systems.
  • Users value the flexibility and configurability of ZenQMS, allowing easy customization to suit specific organizational needs.
  • Users value the clear and organized design of ZenQMS, enhancing their daily Quality Assurance efforts seamlessly.
Cons
  • Users find access restrictions challenging, with difficulties in password recovery and frequent automatic logouts.
  • Users face formatting issues in ZenQMS, particularly with exported reports and online forms in PDFs.
  • Users find the learning curve steep for ZenQMS, needing time to become comfortable with its features.
  • Users find the documents module problematic due to slow support and issues with search and presentation of archived documents.
  • Users find ZenQMS to be not intuitive, struggling with document numbering and a cumbersome signature workflow.

What Are Recent G2 Reviews of ZenQMS?

What Are G2 Users Discussing About ZenQMS?

SAP ECC

Leverage world-class ERP software. Sharpen your competitive edge and drive growth with enterprise resource planning from SAP. With more than 40 years of experience and nearly 50,000 customers, our market-leading enterprise resource planning (ERP) software is a proven, trusted foundation built to support the world۪s largest organizations as well as small and midsize companies in 25 different industries. Leverage role-based access to critical data, applications, and analytical tools and streamline your processes across procurement, manufacturing, service, sales, finance, and HR.

Average Rating: 4.2/5.0

Total Reviews: 864

How Do G2 Users Rate SAP ECC?

  • Has the product been a good partner in doing business?: 8.0/10 (Category avg: 9.1/10)
  • Corrective Actions: 8.8/10 (Category avg: 8.8/10)
  • Conformance Records: 8.4/10 (Category avg: 8.9/10)
  • Flexibility: 8.0/10 (Category avg: 8.6/10)

Who Is the Company Behind SAP ECC?

  • Seller: SAP
  • Year Founded: 1972
  • HQ Location: Walldorf
  • Twitter: @SAP
    297,052 Twitter followers
  • LinkedIn® Page: www.linkedin.com
    149,349 employees on LinkedIn®
  • Ownership: NYSE:SAP

Who Uses This Product?

  • Who Uses This: Consultant, Assistant Manager
  • Top Industries: Information Technology and Services, Accounting
  • Company Size: 64% Large, 29% Medium

What Do G2 Reviewers Say About SAP ECC?

AI-generated summary from verified user reviews

Pros
  • Users value the seamless departmental integration of SAP ECC, enhancing operations and simplifying data management across functions.
  • Users find SAP ECC to be easy to use, thanks to its intuitive transaction code interface and detailed data entry.
  • Users value the seamless integration of SAP ECC, which enhances collaboration and streamlines various business functions effectively.
  • Users value the seamless integration across departments in SAP ECC, enhancing operational efficiency and data flow.
  • Users appreciate the strong integration features of SAP ECC, ensuring smooth data flow across departments for streamlined operations.
Cons
  • Users find the time-consuming implementation process of SAP ECC a significant burden, affecting overall efficiency and usability.
  • Users find the complex setup of SAP ECC frustrating, requiring extensive time and resources for effective implementation.
  • Users criticize the steep learning curve of SAP ECC, citing its complex interface and cumbersome processes as major drawbacks.
  • Users find SAP ECC not user-friendly, citing its steep learning curve and outdated interface as major drawbacks.
  • Users find SAP ECC user-unfriendly due to its complex interface, requiring extensive training and skilled resources.

What Are Recent G2 Reviews of SAP ECC?

What Are G2 Users Discussing About SAP ECC?

CertCrowd

CertCrowd is a SAAS solution for ISO Compliance and GRC. Manage your compliance to ISO standards simply and easily with CertCrowd with powerful GRC (governance, risk and compliance) tools such as risk management, incident management and corrective action, frameworks, manual, actions and reports; CertCrowd makes ISO systems for ISO9001 Quality, ISO27001 Information Security, ISO42001 Ai Management, ISO14001 Environment, ISO45001 Safety, ISO13485 Medical Devices simple, easy and affordable

Average Rating: 4.9/5.0

Total Reviews: 19

How Do G2 Users Rate CertCrowd?

  • Has the product been a good partner in doing business?: 9.7/10 (Category avg: 9.1/10)
  • Corrective Actions: 9.4/10 (Category avg: 8.8/10)
  • Conformance Records: 9.8/10 (Category avg: 8.9/10)
  • Flexibility: 8.8/10 (Category avg: 8.6/10)

Who Is the Company Behind CertCrowd?

  • Seller: Certcrowd
  • Company Website:
  • Year Founded: 2019
  • HQ Location: Brisbane, AU
  • LinkedIn® Page: www.linkedin.com
    4 employees on LinkedIn®

Who Uses This Product?

  • Top Industries: Consulting
  • Company Size: 84% Small, 11% Medium

What Do G2 Reviewers Say About CertCrowd?

AI-generated summary from verified user reviews

Pros
  • Users commend the ease of use of CertCrowd, simplifying compliance management and enhancing operational efficiency.
  • Users value the simple and structured compliance process provided by CertCrowd, enhancing manageability and audit success.
  • Users appreciate how CertCrowd simplifies compliance management, making processes easier and audits more successful.
  • Users appreciate the effective evidence management of CertCrowd, facilitating seamless compliance and streamlined audit processes.
  • Users appreciate the ease of use and configurability of CertCrowd, making it an ideal choice for GRC solutions.
Cons
  • Users experience a steep learning curve with CertCrowd, needing time to navigate and optimize the platform effectively.
  • Users find the user interface complicated, though they acknowledge the powerful template management system compensates for it.
  • Users report encountering annoying bugs that require refreshing, though issues are typically resolved quickly by support.
  • Users face a confusing interface in CertCrowd, leading to a steep learning curve for effective navigation.
  • Users face a difficult initiation with CertCrowd, requiring time to learn and efficiently navigate the software.

What Are Recent G2 Reviews of CertCrowd?

Daniel Rivera
DR
Researched and written by Daniel Rivera
Updated