---
description: Review of Matrix Requirements Software: system overview, features, price and cost information. Get free demos and compare to similar programs on Software Advice Ireland.
image: https://gdm-localsites-assets-gfprod.imgix.net/images/software_advice/og_logo-55146305bbe7b450bea05c18e9be9c9a.png
title: Matrix Requirements | Reviews, Pricing & Demos - SoftwareAdvice IE
---

Breadcrumb: [Home](/) > [CAPA Management Software](/directory/4713/capa/software) > [Matrix Requirements](/software/336473/matrix-requirements-medical)

# Matrix Requirements

Canonical: https://www.softwareadvice.ie/software/336473/matrix-requirements-medical

Page: 1 / 2\
Next: [Next page](https://www.softwareadvice.ie/software/336473/matrix-requirements-medical?page=2)

> Spend your time building Medical Devices, not on paperwork\!&#10;&#10;https://matrixreq.com/&#10;&#10;Matrix Requirements is helping medical device companies to easily and efficiently manage their design and quality system.&#10;Our products make your life easier by managing your medical device requirements, specifications, risks and tests ensuring full traceability and making sure you comply with all the regulations for your quality system.&#10;Matrix Requirements GmbH is ISO 13485 and ISO 27001 certified.&#10;&#10;MatrixALM - Application Lifecycle Management for medical devices:&#10;Our ALM solution helps your team build medical devices with less stress.&#10;Instead of writing big Word documents and trying to maintain Excel files for traceability and risks, MatrixALM allows you to update user and system requirements. Also technical specifications, tests, test results, risks and everything else you need to document for your design, can be created in an agile way.&#10;Let your whole team participate and benefit from up-to-date documentation\!&#10;This product offers you a leaner and more efficient design processes, a requirement, risk, test and change management with full traceability, a complete design history file of your product and more time to focus on building your medical device.&#10;&#10;MatrixQMS - Quality Management System for medical devices:&#10;Our QMS solution helps your team build a great quality system.&#10;MatrixQMS helps you to bridge the gap between the engineering teams and the quality department. It allows your RA/QA consultants to focus on the important things\!&#10;This product offers you a lean quality management system, a traceability from regulatory requirements to processes and work instructions with automated gap analysis, a support for your quality manual for ce marking and/or fda clearance and a process management with risk analysis integration.&#10;&#10;&#10;Our benefits:&#10;&#10;Matrix Requirements focus solely on medical devices and have a knowledgeable team of medical device engineers who can offer you quick and efficient online support. Matrix Requirements GmbH is ISO 13485 and ISO 27001 certified. And the team is composed of medical device engineers with offices in Belgium, Germany, France, US, and so on.&#10;We support large multi nationals as well as startups. A free setup and configuration support is also offered to fit your processes. &#10;&#10;Our lean applications are highly customizable to fit all your needs. Plus, as a dynamic and growing company we adjust our products continuously with the needs of your markets.&#10;&#10;You can connect Matrix with your favorite tools: Github, Gitlab, Broadcom Rally, Phabricator, Slack, Jira, YouTrack and so on.&#10;&#10;Matrix Requirements give access to the design to the whole team through a simple and online solution gives a higher visibility to the team and frees up the managers’ time leading to better products in less time.&#10;&#10;It unleashes the knowledge of your QA experts removing the need to do low skill documentation tasks.&#10;&#10;Matrix makes also paperless projects and processes bring efficiency, security and business velocity.&#10;&#10;Besides, the software ensure certification success through consistent and compliant documentation.&#10;&#10;Many features are available on our software such as Requirements Management, Risk Module, Test Module, Traceability, Predefined or Customizable Project Templates, Hierarchical Data Structure, Live Traceability Verification, File Attachments, Full, Session Comments, Project Analysis Reports, Controlled Documents, Document Templates, Electronic Signatures, JIRA Clouds Plug-in, Project Templates and much more.&#10;&#10;Come visit us on ou website: https://matrixreq.com/&#10;Want to know more about it, register for a demo with us (in English, French, German or Dutch): https://matrixreq.com/&#10;Or try it for free: https://matrixreq.com/\#sign-up-modal
> 
> Verdict: Rated **4.7/5** by 7 users. Top-rated for **Likelihood to recommend**.

