# Best Medical Quality Management Systems (QMS) - Page 4

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

**Total Products under this Category:** 121

### Category Stats (Jul 2026)

- **Average Rating:** 4.39/5 (↑0.01 vs Jun 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: July 31, 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=1470&focus%5B%5D=1255729&focus%5B%5D=50982&focus%5B%5D=39899&focus%5B%5D=1500618)

Highlighted products: Qualio, Kneat Gx, TrackWise, Arena PLM & QMS, SimplerQMS, QT9 QMS, Octave Reliance (ETQ Reliance), and sterloCare.

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=arena-plm-qms&focus%5B%5D=simplerqms&focus%5B%5D=qt9-qms&focus%5B%5D=octave-reliance-etq-reliance&focus%5B%5D=sterlo-sterlocare)

**Sponsored**

### Greenlight Guru Quality Management System

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

[Visit website](https://www.g2.com/external_clickthroughs/record?secure%5Bad_program%5D=paid_promo&secure%5Bad_slot%5D=category_product_list_llm&secure%5Bcategory_id%5D=1884&secure%5Bchosen_at%5D=2026-08-01T02%3A15%3A30Z&secure%5Bmedium%5D=sponsored&secure%5Bprioritized%5D=false&secure%5Bproduct_id%5D=15578&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%3Fpage%3D4&secure%5Btoken%5D=976b2a78f035aa0b429263813598440234d3ed9a1679f1b085bf39d28ce8f514&secure%5Burl%5D=https%3A%2F%2Fwww.greenlight.guru%2Fquality-management-software&secure%5Burl_type%5D=paid_promos)

### [FFReporting Pharmaceuticals](https://www.g2.com/products/ffreporting-pharmaceuticals/reviews)

FFReporting Sales Force Automation (SFA) provides various features which also helps to propel your business.

**Average Rating:** 5.0/5.0

**Total Reviews:** 1

#### How Do G2 Users Rate FFReporting Pharmaceuticals?

- **Has the product been a good partner in doing business?:** 10.0/10 (Category avg: 9.1/10)
- **Design Controls:** 8.3/10 (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 FFReporting Pharmaceuticals?

- **Seller:** [Sarjen System](https://www.g2.com/sellers/sarjen-system)
- **Year Founded:** 1998
- **HQ Location:** N/A
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=ceab8a44a8b52be607ebfe47559a8dd9198210eba11c1b1093dafe117a5aa0b6&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2F1007381&secure%5Burl_type%5D=linkedin_company_website)  
369 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Medium

#### What Are Recent G2 Reviews of FFReporting Pharmaceuticals?

**["Patient life"](https://www.g2.com/survey_responses/ffreporting-pharmaceuticals-review-2602044)**

**Rating:** 5.0/5.0 stars

_— Shadrack M._

[Read full review](https://www.g2.com/survey_responses/ffreporting-pharmaceuticals-review-2602044)

#### What Are G2 Users Discussing About FFReporting Pharmaceuticals?

- [What is FFReporting Pharmaceuticals used for?](https://www.g2.com/discussions/what-is-ffreporting-pharmaceuticals-used-for)

### [LabWay-LIMS](https://www.g2.com/products/labway-lims/reviews)

LabWay-LIMS is an full integrated solution for analysis laboratory management solution.

**Average Rating:** 3.5/5.0

**Total Reviews:** 1

#### How Do G2 Users Rate LabWay-LIMS?

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

#### Who Is the Company Behind LabWay-LIMS?

- **Seller:** [Ambidata – Digital Innovation Solutions & Consulting, Lda](https://www.g2.com/sellers/ambidata-digital-innovation-solutions-consulting-lda)
- **Year Founded:** 1999
- **HQ Location:** Vila Nova de Gaia, PT
- **Twitter:** @AmbidataLda  
54 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=b8bc07bdcb24dbebc599f44063508b9a94d3e7a4f89a634e3c28838047341fd4&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fambidatalda%2F&secure%5Burl_type%5D=linkedin_company_website)  
51 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 200% Large

### [NWA Quality Analyst](https://www.g2.com/products/nwa-quality-analyst/reviews)

NWA Quality Analyst® is an award winning SPC charting and analysis software solution providing the best combination of power, flexibility, and ease-of-use of any SPC software available. It enables a wide range of users to graphically analyze process behavior and judge the impact of process improvement decisions with minimal training in statistical techniques.

