# Best Medical Quality Management Systems (QMS) ## How Many Medical Quality Management Systems (QMS) Products Does G2 Track? **Total Products under this Category:** 121 ### Category Stats (Aug 2026) - **Average Rating:** 4.39/5 (↑0.01 vs Jul 2026) The average rating of products in this category, based on all submitted ratings - **Top Trending Product:** ValGenesis Validation Lifecycle Suite (+1.2%) - Among all products in this category, ValGenesis Validation Lifecycle Suite recorded the largest rating increase compared to last month _Last updated: August 06, 2026_ ## How Does G2 Rank Medical Quality Management Systems (QMS) Products? **Why You Can Trust G2's Software Rankings:** - 30 Analysts and Data Experts - 4,700+ Authentic Reviews - 121+ 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 Medical Quality Management Systems (QMS) ![G2 Grid® for Medical Quality Management Systems (QMS) plotting products by satisfaction and market presence](https://www.g2.com/categories/medical-qms/grids.png?focus%5B%5D=4169&focus%5B%5D=142801&focus%5B%5D=17363&focus%5B%5D=80861&focus%5B%5D=1470&focus%5B%5D=1255729&focus%5B%5D=39899&focus%5B%5D=50982) Highlighted products: Qualio, Kneat Gx, TrackWise, Grand Avenue Software, Arena PLM & QMS, SimplerQMS, Octave Reliance (ETQ Reliance), and QT9 QMS. Underlying data: [Grid® JSON](https://www.g2.com/categories/medical-qms/grids.json?focus%5B%5D=qualio&focus%5B%5D=kneat-gx&focus%5B%5D=honeywell-trackwise&focus%5B%5D=grand-avenue-software&focus%5B%5D=arena-plm-qms&focus%5B%5D=simplerqms&focus%5B%5D=octave-reliance-etq-reliance&focus%5B%5D=qt9-qms) **Sponsored** ### Grand Avenue Software Grand Avenue Software (GAS) is a specialized quality management system (QMS) solution designed to assist life science companies in streamlining their operations and fostering innovation. This software addresses the complexities associated with documentation, compliance, and audit processes, enabling teams to shift their focus from managing administrative tasks to developing superior products. In a highly regulated industry where quality control is paramount, GAS serves as a critical tool for enhancing operational efficiency. The primary target audience for GAS includes life science organizations, such as pharmaceutical and biotechnology firms, that require robust quality management solutions to navigate the intricacies of regulatory compliance. These companies often grapple with challenges like documentation chaos and compliance friction, which can impede their ability to innovate and respond to market demands. GAS offers a modular approach, allowing organizations to implement specific features tailored to their immediate needs while maintaining the flexibility to scale as their requirements evolve. This adaptability is essential for companies operating in a dynamic and fast-paced environment. One of the key features of GAS is its configurable templates, which facilitate rapid onboarding and help organizations achieve regulatory readiness more efficiently. This feature not only accelerates the time to value for users but also ensures predictable pricing, making it easier for companies to budget for their quality management needs. Additionally, GAS provides hands-on implementation and ongoing guidance tailored to each customer’s unique processes. This personalized support ensures that organizations can maximize the benefits of the system, ultimately leading to improved operational outcomes. Moreover, GAS distinguishes itself through its two decades of experience in supporting life science quality teams. This extensive background positions the company as a stable and reliable partner for organizations looking to enhance their quality management practices. By reducing audit risk and simplifying compliance processes, GAS empowers life science companies to prioritize innovation and product development. This focus on quality not only helps organizations meet regulatory standards but also contributes to their long-term success in a competitive marketplace, allowing them to thrive while maintaining the highest levels of quality assurance. [Visit website](https://www.g2.com/external_clickthroughs/record?secure%5Bad_program%5D=ppc&secure%5Bad_slot%5D=category_product_list_llm&secure%5Bcategory_id%5D=1884&secure%5Bchosen_at%5D=2026-08-09T10%3A38%3A33Z&secure%5Bdisplayable_resource_id%5D=1884&secure%5Bdisplayable_resource_type%5D=Category&secure%5Bmedium%5D=sponsored&secure%5Bplacement_reason%5D=page_category&secure%5Bplacement_resource_ids%5D%5B%5D=1884&secure%5Bprioritized%5D=false&secure%5Bproduct_id%5D=80861&secure%5Bresource_id%5D=1884&secure%5Bresource_type%5D=Category&secure%5Bsource_type%5D=category_page&secure%5Bsource_url%5D=https%3A%2F%2Fwww.g2.com%2Fcategories%2Fmedical-qms%3Fopen_modal_url%3D%252Fproducts%252Falmond%252Fwishlists%253Fhost_path%253D%25252Fcategories%25252Fmedical-qms%2526source%253Dcategory&secure%5Btoken%5D=e2a323aa48c945441685fa7f57371452d1f71b9bc6853b8073abddbd03964e7a&secure%5Burl%5D=https%3A%2F%2Fgrandavenue.com%2Fget-a-demo%2F%3Futm_source%3Dg2%26utm_medium%3Dlead_aggregator%26utm_campaign%3Dcpc&secure%5Burl_type%5D=custom_url) ### [Qualio](https://www.g2.com/products/qualio/reviews) 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) - **Design Controls:** 8.1/10 (Category avg: 8.5/10) - **Quality Processes:** 8.9/10 (Category avg: 9.0/10) - **Audit Management:** 8.5/10 (Category avg: 8.6/10) #### Who Is the Company Behind Qualio? - **Seller:** [Qualio](https://www.g2.com/sellers/qualio) - **Company Website:** www.qualio.com - **Year Founded:** 2012 - **HQ Location:** San Francisco, California - **Twitter:** @qualiohq 711 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=3fd10a9fa4c3102febd247de60e18c839b14ee7fced992dc9ccce7c05e946ceb&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F2498463%2F&secure%5Burl_type%5D=linkedin_company_website) 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 commend Qualio for its **ease of use** , simplifying training and increasing efficiency with a clean interface. - Users love Qualio’s **user-friendly training modules** , which enhance efficiency and simplify tracking for all employees. - Users appreciate the **extremely searchable document management** in Qualio, streamlining control, storage, and approval processes. - Users value the **audit trail feature** in Qualio, ensuring clear tracking of document reviews and approvals. - Users praise Qualio for its **intuitive interface** , making quality management easy and efficient for everyone. ##### Cons - Users find **document management cumbersome** in Qualio, facing long setup times and frustrating editing issues. - Users find **feature limitations** in Qualio, particularly with slow performance, lack of theme options, and integration challenges. - Users find **difficult usability** in Qualio, facing challenges with document editing and formatting inconsistencies. - Users find the **user interface of Qualio frustrating** due to cumbersome text editing and lack of version control. - Users face **editing difficulties** with table formatting and lack timely notifications for overdue document reviews in Qualio. #### What Are Recent G2 Reviews of Qualio? **["Helpful QMS Platform for Daily Operations"](https://www.g2.com/survey_responses/qualio-review-9942483)** **Rating:** 4.5/5.0 stars _— Divyanshu R._ [Read full review](https://www.g2.com/survey_responses/qualio-review-9942483) **["It makes my onboarding life easier"](https://www.g2.com/survey_responses/qualio-review-12926290)** **Rating:** 4.5/5.0 stars _— Marta G._ [Read full review](https://www.g2.com/survey_responses/qualio-review-12926290) #### What Are G2 Users Discussing About Qualio? - [What is Qualio used for?](https://www.g2.com/discussions/what-is-qualio-used-for) - 1 comment, 1 upvote - [What does Qualio do?](https://www.g2.com/discussions/what-does-qualio-do) - 6 comments, 5 upvotes - [What is Eqms quality management system?](https://www.g2.com/discussions/what-is-eqms-quality-management-system) - 2 comments, 1 upvote - [What is QMS software?](https://www.g2.com/discussions/what-is-qms-software) - 2 comments, 1 upvote - [What is Qualio?](https://www.g2.com/discussions/what-is-qualio) - 3 comments, 2 upvotes ### [Kneat Gx](https://www.g2.com/products/kneat-gx/reviews) Kneat Gx is the only digital validation platform proven to deliver any validation process in one platform, your way, with unparalleled data integrity and usability. Now enhanced with Kneat AI, it is an end-to-end digital validation management platform enabling regulated companies to make validation easier, faster, and smarter than ever before. Why Leading Life Sciences Choose Kneat Our purpose-built software streamlines the validation lifecycle for BioPharma and Medical Device companies. By integrating advanced AI capabilities, Kneat Gx empowers users to automate repetitive tasks, gain deeper insights from their data, and accelerate speed-to-market. • Compliant & Secure: Fully 21 CFR Part 11 and EudraLex Annex 11 compliant. • Intelligence-Driven: Leverages AI to optimize document creation, manage complex workflows, and proactively identify compliance gaps. • Data Sovereignty: Eliminates paper-based silos, providing an unprecedented capability to create, manage, and mine validation data in real-time. • Industry Trusted: Trusted by the leaders in Life Sciences—including eight of the top 10 global companies—where equipment, computer systems, and processes must meet the highest standards for product quality and patient safety. The Kneat Advantage: By combining the flexibility of our enterprise platform with the power of AI, we transform validation from a regulatory burden into a strategic advantage. **Average Rating:** 4.5/5.0 **Total Reviews:** 96 #### How Do G2 Users Rate Kneat Gx? - **Has the product been a good partner in doing business?:** 9.6/10 (Category avg: 9.1/10) - **Design Controls:** 8.9/10 (Category avg: 8.5/10) - **Quality Processes:** 10.0/10 (Category avg: 9.0/10) - **Audit Management:** 9.2/10 (Category avg: 8.6/10) #### Who Is the Company Behind Kneat Gx? - **Seller:** [Kneat Solutions](https://www.g2.com/sellers/kneat-solutions) - **Company Website:** kneat.com - **Year Founded:** 2006 - **HQ Location:** Limerick, IE - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=c151dd4466743c96b88614eaf9278e908f1579991140cc8eff64bf763c6c6214&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fkneat-solutions-ltd&secure%5Burl_type%5D=linkedin_company_website) 342 employees on LinkedIn® - **Ownership:** FRA: FOBK #### Who Uses