-----

## Quick Stats & Ratings

| Metric | Rating | Detail |
| **Overall** | **4.7/5** | 7 Reviews |
| Ease of Use | 4.1/5 | Based on overall reviews |
| Customer Support | 5.0/5 | Based on overall reviews |
| Value for Money | 4.2/5 | Based on overall reviews |
| Features | 4.1/5 | Based on overall reviews |
| Recommendation percentage | 90% | (9/10 Likelihood to recommend) |

## About the vendor

- **Company**: Matrix One
- **Location**: Oberkirch, Germany
- **Founded**: 2014

## Commercial Context

- **Starting Price**: US$470.00
- **Pricing model**: Per User (Free Trial)
- **Pricing Details**: It is also available at $700/mo and $1050/mo with additional features.
- **Target Audience**: 2–10, 11–50, 51–200, 201–500, 501–1,000, 1,001–5,000, 5,001–10,000, 10,000+
- **Deployment & Platforms**: Cloud, SaaS, Web-based, Mac (Desktop), Windows (Desktop), Windows (On-Premise)
- **Supported Languages**: Danish, Dutch, English, Finnish, French, German, Italian
- **Available Countries**: Australia, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Israel, Italy, Luxembourg, Netherlands, New Zealand, Spain, Sweden, Switzerland, United Kingdom, United States

## Features

- @mentions
- API
- Access Controls/Permissions
- Activity Dashboard
- Activity Tracking
- Administrator Level Control
- Agile Methodologies
- Alerts/Notifications
- Application Management
- Approval Process Control
- Archiving & Retention
- Assessment Management
- Audit Management
- Audit Trail
- Automatic Test Generation
- Baseline Manager
- Bug Tracking
- Canned Responses
- Change Management
- Collaboration Tools

## Integrations (5 total)

- GitHub
- GitLab
- Jira
- Slack
- YouTrack

## Support Options

- Email/Help Desk
- FAQs/Forum
- Knowledge Base
- Phone Support
- Chat

## Category

- [CAPA Management Software](https://www.softwareadvice.ie/directory/4713/capa/software)

## Related Categories

- [CAPA Management Software](https://www.softwareadvice.ie/directory/4713/capa/software)
- [Complaint Management Software](https://www.softwareadvice.ie/directory/499/complaint-management/software)
- [Compliance Software](https://www.softwareadvice.ie/directory/4363/compliance/software)
- [Quality Management Software](https://www.softwareadvice.ie/directory/420/quality-management-software/software)
- [Integrated Risk Management Software](https://www.softwareadvice.ie/directory/4101/integrated-risk-management/software)

## Alternatives

1. [MasterControl Quality Excellence](https://www.softwareadvice.ie/software/142000/mastercontrol) — 4.5/5 (526 reviews)
2. [KAWAK](https://www.softwareadvice.ie/software/357377/kawak) — 4.6/5 (319 reviews)
3. [Qualio](https://www.softwareadvice.ie/software/152557/qualio) — 4.6/5 (128 reviews)
4. [Isolocity](https://www.softwareadvice.ie/software/79422/isolocity) — 4.7/5 (51 reviews)
5. [Dot Compliance](https://www.softwareadvice.ie/software/239986/dot-compliance) — 4.4/5 (76 reviews)

## Reviews

### "Very useful for Planning from SRSs till Formal verification" — 5.0/5

> **Verified Reviewer** | *5 December 2022* | Information Technology & Services | Recommendation rating: 9.0/10
> 
> **Pros**: The thing i like most about is the links(Up \&amp; down) that can be given to a specific items
> 
> **Cons**: The ability of creating new type of documents is limited to Administrator. A little bit more exposure to more admin abilities can be given to users to be able to create new type of documents to make their work easier and increase effective performance.
> 
> The overall experience was very satisfactory.