**Average Rating:** 4.5/5.0

**Total Reviews:** 1

#### Who Is the Company Behind NWA Quality Analyst?

- **Seller:** [Northwest Analytics](https://www.g2.com/sellers/northwest-analytics)
- **Year Founded:** 1980
- **HQ Location:** Portland, US
- **LinkedIn® Page:** [linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=d91534af91f9f1715e12a6a9484644321faeca64b040158c0e2a61f0ec2b5615&secure%5Burl%5D=https%3A%2F%2Flinkedin.com%2Fcompany%2Fnorthwest-analytics%2F&secure%5Burl_type%5D=linkedin_company_website)  
25 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Large

#### What Are Recent G2 Reviews of NWA Quality Analyst?

**["NWA for Finding Specified Process Capability"](https://www.g2.com/survey_responses/nwa-quality-analyst-review-2127213)**

**Rating:** 4.5/5.0 stars

_— Denzel Philip B._

[Read full review](https://www.g2.com/survey_responses/nwa-quality-analyst-review-2127213)

#### What Are G2 Users Discussing About NWA Quality Analyst?

- [What is NWA Quality Analyst used for?](https://www.g2.com/discussions/what-is-nwa-quality-analyst-used-for)

### [PRISYM SaaS](https://www.g2.com/products/prisym-saas/reviews)

PRISYM Medica is an enterprise labeling solution for medical device and life sciences organizations, specifically designed to meet international compliance requirements such as the FDA's labeling guidelines including 21CFR part 11.

**Average Rating:** 3.5/5.0

**Total Reviews:** 1

#### Who Is the Company Behind PRISYM SaaS?

- **Seller:** [PRISYM ID](https://www.g2.com/sellers/prisym-id)
- **HQ Location:** N/A
- **Twitter:** @LoftwareInc  
1,414 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=fcb865d309d30d15097aca4901dc94b44429d8a6e08c818b21f24e290c8d0bbe&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Floftware%2F&secure%5Burl_type%5D=linkedin_company_website)  
511 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Large

#### What Are G2 Users Discussing About PRISYM SaaS?

- [What is PRISYM SaaS used for?](https://www.g2.com/discussions/what-is-prisym-saas-used-for)

### [Qualitest Medical Devices & Life Sciences](https://www.g2.com/products/qualitest-group-qualitest-medical-devices-life-sciences/reviews)

Qualitest is the world's largest, independent managed services provider of quality assurance and testing solutions. QualiTest offers a wide range of healthcare testing services and medical software verification and validation services.

**Average Rating:** 5.0/5.0

**Total Reviews:** 1

#### How Do G2 Users Rate Qualitest Medical Devices & Life Sciences?

- **Has the product been a good partner in doing business?:** 10.0/10 (Category avg: 9.1/10)
- **Design Controls:** 8.3/10 (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 Qualitest Medical Devices & Life Sciences?

- **Seller:** [Qualitest Group](https://www.g2.com/sellers/qualitest-group)
- **Year Founded:** 1997
- **HQ Location:** London, England, United Kingdom
- **Twitter:** @QualiTest  
3,439 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=9b890279986f452c23cb341d26b9cab399c15022d0b6abb18737be8c4e3ebd20&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fqualitest&secure%5Burl_type%5D=linkedin_company_website)  
5,928 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Large

#### What Are Recent G2 Reviews of Qualitest Medical Devices & Life Sciences?

**["Medical Devices & Product Design"](https://www.g2.com/survey_responses/qualitest-medical-devices-life-sciences-review-8653403)**

**Rating:** 5.0/5.0 stars

_— Roshan S._

[Read full review](https://www.g2.com/survey_responses/qualitest-medical-devices-life-sciences-review-8653403)

### [SoftTrace](https://www.g2.com/products/softtrace/reviews)

SoftTrace LIMS provides a secure, configurable platform for full quality data management and traceability across the enterprise from raw materials to shipped product. It fast tracks reporting and enhances quality control processes throughout.