This Product? - **Top Industries:** Pharmaceuticals, Biotechnology - **Company Size:** 43% Large, 42% Medium #### What Do G2 Reviewers Say About Kneat Gx? _AI-generated summary from verified user reviews_ ##### Pros - Users appreciate the **ease of use** of Kneat Gx, simplifying reviews, approvals, and ensuring compliance and transparency. - Users appreciate the **user-friendly design** of Kneat Gx, which centralizes features and promotes a paperless validation process. - Users value the **efficiency improvement** provided by Kneat Gx, streamlining validation processes into a digital format. - Users value the **tracking efficiency** of Kneat Gx, facilitating compliance and enhancing the validation document management process. - Users value the **flexibility and centralized access** of Kneat Gx, enabling efficient document management and traceability. ##### Cons - Users experience **feature limitations** with Kneat Gx, disrupting workflows and restricting options without vendor support. - Users experience a **steep learning curve** , making it challenging to adapt to Kneat Gx effectively. - Users face a **noticeable learning curve** , making it time-consuming to fully grasp and adapt to Kneat Gx. - Users report **slow performance** with Kneat Gx, experiencing lag and glitches during important document workflows. - Users report **software bugs** in Kneat Gx, leading to slow loading and disruptions during document workflows. #### What Are Recent G2 Reviews of Kneat Gx? **["Will transform your traditional validation program and processes"](https://www.g2.com/survey_responses/kneat-gx-review-10955323)** **Rating:** 5.0/5.0 stars _— Kathianne R._ [Read full review](https://www.g2.com/survey_responses/kneat-gx-review-10955323) **["Highly Configurable Platform with a Smooth, Streamlined Implementation"](https://www.g2.com/survey_responses/kneat-gx-review-12528209)** **Rating:** 5.0/5.0 stars _— Nico V._ [Read full review](https://www.g2.com/survey_responses/kneat-gx-review-12528209) ### [TrackWise](https://www.g2.com/products/honeywell-trackwise/reviews) TrackWise® is the world’s leading on-premises QMS software. It brings all your quality processes together in a single place to give you the big picture of your compliance and operational effectiveness. TrackWise offers several industry best-practice workflows and can also adapt to fit your existing process and workflow. Companies across several industries use TrackWise to increase efficiency, improve quality, achieve compliance and reduce risk. **Average Rating:** 4.3/5.0 **Total Reviews:** 48 #### How Do G2 Users Rate TrackWise? - **Has the product been a good partner in doing business?:** 7.9/10 (Category avg: 9.1/10) - **Design Controls:** 9.2/10 (Category avg: 8.5/10) - **Quality Processes:** 8.3/10 (Category avg: 9.0/10) - **Audit Management:** 8.3/10 (Category avg: 8.6/10) #### Who Is the Company Behind TrackWise? - **Seller:** [Honeywell Technologies](https://www.g2.com/sellers/honeywell-technologies) - **Year Founded:** 1906 - **HQ Location:** Charlotte, North Carolina - **Twitter:** @HoneywellNow 2,526 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=2439934c193c64f590ac3e59168d5255fa5931a7d9141987b03ad28a37fa5cfe&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fhoneywell%2F&secure%5Burl_type%5D=linkedin_company_website) 132,085 employees on LinkedIn® - **Ownership:** HON #### Who Uses This Product? - **Top Industries:** Pharmaceuticals, Biotechnology - **Company Size:** 56% Large, 35% Medium #### What Do G2 Reviewers Say About TrackWise? _AI-generated summary from verified user reviews_ ##### Pros - Users find TrackWise to be **very easy to use** , appreciating its flexibility and customization options for workflows. - Users enjoy the **ease of use and customization** of TrackWise, enhancing flexibility for various workflows and needs. - Users value the **great flexibility and ease of use** in customizing workflows and metadata fields on TrackWise. - Users value the **robust automation** capabilities of TrackWise, enhancing their workflow efficiency significantly. - Users appreciate the **great flexibility** of TrackWise, enabling extensive customization of metadata fields and workflows. ##### Cons - Users express frustration over **inefficient notifications** causing loss of unsaved work when timeouts occur. - Users express dissatisfaction with **poor collaboration** due to inadequate customer support and lack of community networking opportunities. - Users are frustrated by the **poor customer support** and absence of a networking community for sharing experiences. - Users are frustrated by the **time consumption** of TrackWise, often losing work due to timeouts before saving. - Users often face **time-consumption issues** with TrackWise, as losing unsaved work due to timeouts can be frustrating. #### What Are Recent G2 Reviews of TrackWise? **["Trackwise good for tracking all QMS record and user friendly.All QMS records available in excelsheet"](https://www.g2.com/survey_responses/trackwise-review-7442437)** **Rating:** 5.0/5.0 stars _— Ravindra J._ [Read full review](https://www.g2.com/survey_responses/trackwise-review-7442437) **["Very Easy to Use, Feature-Rich, and Highly Flexible Customization"](https://www.g2.com/survey_responses/trackwise-review-12250052)** **Rating:** 4.0/5.0 stars _— Marco B._ [Read full review](https://www.g2.com/survey_responses/trackwise-review-12250052) #### What Are G2 Users Discussing About TrackWise? - [How do you use Track wise?](https://www.g2.com/discussions/how-do-you-use-track-wise) - [Is TrackWise built on Salesforce?](https://www.g2.com/discussions/is-trackwise-built-on-salesforce) - [What is a TrackWise module?](https://www.g2.com/discussions/what-is-a-trackwise-module) - [What is TrackWise software used for?](https://www.g2.com/discussions/what-is-trackwise-software-used-for) ### [Grand Avenue Software](https://www.g2.com/products/grand-avenue-software/reviews) Grand Avenue Software (GAS) is a specialized quality management system (QMS) solution designed to assist life science companies in streamlining their operations and fostering innovation. This software addresses the complexities associated with documentation, compliance, and audit processes, enabling teams to shift their focus from managing administrative tasks to developing superior products. In a highly regulated industry where quality control is paramount, GAS serves as a critical tool for enhancing operational efficiency. The primary target audience for GAS includes life science organizations, such as pharmaceutical and biotechnology firms, that require robust quality management solutions to navigate the intricacies of regulatory compliance. These companies often grapple with challenges like documentation chaos and compliance friction, which can impede their ability to innovate and respond to market demands. GAS offers a modular approach, allowing organizations to implement specific features tailored to their immediate needs while maintaining the flexibility to scale as their requirements evolve. This adaptability is essential for companies operating in a dynamic and fast-paced environment. One of the key features of GAS is its configurable templates, which facilitate rapid onboarding and help organizations achieve regulatory readiness more efficiently. This feature not only accelerates the time to value for users but also ensures predictable pricing, making it easier for companies to budget for their quality management needs. Additionally, GAS provides hands-on implementation and ongoing guidance tailored to each customer’s unique processes. This personalized support ensures that organizations can maximize the benefits of the system, ultimately leading to improved operational outcomes. Moreover, GAS distinguishes itself through its two decades of experience in supporting life science quality teams. This extensive background positions the company as a stable and reliable partner for organizations looking to enhance their quality management practices. By reducing audit risk and simplifying compliance processes, GAS empowers life science companies to prioritize innovation and product development. This focus on quality not only helps organizations meet regulatory standards but also contributes to their long-term success in a competitive marketplace, allowing them to thrive while maintaining the highest levels of quality assurance. **Average Rating:** 5.0/5.0 **Total Reviews:** 12 #### How Do G2 Users Rate Grand Avenue Software? - **Has the product been a good partner in doing business?:** 9.7/10 (Category avg: 9.1/10) - **Design Controls:** 10.0/10 (Category avg: 8.5/10) - **Quality Processes:** 10.0/10 (Category avg: 9.0/10) - **Audit Management:** 10.0/10 (Category avg: 8.6/10) #### Who Is the Company Behind Grand Avenue Software? - **Seller:** [Grandavenue](https://www.g2.com/sellers/grandavenue) - **Company Website:** grandavenue.com - **Year Founded:** 2002 - **HQ Location:** Saint Paul, US - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=99fdee4c56b346aae13d95405cb7690ff540b52f8a274460830a6aaf8086cc77&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fgrand-avenue-software%2F&secure%5Burl_type%5D=linkedin_company_website) 26 employees on LinkedIn® #### Who Uses This Product? - **Top Industries:** Medical Devices - **Company Size:** 50% Small, 50% Medium #### What Are Recent G2 Reviews of Grand Avenue Software? **["Affordable, Easy-to-Use eQMS That Streamlines Compliance and Workflows"](https://www.g2.com/survey_responses/grand-avenue-software-review-13171047)** **Rating:** 5.0/5.0 stars _— Tom R._ [Read full review](https://www.g2.com/survey_responses/grand-avenue-software-review-13171047) **["Easy-to-Follow Workflows and Straightforward eQMS Implementation"](https://www.g2.com/survey_responses/grand-avenue-software-review-13155767)** **Rating:** 5.0/5.0 stars _— Natasha O._ [Read full review](https://www.g2.com/survey_responses/grand-avenue-software-review-13155767) #### What Are G2 Users Discussing About Grand Avenue Software? - [What is Grand Avenue Software used for?](https://www.g2.com/discussions/what-is-grand-avenue-software-used-for) ### [Arena PLM & QMS](https://www.g2.com/products/arena-plm-qms/reviews) 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 and mitigate component issues throughout the product lifecycle, as well as 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 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:** 452 #### How Do G2 Users Rate Arena PLM & QMS? - **Has the product been