-----

### "MM tool all medical device development company need." — 5.0/5

> **Sunil Kumar** | *23 February 2025* | Hospital & Health Care | Recommendation rating: 8.0/10
> 
> **Pros**: MM is a very thoughtfully designed product.
> 
> **Cons**: -Simple workflow.&#10;-Easy E-Sign and documentation.&#10;-User Template module.&#10;-Customer support.

-----

### "Great software for agile software development\!" — 4.0/5

> **Karen** | *23 September 2017*
> 
> **Pros**: Built in risk analysis module, easy creation of technical documents, traceability , report section and link with jira
> 
> **Cons**: Bad layouts of downloaded documents. Not possible to search in sign section and need to download the doc Each time you want to read it. Not user friendly for writing document regarding layout stuff, tables, for each project do user settings manually, a lot of work when a user leaves the rcompany, manually organising sign documents in folder, no cross project interactions

-----

### "It was easy to get started andI am continuing to discover the many great features of this software." — 5.0/5

> **Geetha** | *25 September 2017* | Medical Devices | Recommendation rating: 10.0/10
> 
> **Pros**: I truly appreciate the flexibility and configurability of the functions. But more than that, I appreciate the technical support that is always prompt and very helpful.
> 
> **Cons**: The user interface is not always easy to follow. Also unfortunately, many of the best features are too hidden.
> 
> Convenient way to maintain design data.&#13;&#10;Ability to structure the data in a way that makes generating compliance documentation easy.&#13;&#10;Ability to collaborate across geographies and have multiple people work on design content

-----

### "The system provides a means to create structure and relations between technical documentation." — 4.0/5

> **Thijs** | *25 September 2017* | Medical Devices | Recommendation rating: 8.0/10
> 
> **Pros**: The ability to work together within a team to create requirements and specifications, create documents from those requirements and specifications and continuously keep a clear overview of the relation between those components, as well as their relation to the identified risks and design outputs.&#13;&#10;&#13;&#10;The support for using the software and to discuss possible (new) features is very good with a short response time with clear information every single time.
> 
> **Cons**: The overall design and layout of the system could be improved from an aesthetic and intuitiveness point.

-----

Page: 1 / 2\
Next: [Next page](https://www.softwareadvice.ie/software/336473/matrix-requirements-medical?page=2)

## Links

- [View on SoftwareAdvice](https://www.softwareadvice.ie/software/336473/matrix-requirements-medical)

## This page is available in the following languages

| Locale | URL |
| de | <https://www.softwareadvice.de/software/336473/matrix-requirements-medical> |
| en | <https://www.softwareadvice.com/crm/matrix-requirements-medical-profile/> |
| en-AU | <https://www.softwareadvice.com.au/software/336473/matrix-requirements-medical> |
| en-GB | <https://www.softwareadvice.co.uk/software/336473/matrix-requirements-medical> |
| en-IE | <https://www.softwareadvice.ie/software/336473/matrix-requirements-medical> |
| en-NZ | <https://www.softwareadvice.co.nz/software/336473/matrix-requirements-medical> |
| fr | <https://www.softwareadvice.fr/software/336473/matrix-requirements-medical> |

-----

## Structured Data

<script type="application/ld+json">
  {"@context":"https://schema.org","@graph":[{"name":"SoftwareAdvice Ireland","address":{"@type":"PostalAddress","addressLocality":"Dublin","addressRegion":"D","postalCode":"D02 NP94","streetAddress":"2 Park Place, 3rd Floor, Hatch St Dublin, D02 NP94 Ireland"},"description":"We've helped more than 500000 buyers to find the right software.","email":"info@softwareadvice.ie","url":"https://www.softwareadvice.ie/","logo":"https://dm-localsites-assets-prod.imgix.net/images/software_advice/logo-white-d2cfd05bdd863947d19a4d1b9567dde8.svg","@type":"Organization","@id":"https://www.softwareadvice.ie/#organization","parentOrganization":"Gartner, Inc.","sameAs":[]},{"name":"Matrix Requirements","description":"Spend your time building Medical Devices, not on paperwork!\n\nhttps://matrixreq.com/\n\nMatrix Requirements is helping medical device companies to easily and efficiently manage their design and quality system.\nOur products make your life easier by managing your medical device requirements, specifications, risks and tests ensuring full traceability and making sure you comply with all the regulations for your quality system.\nMatrix Requirements GmbH is ISO 13485 and ISO 27001 certified.\n\nMatrixALM - Application Lifecycle Management for medical devices:\nOur ALM solution helps your team build medical devices with less stress.\nInstead of writing big Word documents and trying to maintain Excel files for traceability and risks, MatrixALM allows you to update user and system requirements. Also technical specifications, tests, test results, risks and everything else you need to document for your design, can be created in an agile way.\nLet your whole team participate and benefit from up-to-date documentation!\nThis product offers you a leaner and more efficient design processes, a requirement, risk, test and change management with full traceability, a complete design history file of your product and more time to focus on building your medical device.\n\nMatrixQMS - Quality Management System for medical devices:\nOur QMS solution helps your team build a great quality system.\nMatrixQMS helps you to bridge the gap between the engineering teams and the quality department. It allows your RA/QA consultants to focus on the important things!\nThis product offers you a lean quality management system, a traceability from regulatory requirements to processes and work instructions with automated gap analysis, a support for your quality manual for ce marking and/or fda clearance and a process management with risk analysis integration.\n\n\nOur benefits:\n\nMatrix Requirements focus solely on medical devices and have a knowledgeable team of medical device engineers who can offer you quick and efficient online support. Matrix Requirements GmbH is ISO 13485 and ISO 27001 certified. And the team is composed of medical device engineers with offices in Belgium, Germany, France, US, and so on.\nWe support large multi nationals as well as startups. A free setup and configuration support is also offered to fit your processes. \n\nOur lean applications are highly customizable to fit all your needs. Plus, as a dynamic and growing company we adjust our products continuously with the needs of your markets.\n\nYou can connect Matrix with your favorite tools: Github, Gitlab, Broadcom Rally, Phabricator, Slack, Jira, YouTrack and so on.\n\nMatrix Requirements give access to the design to the whole team through a simple and online solution gives a higher visibility to the team and frees up the managers’ time leading to better products in less time.\n\nIt unleashes the knowledge of your QA experts removing the need to do low skill documentation tasks.\n\nMatrix makes also paperless projects and processes bring efficiency, security and business velocity.\n\nBesides, the software ensure certification success through consistent and compliant documentation.\n\nMany features are available on our software such as Requirements Management, Risk Module, Test Module, Traceability, Predefined or Customizable Project Templates, Hierarchical Data Structure, Live Traceability Verification, File Attachments, Full, Session Comments, Project Analysis Reports, Controlled Documents, Document Templates, Electronic Signatures, JIRA Clouds Plug-in, Project Templates and much more.\n\nCome visit us on ou website: https://matrixreq.com/\nWant to know more about it, register for a demo with us (in English, French, German or Dutch): https://matrixreq.com/\nOr try it for free: https://matrixreq.com/#sign-up-modal","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductScreenshot/8b52d9a0-9773-4bd3-be26-d40c263eed02.png","url":"https://www.softwareadvice.ie/software/336473/matrix-requirements-medical","@type":"SoftwareApplication","@id":"https://www.softwareadvice.ie/software/336473/matrix-requirements-medical#software","applicationCategory":"BusinessApplication","publisher":{"@id":"https://www.softwareadvice.ie/#organization"},"aggregateRating":{"@type":"AggregateRating","ratingValue":4.7,"bestRating":5,"ratingCount":7},"offers":{"price":"470","@type":"Offer","priceCurrency":"USD"},"operatingSystem":"Cloud, Apple, Windows, Windows on premise"},{"@type":"BreadcrumbList","itemListElement":[{"name":"Home","position":1,"item":"/","@type":"ListItem"},{"name":"CAPA Management Software","position":2,"item":"/directory/4713/capa/software","@type":"ListItem"},{"name":"Matrix Requirements","position":3,"item":"/software/336473/matrix-requirements-medical","@type":"ListItem"}],"@id":"https://www.softwareadvice.ie/software/336473/matrix-requirements-medical#breadcrumblist"}]}
</script>