**Average Rating:** 4.0/5.0

**Total Reviews:** 1

#### Who Is the Company Behind SoftTrace?

- **Seller:** [SoftTrace](https://www.g2.com/sellers/softtrace)
- **Year Founded:** 2002
- **HQ Location:** Carrigtwohill, IE
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=aa02415c0d567dcc6340ccbe3d88ae7befb1b18333a813f2ac40163353dc63e0&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsofttrace-ltd%2F&secure%5Burl_type%5D=linkedin_company_website)  
15 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Large

#### What Are Recent G2 Reviews of SoftTrace?

**["A good kind experienxce"](https://www.g2.com/survey_responses/softtrace-review-498941)**

**Rating:** 4.0/5.0 stars

_— Verified User in Hospital & Health Care_

[Read full review](https://www.g2.com/survey_responses/softtrace-review-498941)

#### What Are G2 Users Discussing About SoftTrace?

- [What is SoftTrace used for?](https://www.g2.com/discussions/softtrace-what-is-softtrace-used-for)
- [What is SoftTrace used for?](https://www.g2.com/discussions/what-is-softtrace-used-for)

### [uniPoint](https://www.g2.com/products/unipoint/reviews)

Our configure-to-order Quality Management Software solution is designed to help your company automate its journey toward excellence. With twenty-five integrated software modules for quality and compliance management, uniPoint has transformed the quality management systems of 2,000+ Companies into a collaborative and paperless environment for continual improvement, while tracking the total administrative cost of quality at every stage. uniPoint uses the latest technology and offers a powerful feature set with unmatched simplicity and ease-of use.

**Average Rating:** 3.8/5.0

**Total Reviews:** 2

#### Who Is the Company Behind uniPoint?

- **Seller:** [uniPoint Software](https://www.g2.com/sellers/unipoint-software)
- **Year Founded:** 1996
- **HQ Location:** Winnipeg, CA
- **Twitter:** @uniPointnews  
10 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=63acf928e3c47a4b8056bf08868037f3c33df8a71a0427359f4dea286b89eaed&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Funipoint-software-inc%2F&secure%5Burl_type%5D=linkedin_company_website)  
18 employees on LinkedIn®

#### Who Uses This Product?

- **Company Size:** 100% Medium

#### What Are Recent G2 Reviews of uniPoint?

**["After using uniPoint for awhile, it is an easy software"](https://www.g2.com/survey_responses/unipoint-review-7116369)**

**Rating:** 4.0/5.0 stars

_— Verified User in Automotive_

[Read full review](https://www.g2.com/survey_responses/unipoint-review-7116369)

#### What Are G2 Users Discussing About uniPoint?

- [What is uniPoint used for?](https://www.g2.com/discussions/what-is-unipoint-used-for)

### [Adents VRS](https://www.g2.com/products/adents-vrs/reviews)

VRS is an interoperable solution used to manage the acceptance, formatting and delivery of the verification requests and responses. The built in look-up directory (LD) enables the proper routing of the verification requests and is synchronized across the VRS ecosystem.

#### Who Is the Company Behind Adents VRS?

- **Seller:** [Adents](https://www.g2.com/sellers/adents)
- **HQ Location:** Travagliato, IT
- **Twitter:** @Adentsinfo  
432 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=2a0b3e67289e54702d4ecf8e287168714977bb3243ace58e2bd0777563fb3f6b&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fantares-vision-group&secure%5Burl_type%5D=linkedin_company_website)  
939 employees on LinkedIn®

### [Advantum](https://www.g2.com/products/uc-ab-advantum/reviews)

Advantum Quality documentation is a quality management software that makes the management of quality documentation more effective and also compliant to regulations and specific industry standards.

#### Who Is the Company Behind Advantum?

- **Seller:** [UC AB](https://www.g2.com/sellers/uc-ab-65cdb97a-e530-416d-94e0-65b826ecb8e8)
- **Year Founded:** 1977
- **HQ Location:** Stockholm, SE
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=48f82b741c29df1655f10aefc3c69c2fea15c259cf6bc69361a440a52446aaec&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fuc-ab&secure%5Burl_type%5D=linkedin_company_website)  
241 employees on LinkedIn®