a good partner in doing business?:** 8.9/10 (Category avg: 9.1/10) - **Design Controls:** 8.3/10 (Category avg: 8.5/10) - **Quality Processes:** 8.6/10 (Category avg: 9.0/10) - **Audit Management:** 8.3/10 (Category avg: 8.6/10) #### Who Is the Company Behind Arena PLM & QMS? - **Seller:** [PTC](https://www.g2.com/sellers/ptc) - **Company Website:** www.ptc.com - **Year Founded:** 1985 - **HQ Location:** Boston, Massachusetts - **Twitter:** @PTC 37,560 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=2562b24957155b8473247eb4a4b81fe707ca04fac9fc006da5825ec0a8c5e255&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F1935%2F&secure%5Burl_type%5D=linkedin_company_website) 8,145 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 **extremely easy to use** , with quick learning curves and responsive support. - Users value the **convenient document management** features of Arena PLM & QMS, enhancing organization and efficiency. - Users value the **secure document control** in Arena PLM & QMS that enhances team collaboration and compliance. - Users highlight the **intuitive interface** of Arena PLM & QMS, making it easy to navigate for everyone. - Users value the **responsive customer support** of Arena PLM & QMS, consistently receiving timely assistance with concerns. ##### Cons - Users feel frustrated by **feature limitations** , needing better ERP integration and enhancements for improved usability and tracking. - Users find Arena PLM & QMS lacking in **essential features** , such as multi-item search and improved template creation. - Users struggle with **ineffective search functionality** and difficulties in maintaining data consistency across the organization. - Users find the **inefficient searching** in Arena PLM & QMS frustrating, as it limits their ability to locate items easily. - Users find the **search functionality lacking** , struggling to locate multiple items or documents effectively within Arena PLM & QMS. #### What Are Recent G2 Reviews of Arena PLM & QMS? **["Arena PLM: A Scalable, Well-Organized Platform for Growing Teams"](https://www.g2.com/survey_responses/arena-plm-qms-review-13169022)** **Rating:** 4.0/5.0 stars _— Verified User in Electrical/Electronic Manufacturing_ [Read full review](https://www.g2.com/survey_responses/arena-plm-qms-review-13169022) **["Robust, Scalable Cloud PLM with Great Support and Onshape Integration"](https://www.g2.com/survey_responses/arena-plm-qms-review-13145402)** **Rating:** 5.0/5.0 stars _— Rob T._ [Read full review](https://www.g2.com/survey_responses/arena-plm-qms-review-13145402) #### What Are G2 Users Discussing About Arena PLM & QMS? - [What is Arena PLM & QMS used for?](https://www.g2.com/discussions/what-is-arena-plm-qms-used-for) - 1 comment - [What is the difference between ALM and PLM?](https://www.g2.com/discussions/what-is-the-difference-between-alm-and-plm) - 1 comment - [What is PLM in supply chain?](https://www.g2.com/discussions/what-is-plm-in-supply-chain) - 1 comment - [What does a PLM do?](https://www.g2.com/discussions/what-does-a-plm-do) - 2 comments - [How Much Does Arena PLM cost?](https://www.g2.com/discussions/how-much-does-arena-plm-cost) - 1 comment ### [QT9 QMS](https://www.g2.com/products/qt9-qms/reviews) 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:** 125 #### 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) - **Design Controls:** 8.2/10 (Category avg: 8.5/10) - **Quality Processes:** 9.3/10 (Category avg: 9.0/10) - **Audit Management:** 8.8/10 (Category avg: 8.6/10) #### Who Is the Company Behind QT9 QMS? - **Seller:** [QT9 Software](https://www.g2.com/sellers/qt9-software) - **Company Website:** qt9software.com - **Year Founded:** 2005 - **HQ Location:** Aurora, Illinois - **Twitter:** @Qt9Software 26 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=07270194debe81b701af8df72ac40cc5d4de72c71cff3959733b2cb77ab22b65&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fqt9-software%2F&secure%5Burl_type%5D=linkedin_company_website) 67 employees on LinkedIn® #### Who Uses This Product? - **Who Uses This:** Quality Manager, Quality Assurance Manager - **Top Industries:** Medical Devices, Manufacturing - **Company Size:** 54% Medium, 45% Small #### What Do G2 Reviewers Say About QT9 QMS? _AI-generated summary from verified user reviews_ ##### Pros - Users praise QT9 QMS for its **intuitive ease of use** , facilitating quick adoption and minimizing training needs. - Users commend the **responsive and knowledgeable customer support** of QT9 QMS, enhancing their overall experience with the platform. - Users value the **ease of setup and intuitive design** of QT9 QMS, facilitating swift implementation for MDSW launches. - Users value the **modular document control** in QT9 QMS, enhancing visibility, accountability, and compliance effortlessly. - Users value the **modular integration** of QT9 QMS, enhancing efficiency and supporting smoother quality management processes. ##### Cons - Users express frustration with **module setup issues** due to prerequisites that complicate implementation, especially for startups. - Users find the **complex setup** of QT9 QMS time-consuming and challenging, impacting initial usability. - Users note **feature limitations** in QT9 QMS, particularly in calibration options and record linking capabilities. - Users find the **learning difficulty** of QT9 QMS challenging due to its busy interface and prerequisite setups. - Users feel that QT9 QMS lacks **limited flexibility** , wishing for more customization options for their specific processes. #### What Are Recent G2 Reviews of QT9 QMS? **["QT9 QMS Makes Audits, CAPA, and Training Records Easy to Manage"](https://www.g2.com/survey_responses/qt9-qms-review-12667729)** **Rating:** 4.5/5.0 stars _— Stefanie C._ [Read full review](https://www.g2.com/survey_responses/qt9-qms-review-12667729) **["Excellent Training, Document Control, and CAPA Modules"](https://www.g2.com/survey_responses/qt9-qms-review-12955172)** **Rating:** 5.0/5.0 stars _— Renea K._ [Read full review](https://www.g2.com/survey_responses/qt9-qms-review-12955172) #### What Are G2 Users Discussing About QT9 QMS? - [What is QT9 QMS used for?](https://www.g2.com/discussions/what-is-qt9-qms-used-for) - 2 comments, 1 upvote ### [SimplerQMS](https://www.g2.com/products/simplerqms/reviews) SimplerQMS is an expert-driven electronic Quality Management System (eQMS) purpose-built for Life Science organizations. Our eQMS is designed by professionals with deep industry experience and supports compliance with FDA, ISO, and GxP requirements through automated, audit-ready quality processes. The platform centralizes and automates core quality workflows within a cloud-based, fully validated system. Customers benefit from reduced manual work, fewer errors, and consistently organized, inspection-ready records. Unlike generic QMS tools, SimplerQMS comes pre-configured for Life Science needs, with built-in templates, workflows, and controls aligned with FDA 21 CFR Part 11, 210/211, 820, EU Annex 11, ISO 13485:2016, and other applicable standards. Beyond software, customers gain a trusted partner backed by deep regulatory and quality expertise. This includes: • Audit-proven insights • Guidance from compliance specialists • Continuous system validation • Unlimited user training • 24/7 customer support • Smooth implementation and data migration • Dedicated Customer Success Experts With a mission to help Life Science companies manage quality and regulatory documentation efficiently, SimplerQMS supports organizations from early-stage growth to global scale to strengthen compliance, operational control, and quality culture. **Average Rating:** 4.9/5.0 **Total Reviews:** 13 #### How Do G2 Users Rate SimplerQMS? - **Has the product been a good partner in doing business?:** 9.6/10 (Category avg: 9.1/10) - **Design Controls:** 8.3/10 (Category avg: 8.5/10) - **Quality Processes:** 9.8/10 (Category avg: 9.0/10) - **Audit Management:** 8.7/10 (Category avg: 8.6/10) #### Who Is the Company Behind SimplerQMS? - **Seller:** [SimplerQMS](https://www.g2.com/sellers/simplerqms) - **Company Website:** www.simplerqms.com - **Year Founded:** 2017 - **HQ Location:** København, DK - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=9d988c0065043fde3fd4dedf0cc314ff3b7a35771d8941eddf91b47cd64bd084&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsimplerqms%2F&secure%5Burl_type%5D=linkedin_company_website) 80 employees on LinkedIn® #### Who Uses This Product? - **Top Industries:** Medical Devices - **Company Size:** 86% Small, 7% Medium #### What Do G2 Reviewers Say About SimplerQMS? _AI-generated summary from verified user reviews_ ##### Pros - Users commend the **excellent customer support** of SimplerQMS, highlighting responsiveness and helpfulness in addressing their needs. - Users value the **user-friendly interface** of SimplerQMS, which enhances efficiency in daily quality tasks. - Users love the **intuitive interface** of SimplerQMS, enhancing efficiency in daily quality management tasks. - Users appreciate the **straightforward implementation** of SimplerQMS, allowing for quick deployment and effective utilization in their processes. - Users commend SimplerQMS for its **effective document control** , enhancing compliance and streamlining document management processes. ##### Cons - Users find **feature limitations** in SimplerQMS, like one-way product-supplier relations and cumbersome document entries. - Users experience a **difficult installation** process that requires significant time and planning for effective setup. - Users find the **difficult usability** of SimplerQMS impacts their ability to efficiently access and utilize features. - Users find the **inefficient workflow** in SimplerQMS burdensome due to extra steps and non-intuitive terminology. - Users experience a **slight learning difficulty** initially, needing time to adapt to the system's features and workflows. #### What Are Recent G2 Reviews of SimplerQMS? **["Intuitive Interface and Outstanding Support Make SimplerQMS a Standout"](https://www.g2.com/survey_responses/simplerqms-review-12128025)** **Rating:** 5.0/5.0 stars _— Verified User in Medical Devices_ [Read full review](https://www.g2.com/survey_responses/simplerqms-review-12128025) **["Streamlined Compliance with Outstanding Training and Support"](https://www.g2.com/survey_responses/simplerqms-review-12402144)** **Rating:** 5.0/5.0 stars _— Cindi M._ [Read full review](https://www.g2.com/survey_responses/simplerqms-review-12402144) ### [Octave Reliance (ETQ Reliance)](https://www.g2.com/fr/products/octave-reliance-etq-reliance/reviews) Octave Reliance® (anciennement ETQ Reliance) est le principal fournisseur de logiciels de gestion de la qualité, de l'EHS et de la conformité, approuvé par les marques les plus fortes du monde. Plus de 600 clients à travers le monde, couvrant des industries telles que la fabrication, les dispositifs médicaux, l'électronique, l'industrie lourde, l'alimentation et les boissons, les produits pharmaceutiques et l'automobile, utilisent Reliance pour sécuriser des réputations de marque positives, permettre des niveaux plus élevés de fidélité des clients et améliorer la rentabilité. Octave Reliance offre des meilleures pratiques intégrées et une flexibilité puissante pour stimuler l'excellence commerciale grâce à la qualité. Reliance QMS fournit aux clients une suite de capacités fondamentales et un ensemble d'applications de base qui optimisent les programmes de gestion de la qualité : • Contrôle des documents • Gestion des changements • Gestion des audits • Action corrective (CAPA) • Insights Advanced Analytics • Gestion de la formation • Fournisseurs, matériaux et produits chimiques • Et plus encore Les clients de Reliance ont longtemps compté sur son portefeuille complet d'applications QMS intersectorielles pour faire progresser leurs programmes de qualité et atteindre des objectifs commerciaux critiques. Avec Reliance NXG, les clients peuvent désormais accélérer leur parcours qualité dans le monde résilient et adaptable de la gestion de la qualité et de la sécurité native du cloud, des analyses avancées, de l'accès omniprésent contrôlé et de la transformation numérique de l'entreprise. Reliance NXG permet aux clients de protéger efficacement l'avenir de leurs systèmes de gestion de la qualité et de fournir un puissant catalyseur à la transformation numérique dans leurs organisations. La fondation technologique de Reliance NXG repose sur quatre piliers de valeur : l'utilisabilité, la flexibilité, la visibilité et l'évolutivité, rendus possibles par des technologies avancées natives du cloud et une vision transformationnelle. • Utilisabilité : La nouvelle capacité de recherche de la solution permet aux utilisateurs de trouver rapidement n'importe quoi dans le système, avec une navigation améliorée pour rationaliser l'expérience utilisateur depuis n'importe quel appareil. • Flexibilité : De nouvelles fonctionnalités d'intégration, basées sur une architecture multi-locataire, permettent aux clients de briser les barrières qui limitent la collaboration et de suivre les changements dans leur entreprise. • Visibilité : Les efforts de transformation numérique pousseront les solutions QMS plus profondément dans la pile technologique d'entreprise d'une organisation. Alimentés par les analyses Insights, les flux de travail peuvent être configurés pour classer automatiquement les événements, améliorant la rapidité et la précision des décisions. Les utilisateurs ne reçoivent pas seulement de meilleures informations, mais aussi des conseils qui peuvent être utilisés pour rationaliser les enquêtes et les analyses des causes profondes. • Évolutivité : Le QMS natif du cloud permet des processus de qualité à l'échelle de l'entreprise, offrant un support pour n'importe quel nombre d'utilisateurs, n'importe quel volume de données et n'importe quelle configuration avec une architecture à haute disponibilité sans point de défaillance unique. Les clients des marchés réglementés peuvent tirer parti de la validation accélérée et de la vérification basée sur les risques dans Reliance pour réduire l'effort de test requis. Octave Reliance a été fondée à l'origine en 1992 sous le nom d'ETQ et a ses principaux bureaux situés aux États-Unis et en Europe. Pour en savoir plus sur Octave Reliance et ses diverses offres de produits, visitez https://www.octave.com/products/asset-performance-management/reliance. **Average Rating:** 4.3/5.0 **Total Reviews:** 606 #### How Do G2 Users Rate Octave Reliance (ETQ Reliance)? - **the product a-t-il été un bon partenaire commercial?:** 8.1/10 (Category avg: 9.1/10) - **Contrôles de conception:** 8.1/10 (Category avg: 8.5/10) - **Processus qualité:** 8.3/10 (Category avg: 9.0/10) - **Gestion de l’audit:** 7.9/10 (Category avg: 8.6/10) #### Who Is the Company Behind Octave Reliance (ETQ Reliance)? - **Vendeur:** [Octave](https://www.g2.com/fr/sellers/octave-9e5a428c-f303-4735-9417-dff1ef5736d4) - **Site Web de l'entreprise:** www.octave.com - **Emplacement du siège social:** Madison, US - **Page LinkedIn®:** [www.linkedin.com](https://www.g2.com/fr/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=430404c61b1403ac110b9bef1eccdb226c2d152f09d020a4c9da5926e5df6ee5&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Foctaveintelligence%2F&secure%5Burl_type%5D=linkedin_company_website) 3,001 employés sur LinkedIn® #### Who Uses This Product? - **Who Uses This:** Responsable Qualité, Ingénieur Qualité - **Top Industries:** Dispositifs médicaux, Pharmaceutique - **Company Size:** 50% Large, 42% Medium #### What Do G2 Reviewers Say About Octave Reliance (ETQ Reliance)? _AI-generated summary from verified user reviews_ ##### Pros - Les utilisateurs apprécient la **facilité d'utilisation** d'Octave Reliance, soulignant ses flux de travail simples et son administration pratique. - Les utilisateurs apprécient l' **interface conviviale et les fonctionnalités personnalisables** d'ETQ Reliance, améliorant la performance et l'interaction. - Les utilisateurs apprécient la **personnalisabilité** d'Octave Reliance, permettant des solutions sur mesure qui améliorent l'efficacité et la fonctionnalité organisationnelles. - Les utilisateurs apprécient les **options de personnalisation** d'Octave Reliance, améliorant l'utilisabilité et l'adaptant à leurs besoins spécifiques. - Les utilisateurs apprécient la **gestion documentaire conviviale** dans Octave Reliance, améliorant l'interaction et la performance à travers l'organisation. ##### Cons - Les utilisateurs trouvent que les **fonctionnalités manquantes** dans Octave Reliance entravent leur productivité et limitent considérablement la fonctionnalité. - Les utilisateurs soulignent les **limitations des fonctionnalités** dans ETQ Reliance, citant de mauvaises capacités mobiles et des options de personnalisation accablantes. - Les utilisateurs trouvent les **options de personnalisation limitées** frustrantes, entravant l'efficacité et compliquant le processus d'intégration. - Les utilisateurs expriment leur frustration face à **l'absence de fonctionnalités** dans Octave Reliance, en particulier en ce qui concerne les rapports et les capacités mobiles. - Les utilisateurs trouvent le **manque de convivialité** dans ETQ Reliance frustrant, surtout lors de l'intégration et de la personnalisation des flux de travail. #### What Are Recent G2 Reviews of Octave Reliance (ETQ Reliance)? **["Gestion de la qualité rationalisée sur une plateforme configurable"](https://www.g2.com/fr/survey_responses/octave-reliance-etq-reliance-review-13177775)** **Rating:** 4.0/5.0 stars _— Palkirat Kaur C._ [Read full review](https://www.g2.com/fr/survey_responses/octave-reliance-etq-reliance-review-13177775) **["Système parfait ETQ pour améliorer et promouvoir la qualité dans l'entreprise"](https://www.g2.com/fr/survey_responses/octave-reliance-etq-reliance-review-11059581)** **Rating:** 5.0/5.0 stars _— Madison S._ [Read full review](https://www.g2.com/fr/survey_responses/octave-reliance-etq-reliance-review-11059581) #### What Are G2 Users Discussing About Octave Reliance (ETQ Reliance)? - [What is ETQ Reliance QMS used for?](https://www.g2.com/fr/discussions/what-is-etq-reliance-qms-used-for) - [What is an electronic quality management system?](https://www.g2.com/fr/discussions/what-is-an-electronic-quality-management-system) - [Qu'est-ce que Qualio ?](https://www.g2.com/fr/discussions/etq-reliance-qms-what-is-qualio) - 2 comments - [Qu'est-ce que le logiciel EtQ ?](https://www.g2.com/fr/discussions/what-is-etq-software) - 1 comment - [What is EtQ reliance?](https://www.g2.com/fr/discussions/what-is-etq-reliance) ### [MasterControl Quality Management System](https://www.g2.com/fr/products/mastercontrol-quality-management-system/reviews) MasterControl Quality Excellence est le système de gestion de la qualité (QMS) numéro 1 dans les sciences de la vie. Construit sur une plateforme pilotée par l'IA, il permet aux entreprises des sciences de la vie de gérer de manière flexible les événements de qualité, de simplifier la gestion des documents et d'automatiser la gestion de la formation, le tout fonctionnant ensemble de manière transparente pour boucler la boucle sur la qualité. Principalement destiné aux professionnels de la qualité dans l'industrie des sciences de la vie, MasterControl Qx sert une gamme diversifiée d'organisations, allant des produits pharmaceutiques à la biotechnologie et aux dispositifs médicaux. Ces industries sont souvent confrontées à des exigences réglementaires strictes et à des processus d'assurance qualité complexes. MasterControl Qx offre une plateforme centralisée qui intègre diverses fonctions de gestion de la qualité, permettant aux utilisateurs de gérer les événements de qualité, la documentation, la formation et les audits de manière transparente. Cette intégration améliore non seulement l'efficacité opérationnelle, mais garantit également que les organisations restent conformes aux normes de l'industrie. L'une des caractéristiques remarquables de MasterControl Qx est ses capacités d'automatisation intelligente. En automatisant les tâches de gestion de la qualité de routine, les organisations peuvent réduire les erreurs manuelles et libérer un temps précieux pour que les professionnels de la qualité se concentrent sur des initiatives plus stratégiques. De plus, la plateforme fournit des informations robustes basées sur les données qui permettent aux utilisateurs de prendre des décisions éclairées basées sur des informations en temps réel. Cette approche axée sur les données améliore la capacité à identifier les tendances, à surveiller la conformité et à favoriser l'amélioration continue des processus de qualité. En outre, MasterControl Qx est conçu pour favoriser la collaboration entre les départements et les équipes. La nature connectée de la plateforme permet un partage facile des informations et de la documentation, garantissant que toutes les parties prenantes sont alignées et informées. Cet environnement collaboratif améliore non seulement la communication, mais soutient également