### [Agatha Quality](https://www.g2.com/products/agatha-quality/reviews)

Effectively managing clinical, compliance, and quality processes is a mission-critical task at life sciences companies. Quality improvements accelerate and improve processes, while quality failures can result in huge costs and disruptions. Choosing the right solution to track quality processes is a critical decision. Agatha Quality is a complete, ready-to-use application for capturing deviations, documenting corrective and preventive actions (CAPAs), and managing change control processes. Every action is connected, from the initial issue to the new process, and every step is documented, reviewed, and approved. More than document management, Agatha Quality is an end-to-end quality management system. Combining forms, documents, and workflows, Agatha Quality is a complete toolset for quality managers, pre-configured and validated but easy to adapt to specific process requirements Benefits - An End-to-End Process - A complete, closed-loop process captured in an expanding form, from initial issue to preventative action. A Complete QMS - Capture deviations, CAPAs, change controls, and audit activities to cover every part of the quality process. Inspection-Ready - Create complete quality records with electronic signatures, recorded approvals, and audit trails, all ready for inspection. Full Compliance - A validated system that is compliant with GxP requirements, EU Regulations, and FDA 21 CFR Part 11. Key Capabilities - Complete Metrics and Reporting - Get all the reporting you need with built-in dashboards and reports, and export reports for external reporting requirements. - Cross Workspace Reporting - Create views and reports across workspaces and export results to Excel for dashboard reports. Advanced Forms - Work with ready-to-use standard forms and processes, or adapt them to support your needs. Forms include rich text fields that allow the addition of images and formatted text. Use the form designer to update the look and feel of your forms. - A single multi-part form supports all steps in a process from deviation to change control. Reviews, approvals, and assignments for actions are also built-in. Preview, Edit, and Annotate - Review and edit Word, Excel, and PowerPoint documents directly in the application (does not require an Office license). - Annotate PDF, Office documents, and images with a simultaneous review of documents. Complete Records - Get complete quality records with signatures and audit trails, ready for inspection. Agatha QMS is fully compliant with 21 CFR Part 11 and EU regulatory requirements. - Agatha’s quality management application is also fully integrated with other Agatha applications making it easy to create references between them (eg. A CAPA can reference an SOP). More Than an Online Record - QMS forms are built on a Word template. When the form is converted to PDF, it’s more than a simple screenshot of the form on the page. Instead, you get a signed electronic record that is a nicely formatted PDF. Also Advanced Integration Toolkit - Use Agatha’s Rest API to allow applications to upload or export items from Agatha (includes documentation & sample code). Advanced Policy And Access Management - Manage policies, associated roles, and access controls easily. Secure Cloud - Agatha Applications are cloud-based, hosted in Agatha’s highly secure, highly reliant, high-performance, compliant, cloud environment. Three Editions: Standard, Extended, and Premium Some features are only available in Extended or Premium editions.

#### Who Is the Company Behind Agatha Quality?

- **Seller:** [Agatha](https://www.g2.com/sellers/agatha)
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=4dbc2fb4474bdb02e9acc94c4a3beed505ab79ec89f19894ddcb82d4ee97cb7d&secure%5Burl%5D=http%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fagatha-bijoux&secure%5Burl_type%5D=linkedin_company_website)  
5 employees on LinkedIn®

### [Agatha SOP](https://www.g2.com/products/agatha-sop/reviews)

Standard Operating Procedures (SOPs) and employee training documents are crucial to effective business operations, ensuring compliance with regulatory requirements during clinical trials. Managing both SOPs and employee records in one application simplifies the process and enhances overall job performance. This is where Agatha’s SOP management software comes into play. Initiate with Standard Operating Procedure (SOP) templates Review, approve and operate SOPs with clinical SOP management Monitor SOP compliance with clinical SOP management Controlled print – Clinical SOP management for paper copies

#### Who Is the Company Behind Agatha SOP?

- **Seller:** [Agatha](https://www.g2.com/sellers/agatha)
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=4dbc2fb4474bdb02e9acc94c4a3beed505ab79ec89f19894ddcb82d4ee97cb7d&secure%5Burl%5D=http%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fagatha-bijoux&secure%5Burl_type%5D=linkedin_company_website)  
5 employees on LinkedIn®