une culture de la qualité dans toute l'organisation. En utilisant MasterControl Qx, les entreprises peuvent créer un système de gestion de la qualité plus agile et réactif qui s'adapte aux paysages réglementaires changeants et aux demandes du marché. Dans l'ensemble, MasterControl Quality Excellence (Qx) se distingue dans la catégorie des QMS en fournissant une solution holistique adaptée aux besoins spécifiques de l'industrie des sciences de la vie. Sa combinaison d'automatisation intelligente, d'informations robustes basées sur les données et de fonctionnalités collaboratives le positionne comme un outil précieux pour les organisations cherchant à maintenir des normes de qualité élevées tout en naviguant dans les complexités de la conformité réglementaire. **Average Rating:** 4.3/5.0 **Total Reviews:** 526 #### How Do G2 Users Rate MasterControl Quality Management System? - **the product a-t-il été un bon partenaire commercial?:** 8.8/10 (Category avg: 9.1/10) - **Contrôles de conception:** 7.1/10 (Category avg: 8.5/10) - **Processus qualité:** 8.0/10 (Category avg: 9.0/10) - **Gestion de l’audit:** 6.7/10 (Category avg: 8.6/10) #### Who Is the Company Behind MasterControl Quality Management System? - **Vendeur:** [MasterControl](https://www.g2.com/fr/sellers/mastercontrol) - **Site Web de l'entreprise:** www.mastercontrol.com - **Année de fondation:** 1993 - **Emplacement du siège social:** Salt Lake City, UT - **Twitter:** @MCMasterControl 6,258 abonnés Twitter - **Page LinkedIn®:** [www.linkedin.com](https://www.g2.com/fr/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=00588802c89147f00f07e6bed17054a50d4b885bbdcab7c82c6ef17d1397df09&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F23070%2F&secure%5Burl_type%5D=linkedin_company_website) 742 employés sur LinkedIn® #### Who Uses This Product? - **Who Uses This:** Spécialiste Assurance Qualité, Ingénieur Qualité - **Top Industries:** Pharmaceutique, Dispositifs médicaux - **Company Size:** 64% Medium, 25% Large #### What Do G2 Reviewers Say About MasterControl Quality Management System? _AI-generated summary from verified user reviews_ ##### Pros - Les utilisateurs apprécient la **facilité d'utilisation** de MasterControl, bénéficiant de son interface intuitive et de ses fonctionnalités personnalisables. - Les utilisateurs apprécient les fonctionnalités de **gestion centralisée des documents** de MasterControl, améliorant efficacement l'intégration et l'expérience utilisateur. - Les utilisateurs apprécient l' **intégration de formation conviviale** et le système centralisé pour gérer efficacement les événements de conformité et de qualité. - Les utilisateurs apprécient le **contrôle efficace des documents** dans MasterControl, appréciant l'accès facile aux documents et les mises à jour en temps opportun. - Les utilisateurs apprécient les **fonctionnalités personnalisables et conviviales** de MasterControl, facilitant des processus de gestion de la qualité efficaces. ##### Cons - Les utilisateurs trouvent **l'interface peu intuitive** , luttant avec des configurations complexes et une iconographie peu claire affectant l'expérience utilisateur. - Les utilisateurs rencontrent une **courbe d'apprentissage abrupte** avec MasterControl, en particulier lors de la configuration initiale et de la navigation entre les modules. - Les utilisateurs trouvent que la **difficulté d'utilisation** du système de MasterControl est un défi, en particulier pour la création de rapports et la configuration des flux de travail. - Les utilisateurs ont du mal avec l' **interface peu conviviale** de MasterControl, trouvant les fonctionnalités de navigation et de recherche lourdes et difficiles. - Les utilisateurs trouvent la **configuration complexe** difficile, nécessitant une formation approfondie pour utiliser efficacement les capacités de MasterControl. #### What Are Recent G2 Reviews of MasterControl Quality Management System? **["Parfait pour les entreprises des sciences de la vie !"](https://www.g2.com/fr/survey_responses/mastercontrol-quality-management-system-review-12477103)** **Rating:** 4.0/5.0 stars _— Sean M._ [Read full review](https://www.g2.com/fr/survey_responses/mastercontrol-quality-management-system-review-12477103) **["Gestion de documents pas seulement pour les sciences de la vie"](https://www.g2.com/fr/survey_responses/mastercontrol-quality-management-system-review-7875253)** **Rating:** 4.0/5.0 stars _— Travis B._ [Read full review](https://www.g2.com/fr/survey_responses/mastercontrol-quality-management-system-review-7875253) #### What Are G2 Users Discussing About MasterControl Quality Management System? - [À quoi sert le système de gestion de la qualité MasterControl ?](https://www.g2.com/fr/discussions/what-is-mastercontrol-quality-management-system-used-for) - 1 comment - [What is MasterControl Customer Complaints used for?](https://www.g2.com/fr/discussions/what-is-mastercontrol-customer-complaints-used-for) ### [sterloCare](https://www.g2.com/products/sterlo-sterlocare/reviews) sterloCare is a comprehensive healthcare digitization platform designed to enhance patient satisfaction and ensure compliance with regulatory standards such as NABH and JCI. Developed on a no-code platform, it enables hospitals to streamline operations across all departments, improving service quality and operational efficiency. The system seamlessly integrates with existing Hospital Information Systems (HIS) and offers flexible deployment options, including cloud and on-premise solutions. Accessible via desktops, tablets, and mobile devices, sterloCare provides real-time updates and supports role-based workflows with automated escalations to ensure timely task completion. Key Features and Functionality: - Service Request Management: Utilizes QR code-based triggers to efficiently manage service requests, track complaints, and gather patient feedback, facilitating prompt responses and improved patient care. - Digital Token System: Monitors outpatient journeys, reducing wait times and enhancing the overall patient experience. - Porter Management Software: Optimizes porter services, ensuring efficient patient transport within the hospital. - Automated Workflows and Escalations: Implements role-based workflows with built-in escalations, ensuring tasks are completed promptly and efficiently. - Real-Time Notifications: Delivers instant updates via mobile and email, keeping staff informed about task statuses and approvals. - Multilingual Support: Offers a user-friendly interface with support for multiple languages, catering to diverse regional needs. - Seamless Integration: Facilitates integration with existing HIS and other software systems, promoting efficient information flow and harmonious workflows. - Customizable Dashboards and Reports: Provides interactive dashboards and detailed reports, enabling data-driven decision-making and performance monitoring across departments. Primary Value and Solutions Provided: sterloCare addresses critical challenges in healthcare management by digitizing and automating various hospital processes. It enhances operational efficiency, reduces manual workloads, and ensures compliance with accreditation standards like NABH and JCI. By improving patient engagement through efficient service request handling and feedback mechanisms, sterloCare contributes to higher patient satisfaction. Its comprehensive reporting tools and real-time monitoring capabilities empower healthcare administrators to make informed decisions, ultimately leading to better patient outcomes and streamlined hospital operations. **Average Rating:** 4.7/5.0 **Total Reviews:** 21 #### How Do G2 Users Rate sterloCare? - **Design Controls:** 8.9/10 (Category avg: 8.5/10) - **Quality Processes:** 9.4/10 (Category avg: 9.0/10) - **Audit Management:** 9.6/10 (Category avg: 8.6/10) #### Who Is the Company Behind sterloCare? - **Seller:** [sterlo](https://www.g2.com/sellers/sterlo-a4c301d4-2da5-4501-aeb2-f54421a73486) - **Year Founded:** 2019 - **HQ Location:** Erode, IN - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=9901b7808ed4703e16335f857a87576d4be7fd42976f9764754f9631ee6ff621&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsterlocare&secure%5Burl_type%5D=linkedin_company_website) 16 employees on LinkedIn® #### Who Uses This Product? - **Top Industries:** Hospital & Health Care - **Company Size:** 86% Large, 14% Medium #### What Do G2 Reviewers Say About sterloCare? _AI-generated summary from verified user reviews_ ##### Pros - Users praise the **ease of use** of sterloCare, allowing seamless integration and quick adaptation for all staff. - Users appreciate the **improved patient care** offered by sterloCare, enhancing service and satisfaction through real-time feedback. - Users value the **excellent customer support** of sterloCare, enhancing smooth operations and quick issue resolution. - Users appreciate the **efficient communication** features of sterloCare, enhancing transparency and coordination within porter operations. - Users value the **efficiency** of sterloCare, facilitating seamless operations and enhancing patient satisfaction across the medical center. ##### Cons - Users report **notification issues** with delays and missed alerts, suggesting improvements for better communication flow. - Users report **excessive notifications** can be overwhelming, and delays occur during busy times affecting user experience. - Users experience **messaging issues** with delays in notifications and queue updates, affecting overall efficiency. - Users experience **notification problems** , including missed alerts and delays in low network coverage areas. - Users face **connectivity issues** in low network areas, leading to missed notifications and a need for offline functionality. #### What Are Recent G2 Reviews of sterloCare? **["A very effective porter management system that improved our hospital operations"](https://www.g2.com/survey_responses/sterlocare-review-11988847)** **Rating:** 5.0/5.0 stars _— Hari H._ [Read full review](https://www.g2.com/survey_responses/sterlocare-review-11988847) **["Simple and Seamless Housekeeping Workflow"](https://www.g2.com/survey_responses/sterlocare-review-12027480)** **Rating:** 4.5/5.0 stars _— Vera B._ [Read full review](https://www.g2.com/survey_responses/sterlocare-review-12027480) ### [1factory](https://www.g2.com/products/1factory/reviews) 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:** 20 #### How Do G2 Users Rate 1factory? - **Has the product been a good partner in doing business?:** 10.0/10 (Category avg: 9.1/10) - **Design Controls:** 1.7/10 (Category avg: 8.5/10) - **Quality Processes:** 10.0/10 (Category avg: 9.0/10) - **Audit Management:** 6.7/10 (Category avg: 8.6/10) #### Who Is the Company Behind 1factory? - **Seller:** [1factory](https://www.g2.com/sellers/1factory) - **Year Founded:** 2011 - **HQ Location:** Milpitas, CA - **Twitter:** @1FactoryInc 130 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=2686c6e2a4a1d1b88eaa516cdf944a05d52d21f8503923e5f29bebb091cfdebf&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F2287768%2F&secure%5Burl_type%5D=linkedin_company_website) 21 employees on LinkedIn® #### Who Uses This Product? - **Top Industries:** Machinery - **Company Size:** 65% Small, 30% Medium #### What Do G2 Reviewers Say About 1factory? _AI-generated summary from verified user reviews_ ##### Pros - Users find 1factory to be **easy to learn and navigate** , making quality control efficient and user-friendly. - Users appreciate the **efficiency and user-friendly features** of 1factory, enhancing quality control and inspection processes. - Users love the **intuitive UI** of 1factory, making implementation and navigation quick and easy. - Users commend the **top-notch customer support** of 1factory, ensuring quick assistance and seamless software usage. - Users appreciate the **easy learning curve** of 1factory, making it accessible and intuitive for everyone. ##### Cons - Users find the **confusing interface** of 1Factory challenging, especially when accessing advanced features and navigating menus. - Users find the **difficult usability** in deleting or modifying old prints cumbersome and inefficient in 1factory. - Users find that **modifying old prints** can be cumbersome, especially with attached inspection report histories. - Users find that **editing difficulties** arise when deleting or modifying old prints with inspection reports history. - Users find the **steep learning curve** of 1Factory challenging, especially for navigating advanced features and menus. #### What Are Recent G2 Reviews of 1factory? **["1Factory Streamlines Data Collection and Communication the setup and customer service were excellent"](https://www.g2.com/survey_responses/1factory-review-12756617)** **Rating:** 5.0/5.0 stars _— Connor M._ [Read full review](https://www.g2.com/survey_responses/1factory-review-12756617) **["1Factory is 1Fantastic!! - Easy to Implement, Fast-Responding UI with Outstanding Visuals"](https://www.g2.com/survey_responses/1factory-review-12846846)** **Rating:** 5.0/5.0 stars _— John M._ [Read full review](https://www.g2.com/survey_responses/1factory-review-12846846) #### What Are G2 Users Discussing About 1factory? - [What is 1factory used for?](https://www.g2.com/discussions/what-is-1factory-used-for) - 1 comment ### [Greenlight Guru Quality Management System](https://www.g2.com/fr/products/greenlight-guru-quality-management-system/reviews) Greenlight Guru est le système de gestion de la qualité numéro 1 conçu exclusivement pour les entreprises de dispositifs médicaux. Pas pour les sciences de la vie. Pas pour la pharma avec une couche de configuration medtech. Parce que nous avons conçu exclusivement pour les dispositifs médicaux, ISO 13485, ISO 14971, et FDA QMSR ne sont pas des cadres que vous configurez après coup. Ils sont la fondation. La plupart des équipes qualité gèrent la conformité à travers des systèmes qui n'ont jamais été conçus pour communiquer entre eux. Un outil de contrôle des documents ici, un tableur pour les CAPA là, un processus séparé pour le contrôle des changements. Dans un environnement réglementé, cet écart ne reste pas invisible, il apparaît lors des audits. Greenlight Guru offre aux équipes Qualité et Produit un système unique et connecté où le contrôle des documents, la formation, les CAPA, la non-conformité, le contrôle des changements, la gestion des fournisseurs, la gestion des risques et les contrôles de conception fonctionnent ensemble. Lorsqu'un changement se produit, il circule à travers le flux de travail. Cela signifie des transferts manuels limités, et rien ne passe entre les mailles du filet entre les équipes. Pour les professionnels de la Qualité et des Affaires Réglementaires, cela signifie des flux de travail prêts pour l'audit avec routage automatisé, signatures électroniques et pistes d'audit complètes intégrées, y compris la traçabilité de bout en bout à travers les contrôles de conception. Plus besoin de courir après les approbations ou de suivre manuellement le statut de conformité. Les équipes qui fonctionnent sur Greenlight Guru ont 3,5 fois moins de chances de recevoir une constatation d'audit majeure. Pour les équipes R&D et produit, cela signifie rester dans les outils qu'elles utilisent déjà, avec des changements se synchronisant automatiquement aux contrôles de conception afin que la documentation se construise d'elle-même au fur et à mesure que vous travaillez, et non après coup comme un projet séparé. Greenlight Guru AI gère le travail répétitif qui ralentit les équipes, et il a été construit avec 15 ans de contexte medtech derrière lui, pas ajouté à partir d'un modèle à usage général. La recherche alimentée par l'IA trouve des réponses à travers votre QMS instantanément. Le chat analyse les données du système pour faire émerger des insights. Les résumés générés automatiquement donnent un contexte immédiat sur les documents, les fournisseurs et les événements de qualité. Pour les équipes produit, les vérifications de vérifiabilité attrapent les exigences vagues avant qu'elles ne deviennent des constatations d'audit, les liens suggérés comblent automatiquement les lacunes de traçabilité, et le brainstorming IA permet aux ingénieurs d'avancer plus rapidement. Pour les équipes qualité, l'IA génère des quiz de formation et rédige des résumés de commandes de changement, de sorte que votre équipe passe moins de temps à écrire et plus de temps sur le travail qui nécessite réellement leur expertise. La plateforme est validée dès la sortie de la boîte et alignée sur FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, EU MDR, et FDA 21 CFR Part 11. La mise en œuvre se mesure en semaines, pas en projets de plusieurs trimestres qui accompagnent les plateformes d'entreprise héritées. Soutenu par plus de 80 modèles personnalisables testés par audit et une équipe d'experts qui connaissent le medtech de fond en comble. Vous ne gérez pas un projet de validation séparé avant de pouvoir être opérationnel. Depuis 15 ans et à travers plus de 1 000 entreprises de dispositifs dans le monde entier, Greenlight Guru est le QMS auquel les équipes de dispositifs médicaux font confiance pour réussir les audits, mettre des produits sur le marché et y rester plus longtemps. **Average Rating:** 4.5/5.0 **Total Reviews:** 401 #### How Do G2 Users Rate Greenlight Guru Quality Management System? - **the product a-t-il été un bon partenaire commercial?:** 9.3/10 (Category avg: 9.1/10) - **Contrôles de conception:** 8.4/10 (Category avg: 8.5/10) - **Processus qualité:** 8.9/10 (Category avg: 9.0/10) - **Gestion de l’audit:** 8.3/10 (Category avg: 8.6/10) #### Who Is the Company Behind Greenlight Guru Quality Management System? - **Vendeur:** [Greenlight Guru](https://www.g2.com/fr/sellers/greenlight-guru) - **Site Web de l'entreprise:** www.greenlight.guru - **Année de fondation:** 2013 - **Emplacement du siège social:** Indianapolis, IN - **Twitter:** @greenlightguru 10,590 abonnés Twitter - **Page LinkedIn®:** [www.linkedin.com](https://www.g2.com/fr/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=7df50f335a6d5a650bbc46a24d2ab5da06b02fc852b348529906f73428faacd5&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F3837459%2F&secure%5Burl_type%5D=linkedin_company_website) 138 employés sur LinkedIn® #### Who Uses This Product? - **Who Uses This:** Responsable Qualité, Ingénieur Qualité - **Top Industries:** Dispositifs médicaux, Biotechnologie - **Company Size:** 79% Small, 20% Medium #### What Do G2 Reviewers Say About Greenlight Guru Quality Management System? _AI-generated summary from verified user reviews_ ##### Pros - Les utilisateurs trouvent que l'eQMS de Greenlight Guru est **intuitif et facile à utiliser** , améliorant la conformité et rationalisant les processus. - Les utilisateurs apprécient la **conception conviviale et les fonctionnalités de conformité robustes** de Greenlight Guru, améliorant leurs processus de gestion de la qualité. - Les utilisateurs louent les **outils de formation efficaces** de Greenlight Guru, facilitant une intégration rapide et la conformité aux normes de l'industrie. - Les utilisateurs apprécient les fonctionnalités de **gestion d'audit rationalisée** de Greenlight Guru, améliorant efficacement la conformité et l'organisation. - Les utilisateurs apprécient la **configurabilité** de Greenlight Guru, facilitant une organisation facile et une gestion efficace des processus de qualité. ##### Cons - Les utilisateurs trouvent que **les prix sont chers** , ce qui peut ne pas être compétitif pour de nombreuses équipes et ajoute de la frustration. - Les utilisateurs notent les **limitations des fonctionnalités** de Greenlight Guru, notamment en ce qui concerne la flexibilité et les projets supplémentaires coûteux. - Les utilisateurs trouvent que la **fonction de recherche actuelle est inefficace** , suggérant des améliorations comme l'IA pour une meilleure récupération d'informations. - Les utilisateurs trouvent que **l'inflexibilité des événements de qualité** dans Greenlight Guru perturbe leur flux de travail malgré son respect des exigences CAPA. - Les utilisateurs trouvent les **analyses limitées** , manquant de profondeur malgré l'offre de quelques aperçus de données utiles dans Greenlight Guru. #### What Are Recent G2 Reviews of Greenlight Guru Quality Management System? **["Greenlight Guru eQMS - année 5"](https://www.g2.com/fr/survey_responses/greenlight-guru-quality-management-system-review-7404775)** **Rating:** 5.0/5.0 stars _— Utilisateur vérifié à Dispositifs médicaux_ [Read full review](https://www.g2.com/fr/survey_responses/greenlight-guru-quality-management-system-review-7404775) **["Système de gestion de la qualité électronique simple, propre et efficace pour la conformité ISO 13485"](https://www.g2.com/fr/survey_responses/greenlight-guru-quality-management-system-review-12670075)** **Rating:** 4.0/5.0 stars _— Holly Lawrence O._ [Read full review](https://www.g2.com/fr/survey_responses/greenlight-guru-quality-management-system-review-12670075) #### What Are G2 Users Discussing About Greenlight Guru Quality Management System? - [Quel est le meilleur système de gestion de la qualité ?](https://www.g2.com/fr/discussions/what-is-the-best-quality-management-system) - 1 comment - [Qu'est-ce qu'un logiciel de système de gestion de la qualité ?](https://www.g2.com/fr/discussions/what-is-quality-management-system-software) - 1 comment - [How much does greenlight guru cost?](https://www.g2.com/fr/discussions/how-much-does-greenlight-guru-cost) - [Qu'est-ce que Greenlight Guru ?](https://www.g2.com/fr/discussions/what-is-greenlight-guru) - 2 comments ### [Orcanos](https://www.g2.com/products/orcanos/reviews) Orcanos is a modern MedTech eQMS platform designed to help regulated teams accelerate compliance, stay audit-ready, and streamline quality processes — from design to post-market. Unlike traditional QMS solutions, Orcanos also includes integrated development lifecycle tools (ALM), enabling full traceability across requirements, risks, testing, and quality in one system — without coding. Key Capabilities Document Control & Training CAPA, NCR, Complaints & Audits Risk Management (ISO 14971) Design Control / DHF / DMR Requirements & Test Management End-to-End Traceability Electronic Signatures & Validation Support (FDA, ISO, EU MDR) Why Orcanos Built for regulated hardware, MedTech & pharma Codeless workflows & fast implementation Unified quality + product development data **Average Rating:** 4.3/5.0 **Total Reviews:** 124 #### How Do G2 Users Rate Orcanos? - **Has the product been a good partner in doing business?:** 9.1/10 (Category avg: 9.1/10) - **Design Controls:** 8.4/10 (Category avg: 8.5/10) - **Quality Processes:** 8.6/10 (Category avg: 9.0/10) - **Audit Management:** 8.0/10 (Category avg: 8.6/10) #### Who Is the Company Behind Orcanos? - **Seller:** [Orcanos](https://www.g2.com/sellers/orcanos) - **Year Founded:** 2015 - **HQ Location:** Givatyim - **Twitter:** @orcanos 63 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=5f14d7c380d2bb8ec8c4a892b335a50b3c5fe8cfda125060970ec849404c2468&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Forcanos%2F&secure%5Burl_type%5D=linkedin_company_website) 38 employees on LinkedIn® #### Who Uses This Product? - **Top Industries:** Medical Devices, Hospital & Health Care - **Company Size:** 58% Small, 40% Medium #### What Do G2 Reviewers Say About Orcanos? _AI-generated summary from verified user reviews_ ##### Pros - Users commend Orcanos for their **exceptional customer support** , showcasing readiness to assist and resolve issues effectively. - Users commend the **ease of use** of Orcanos, highlighting its intuitive interface and excellent support for all skill levels. - Users value Orcanos for its **comprehensive tools** that enhance traceability and streamline product development processes effectively. - Users value the **high customization** options of Orcanos, allowing seamless adaptation to their unique processes and needs. - Users appreciate the **user-friendly document management** of Orcanos, benefiting from its intuitive and flexible interface. ##### Cons - Users find **feature limitations** in Orcanos, noting gaps in integrations, slow performance, and a lackluster export process. - Users note that **slow performance** with loading times and server responses hampers their overall Orcanos experience. - Users find the **learning curve steep** , complicating the use of Orcanos, especially during implementation and revision management. - Users find the **difficult usability** of Orcanos challenging, particularly with complex administration and limited user support. - Users find Orcanos to be **not intuitive** , struggling with its complex UI that obscures essential content and files. #### What Are Recent G2 Reviews of Orcanos? **["Highly Customizable Solution That Adapts to Your Workflow"](https://www.g2.com/survey_responses/orcanos-review-11906568)** **Rating:** 4.0/5.0 stars _— Verified User in Medical Devices_ [Read full review](https://www.g2.com/survey_responses/orcanos-review-11906568) **["Highly Adjustable and User-Friendly Platform"](https://www.g2.com/survey_responses/orcanos-review-7052884)** **Rating:** 5.0/5.0 stars _— Shay N._ [Read full review](https://www.g2.com/survey_responses/orcanos-review-7052884) #### What Are G2 Users Discussing About Orcanos? - [How has Orcanos supported your quality management and compliance needs, and what features do you rely on?](https://www.g2.com/discussions/how-has-orcanos-supported-your-quality-management-and-compliance-needs-and-what-features-do-you-rely-on) - [What is Orcanos used for?](https://www.g2.com/discussions/what-is-orcanos-used-for) ### [AmpleLogic Electronic Quality Management System (eQMS)](https://www.g2.com/products/amplelogic-electronic-quality-management-system-eqms/reviews) AmpleLogic’s eQMS software is specially crafted for highly regulated sectors such as Lifesciences, Medical Devices, Food & Beverages, Beauty and Cosmetics, Gene Therapy and so on. AL’s eQMS software renders 11 specific modules: CAPA, Change Control, Market Complaints, Deviations, Audits, Vendor Qualification, Out of Specification, Out of Trend, Lab Incident Reporting. All these modules are seamlessly integrated with one another. AmpleLogic also has other COTS products like Data Management System (DMS), Learning Management System (LMS), Regulatory Information Management System (RIMS), Electronic Batch Management System (eBMR), Environmental Monitoring Software (EMS), etc that are integrated with eQMS to offer best quality management! Benefits:  Perks of a Low-Code-No-Code QMS  Customized to your needs  Manual work reduced  Keeps track of quality concerns across departments  Centralized repository for quality records  Be assessment ready  Provides Quality Metric Analysis guided by KPIs  Pending Task Feature at each level  Customized dashboards  Realtime Insights  History report  483 issue compliance (USFD)  Alcoa+ Principles compliance  Cost Effective modifications and approvals **Average Rating:** 4.9/5.0 **Total Reviews:** 85 #### How Do G2 Users Rate AmpleLogic Electronic Quality Management System (eQMS)? - **Has the product been a good partner in doing business?:** 9.8/10 (Category avg: 9.1/10) - **Design Controls:** 9.4/10 (Category avg: 8.5/10) - **Quality Processes:** 9.6/10 (Category avg: 9.0/10) - **Audit Management:** 9.5/10 (Category avg: 8.6/10) #### Who Is the Company Behind AmpleLogic Electronic Quality Management System (eQMS)? - **Seller:** [AmpleLogic](https://www.g2.com/sellers/amplelogic) - **Year Founded:** 2010 - **HQ Location:** Hyderabad, Telangana - **Twitter:** @Ample\_Logic 636 Twitter followers - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=3246b9b1f3c515fa97614cffcb695872158b221aee65a7dac379dd9bd4e2b4be&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fample-logic%2F&secure%5Burl_type%5D=linkedin_company_website) 322 employees on LinkedIn® #### Who Uses This Product? - **Top Industries:** Pharmaceuticals, Manufacturing - **Company Size:** 92% Medium, 4% Large #### What Do G2 Reviewers Say About AmpleLogic Electronic Quality Management System (eQMS)? _AI-generated summary from verified user reviews_ ##### Pros - Users appreciate the **excellent customer support** from AmpleLogic eQMS, making setup and usage seamless and efficient. - Users value the **ease of use** of AmpleLogic eQMS, appreciating its user-friendly interface and efficient functionalities. - Users appreciate the **intuitive design and effective dashboards** of AmpleLogic eQMS, enhancing usability and efficiency. - Users appreciate the **implementation ease** of AmpleLogic eQMS, highlighting its user-friendly interface and helpful technical support. - Users commend the **efficient search functionality** of AmpleLogic eQMS, making access to records quick and effective. #### What Are Recent G2 Reviews of AmpleLogic Electronic Quality Management System (eQMS)? **["Highly Configurable eQMS That Aligns Perfectly With Our Quality Processes"](https://www.g2.com/survey_responses/amplelogic-electronic-quality-management-system-eqms-review-13028164)** **Rating:** 4.5/5.0 stars _— Lalit N._ [Read full review](https://www.g2.com/survey_responses/amplelogic-electronic-quality-management-system-eqms-review-13028164) **["QMS SYSTEM"](https://www.g2.com/survey_responses/amplelogic-electronic-quality-management-system-eqms-review-8994271)** **Rating:** 5.0/5.0 stars _— Avinash M._ [Read full review](https://www.g2.com/survey_responses/amplelogic-electronic-quality-management-system-eqms-review-8994271) ### [Kivo](https://www.g2.com/products/kivo/reviews) Kivo is building the infrastructure for GxP compliance in the era of AI-powered drug development. Its unified cloud platform supports Regulatory, Clinical, and Quality operations — including RIM, eTMF, QMS, controlled document management, submission assembly, eCTD lifecycle management, inspection readiness, SOP management, and training management — within a single, audit-ready environment. With Part 11-compliant e-signatures, role-based permissions, continuous validation assurance, and a lossless data model that preserves context from legacy systems, Kivo gives life sciences teams the compliant foundation to reduce operational friction and accelerate time to market. ▶ For Regulatory • Customizable, automatic authoring, review, QC, and approval workflows • Real-time collaboration online or locally in Office 365 • Smart document placeholders, with pre-formatted ICH templates available • Assemble submissions from pre-built submission structures aligned to country guidelines • Create automated tracking spreadsheets for external publishing groups ▶ For Quality • Controlled document and SOP management that meets GxP standards • Training management linked directly to documents in the DMS • Build curricula for teams or individual users with documents, videos, and quizzes • Auto-fill quality forms with metadata • Manage change controls, CAPAs, Deviations, Audits, and Vendors ▶ For Clinical • Workflows mapped to the TMF reference model • Accelerate active trial management, from study start up and beyond • Migrate TMFs into the system in weeks, including recompiled audit trails • Real-time reporting into TMF completeness • Long-term TMF storage at a fraction of the typical cost, with automatic checksums to ensure data integrity • Separate inspector access to help streamline your trial narrative **Average Rating:** 4.9/5.0 **Total Reviews:** 20 #### How Do G2 Users Rate Kivo? - **Has the product been a good partner in doing business?:** 10.0/10 (Category avg: 