### [AlisQI](https://www.g2.com/products/alisqi/reviews)

AlisQI is a quality management platform built for mid-sized process and batch manufacturers. It helps manufacturers reduce recurring quality issues, improve operational control, and stay compliant by connecting quality, laboratory, and production data in a single source of truth. With AlisQI Solvers, organizations can start with the quality challenge that matters most, standardize processes across production sites, and expand their quality management system over time without replacing what already works. Our transparent, site-based pricing includes unlimited users, making it practical to involve everyone from the shop floor to senior management. Every employee can access the system with their own account, helping manufacturers build a true culture of quality without licensing costs increasing as adoption grows. AlisQI was founded on the belief that quality management software should adapt to manufacturing, not force manufacturers to adapt to the software. For more than 20 years, we have focused on building a platform that supports complex production environments, evolving processes, and demanding compliance requirements without becoming difficult to maintain or dependent on ongoing consulting. Those principles continue to shape the platform today. AlisQI was designed as a cloud solution before SaaS became mainstream, built around operational data rather than documents, and gives quality and operations teams the flexibility to improve and adapt their processes within a controlled, governed environment instead of relying on custom development.

#### Who Is the Company Behind AlisQI?

- **Seller:** [AlisQI](https://www.g2.com/sellers/alisqi)
- **Company Website:** www.alisqi.com
- **Year Founded:** 2002
- **HQ Location:** Amstelveen, NL
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=e8076f5bb0b3126b83514c957b2bbb299c9d0a2b92a32936354d0175b95445f9&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Falisqi%2F&secure%5Burl_type%5D=linkedin_company_website)  
28 employees on LinkedIn®
- **Phone:** +1 845-393-2870

### [Almond](https://www.g2.com/products/almond/reviews)

Almond® is a tool for managing the development of medical devices, that can save up to 2 years in the design and development process of medical device products; all in a secure cloud environment.

#### Who Is the Company Behind Almond?

- **Seller:** [Almond QMS](https://www.g2.com/sellers/almond-qms)
- **Year Founded:** 2015
- **HQ Location:** Haifa, IL
- **Twitter:** @QmsAlmond  
1 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=ff8e5aeb17061502c13c463131e566338055b5e8356e29a613771200584c3694&secure%5Burl%5D=http%3A%2F%2Fwww.linkedin.com%2Fcompany%2Falmond-qms&secure%5Burl_type%5D=linkedin_company_website)  
5 employees on LinkedIn®

### [AQMed](https://www.g2.com/products/aqmed/reviews)

AQMed is committed to transforming medical diagnostics by integrating artificial intelligence (AI) with advanced sensing technologies. Their flagship product, CardiAQ™, is a state-of-the-art magnetocardiography (MCG) device designed to enhance the speed and accuracy of cardiovascular disease diagnosis—the leading cause of death worldwide. This portable, non-invasive device captures the heart's magnetic signals without radiation, utilizing Large Quantitative Models (LQMs) and high-performance sensors to provide physicians with a powerful tool for early detection and improved patient outcomes.

#### Who Is the Company Behind AQMed?

- **Seller:** [SandboxAQ](https://www.g2.com/sellers/sandboxaq)
- **Year Founded:** 2021
- **HQ Location:** New York, NY
- **Twitter:** @SandboxAQ  
4,591 Twitter followers
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=ac916547986228197ad9bfd607eac26121a517315edd37e05c0f8b43e1a783aa&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fsandboxaq&secure%5Burl_type%5D=linkedin_company_website)  
245 employees on LinkedIn®

### [ARMATURE](https://www.g2.com/products/armature/reviews)

ARMATURE is a quality management software that measures quality for manufacturers and organizations. It manages the end-to-end quality process, with tools for process management, audit management, CAPAs, and standards management.

#### Who Is the Company Behind ARMATURE?

- **Seller:** [ARMATURE](https://www.g2.com/sellers/armature)
- **Year Founded:** 2000
- **HQ Location:** Herndon, US
- **LinkedIn® Page:** [www.linkedin.com](https://www.g2.com/external_clickthroughs/record?secure%5Bsource_type%5D=product_profile&secure%5Btoken%5D=1eda3d7fad3e8997b495cdd7b33ad83297e685e359afd301f92f3603bef22969&secure%5Burl%5D=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Farmature-solutions-corporation%2F&secure%5Burl_type%5D=linkedin_company_website)  
18 employees on LinkedIn®

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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

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