9.1/10) - **Quality Processes:** 10.0/10 (Category avg: 9.0/10) - **Audit Management:** 10.0/10 (Category avg: 8.6/10) #### Who Is the Company Behind Kivo? - **Seller:** [Kivo](https://www.g2.com/sellers/kivo) - **Company Website:** kivo.io - **Year Founded:** 2021 - **HQ Location:** Portland, US - **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=77800174ab31242ee73d16023e24a33fc267a57870a2980ed57490a50393d799&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fkivoio&secure%5Burl_type%5D=linkedin_company_website) 43 employees on LinkedIn® #### Who Uses This Product? - **Top Industries:** Biotechnology, Pharmaceuticals - **Company Size:** 65% Small, 35% Medium #### What Do G2 Reviewers Say About Kivo? _AI-generated summary from verified user reviews_ ##### Pros - Users value the **ease of use** of Kivo, appreciating its intuitive design and minimal learning curve. - Users value the **implementation ease** of Kivo, appreciating fast setup and excellent customer support throughout the process. - Users praise Kivo's **intuitive interface and organization** , making navigation effortless even for first-time users. - Users commend Kivo for its **excellent customer support** , enhancing the overall experience and ensuring smooth implementation. - Users value the **customization options** in Kivo, enabling tailored functionality that meets diverse organizational needs effectively. ##### Cons - Users find the **feature limitations** of Kivo frustrating, needing workarounds for incomplete functionalities like electronic signatures. - Users find the **missing features** in Kivo frustrating, needing workarounds for tasks like electronic signatures. - Users find the **left-side navigation confusing** , which hinders their overall experience with Kivo. #### What Are Recent G2 Reviews of Kivo? **["Intuitive, Fast, and Highly Customizable DMS with Exceptional Support"](https://www.g2.com/survey_responses/kivo-review-12757149)** **Rating:** 4.5/5.0 stars _— Mike M._ [Read full review](https://www.g2.com/survey_responses/kivo-review-12757149) **["Intuitive Interface That Saves Time, Money, and Effort"](https://www.g2.com/survey_responses/kivo-review-12756771)** **Rating:** 4.5/5.0 stars _— Andy W._ [Read full review](https://www.g2.com/survey_responses/kivo-review-12756771) - ‹ Prev‹ Prev - 1 - [2](/categories/medical-qms?open_modal_url=%2Fproducts%2Falmond%2Fwishlists%3Fhost_path%3D%252Fcategories%252Fmedical-qms%26source%3Dcategory&order=g2_score&page=2#product-list) - [3](/categories/medical-qms?open_modal_url=%2Fproducts%2Falmond%2Fwishlists%3Fhost_path%3D%252Fcategories%252Fmedical-qms%26source%3Dcategory&order=g2_score&page=3#product-list) - [4](/categories/medical-qms?open_modal_url=%2Fproducts%2Falmond%2Fwishlists%3Fhost_path%3D%252Fcategories%252Fmedical-qms%26source%3Dcategory&order=g2_score&page=4#product-list) - [5](/categories/medical-qms?open_modal_url=%2Fproducts%2Falmond%2Fwishlists%3Fhost_path%3D%252Fcategories%252Fmedical-qms%26source%3Dcategory&order=g2_score&page=5#product-list) - … - [8](/categories/medical-qms?open_modal_url=%2Fproducts%2Falmond%2Fwishlists%3Fhost_path%3D%252Fcategories%252Fmedical-qms%26source%3Dcategory&order=g2_score&page=8#product-list) - [9](/categories/medical-qms?open_modal_url=%2Fproducts%2Falmond%2Fwishlists%3Fhost_path%3D%252Fcategories%252Fmedical-qms%26source%3Dcategory&order=g2_score&page=9#product-list) - [Next ›Next ›](/categories/medical-qms?open_modal_url=%2Fproducts%2Falmond%2Fwishlists%3Fhost_path%3D%252Fcategories%252Fmedical-qms%26source%3Dcategory&order=g2_score&page=2#product-list) Spotlight Categories [Social Media Management Tools](https://www.g2.com/categories/social-media-mgmt) [Robotic Process Automation (RPA) Software](https://www.g2.com/categories/robotic-process-automation-rpa) [Sales Tax and VAT Compliance Software](https://www.g2.com/categories/sales-tax-and-vat-compliance) [Identity and Access Management (IAM) Software](https://www.g2.com/categories/identity-and-access-management-iam) [HCM Software](https://www.g2.com/categories/hcm-software) Similar Categories - [Clinical Research](/categories/clinical-research) - [Drug Discovery](/categories/drug-discovery) - [Other Life Sciences](/categories/other-life-sciences) - [Pharma and Biotech](/categories/pharma-and-biotech) - [Regulatory Information Management (RIM) Systems](/categories/regulatory-information-management-rim-systems) [Browse Medical QMS Themes](/categories/medical-qms/themes) ![Emma Stein](/assets/transparent-ad5be28fbcd25b7b08d2cebe1d957125437fb5407d75ee717965ad22c8808791.gif "Emma Stein") ES Researched and written by [Emma Stein](https://research.g2.com/insights/author/emma-stein) Updated October 3, 2024 For highly regulated industries like life sciences and pharma, industry-specific quality management systems (QMS) address the complex product development lifecycle of pharmaceutical, biotech, and medical devices products. Medical Quality Management Systems (QMS) are designed to facilitate compliance with regulations enacted by the FDA and standards like ISO 13485 (the International Organization for Standardization specific to medical devices). Additionally, with a medical QMS, life science businesses can eliminate paper-based quality processes, improve product quality and safety, reduce overall costs, increase operational efficiency, and unify and standardize processes, documentation, and communication. If you are looking for a quality system that facilitates the standardization and maintenance of standard operating procedures (SOP) or internal business processes, take a look at the [healthcare compliance software](https://www.g2.com/categories/healthcare-compliance). Additionally, some horizontal [quality management software](https://www.g2.com/categories/quality-management-qms) solutions can be, and are, used for less complicated quality processes for pharmaceutical, biotech, and medical device products. To qualify for inclusion in the Medical Quality Management Systems (QMS) category, a product must: - Provide product traceability functionality - Track and document every event and process that occurs during the product lifecycle - Monitor industry regulation and set up reminders or triggers for potential violations - Capture customer complains to assess and manage risk - Facilitate product testing and inspections - Provide support and workflows for corrective actions to tested products Top Tools at a Glance | Product | Best for | User Review | | --- | --- | --- | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_239fdb020d69919db5553a9bf0b0e605/qualio.jpg "Product Avatar Image")](https://www.g2.com/products/qualio/reviews)[Qualio](https://www.g2.com/products/qualio/reviews)[4.4/5(781)](https://www.g2.com/products/qualio/reviews) | Regulated QMS document control with audit-ready traceability | "It makes my onboarding life easier" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_9aa08b07a3f9ed6c6c419b969f9eb9f1/kneat-gx.jpg "Product Avatar Image")](https://www.g2.com/products/kneat-gx/reviews)[Kneat Gx](https://www.g2.com/products/kneat-gx/reviews)[4.5/5(98)](https://www.g2.com/products/kneat-gx/reviews) | Paperless CQV execution with end-to-end traceability | "Will transform your traditional validation program and processes" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_60c9e8bac3ab1b560dc50c861471b629/honeywell-trackwise.png "Product Avatar Image")](https://www.g2.com/products/honeywell-trackwise/reviews)[TrackWise Enterprise Quality Management Software](https://www.g2.com/products/honeywell-trackwise/reviews)[4.3/5(48)](https://www.g2.com/products/honeywell-trackwise/reviews) | GxP deviation, CAPA, and change-control tracking | "Trackwise good for tracking all QMS record and user friendly.All QMS records available in excelsheet" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_62ce07a97b655c6f93cfa06af1edb429/arena-plm-qms.png "Product Avatar Image")](https://www.g2.com/products/arena-plm-qms/reviews)[Arena PLM & QMS](https://www.g2.com/products/arena-plm-qms/reviews)[4.2/5(463)](https://www.g2.com/products/arena-plm-qms/reviews) | Regulated device change control with BOM traceability | "Arena PLM: A Scalable, Well-Organized Platform for Growing Teams" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_1441f4aff10b95e35af0b8e20d46fe40/qt9-qms.png "Product Avatar Image")](https://www.g2.com/products/qt9-qms/reviews)[QT9 QMS](https://www.g2.com/products/qt9-qms/reviews)[4.8/5(125)](https://www.g2.com/products/qt9-qms/reviews) | ISO 13485 compliance with concurrent-user licensing | "Excellent Training, Document Control, and CAPA Modules" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_fd30c704eb9c2cd7680e5f2a9ddbcc05/simplerqms.png "Product Avatar Image")](https://www.g2.com/products/simplerqms/reviews)[SimplerQMS](https://www.g2.com/products/simplerqms/reviews)[4.9/5(14)](https://www.g2.com/products/simplerqms/reviews) | Pre-validated eQMS for life sciences compliance | "Intuitive Interface and Outstanding Support Make SimplerQMS a Standout" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_a513aeb0071452bcac141bfc8cae8b39/octave-reliance-etq-reliance.png "Product Avatar Image")](https://www.g2.com/products/octave-reliance-etq-reliance/reviews)[Octave Reliance (ETQ Reliance)](https://www.g2.com/products/octave-reliance-etq-reliance/reviews)[4.3/5(624)](https://www.g2.com/products/octave-reliance-etq-reliance/reviews) | Configurable eQMS with cross-module CAPA traceability | "Streamlined Quality Management in One Configurable Platform" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_952e9aa4df0af1b0706297e2afcb725f/mastercontrol-quality-management-system.png "Product Avatar Image")](https://www.g2.com/products/mastercontrol-quality-management-system/reviews)[MasterControl](https://www.g2.com/products/mastercontrol-quality-management-system/reviews)[4.3/5(528)](https://www.g2.com/products/mastercontrol-quality-management-system/reviews) | Regulated QMS document control and CAPA traceability | "Perfect for life sciences companies!" | | [![Product Avatar Image](https://images.g2crowd.com/uploads/product/image/large_detail/large_detail_16b6a6adc260c93446e6d331cf3d7a9a/sterlo-sterlocare.jpg "Product Avatar Image")](https://www.g2.com/products/sterlo-sterlocare/reviews)[sterloCare](https://www.g2.com/products/sterlo-sterlocare/reviews)[4.7/5(21)](https://www.g2.com/products/sterlo-sterlocare/reviews) | QR-based hospital complaint and CAPA workflows | "A very effective porter management system that improved our hospital operations" | * * * Show More