--- description: Get detailed information about Matrix Requirements usability, features, price, benefits and disadvantages from verified user experiences. Read reviews and discover similar tools on Capterra United Arab Emirates. image: https://gdm-localsites-assets-gfprod.imgix.net/images/capterra/og_logo-e5a8c001ed0bd1bb922639230fcea71a.png?auto=format%2Cenhance%2Ccompress title: Matrix Requirements Price, Reviews & Ratings - Capterra United Arab Emirates 2026 --- Breadcrumb: [Home](/) > [Requirements Management Software](/directory/10018/requirements-management/software) > [Matrix Requirements](/software/143557/matrix-requirements-medical) # Matrix Requirements Canonical: https://www.capterra.ae/software/143557/matrix-requirements-medical Page: 1 / 2\ Next: [Next page](https://www.capterra.ae/software/143557/matrix-requirements-medical?page=2) > Flexible ALM \& QMS solution for Medical Devices. Streamline Requirements Management with full traceability and quality compliance. > > Verdict: Rated **4.7/5** by 7 users. Top-rated for **Likelihood to recommend**. ----- ## Overview ### Who Uses Matrix Requirements? Medical Devices, Software as/in a Medical Device, Medtech ## Quick Stats & Ratings | Metric | Rating | Detail | | **Overall** | **4.7/5** | 7 Reviews | | Ease of Use | 4.1/5 | Based on overall reviews | | Customer Support Software | 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**: $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 - Access Controls/Permissions - Alerts/Notifications - Archiving & Retention - Audit Management - Change Management Software - Collaboration Tools - Complaint Management Software - Compliance Management - Compliance Tracking - Corrective and Preventive Actions (CAPA) - Customizable Templates - Dashboard Software - Document Capture - Document Classification - Document Coding & Control - Document Management Software - Document Storage - Electronic Signature - File Sharing Software - Full Text Search - IT Risk Management - Incident Management Software - Monitoring - Nonconformance Tracking - Operational Risk Management - Prioritization - Project Management Software - Quality Control - Reporting & Statistics - Reporting/Analytics - Risk Analysis - Risk Assessment - Risk Management Software - Risk Scoring - Root Cause Analysis - Search/Filter - Task Management Software - Third-Party Integrations - Training Management - Vendor Management Software - Version Control - Workflow Management Software ## Integrations (5 total) - GitHub - GitLab - Jira - Slack - YouTrack ## Support Options - Email/Help Desk - FAQs/Forum - Knowledge Base Software - Phone Support - Chat ## Category - [Requirements Management Software](https://www.capterra.ae/directory/10018/requirements-management/software) ## Related Categories - [Requirements Management Software](https://www.capterra.ae/directory/10018/requirements-management/software) - [Application Lifecycle Management Software](https://www.capterra.ae/directory/30525/application-lifecycle-management/software) - [Quality Management Software](https://www.capterra.ae/directory/30099/quality-management/software) - [Corrective and Preventive Action Software](https://www.capterra.ae/directory/31343/corrective-and-preventive-action/software) - [Compliance Software](https://www.capterra.ae/directory/30110/compliance/software) ## Alternatives 1. [MasterControl Quality Excellence](https://www.capterra.ae/software/148577/mastercontrol) — 4.5/5 (526 reviews) 2. [KAWAK](https://www.capterra.ae/software/211071/kawak) — 4.6/5 (319 reviews) 3. [Qualio](https://www.capterra.ae/software/134050/quality-management-software) — 4.6/5 (128 reviews) 4. [Dot Compliance](https://www.capterra.ae/software/192574/dot-compliance) — 4.4/5 (76 reviews) 5. [Ideagen Quality Management](https://www.capterra.ae/software/155354/Ideagen-Quality-Management) — 4.5/5 (178 reviews) ## Reviews ### "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. -Easy E-Sign and documentation. -User Template module. -Customer support. ----- ### "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 \& 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. ----- ### "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. Ability to structure the data in a way that makes generating compliance documentation easy. 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. 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.capterra.ae/software/143557/matrix-requirements-medical?page=2) ## Links - [View on Capterra](https://www.capterra.ae/software/143557/matrix-requirements-medical) ## This page is available in the following languages | Locale | URL | | de | | | de-AT | | | de-CH | | | en | | | en-AE | | | en-AU | | | en-CA | | | en-GB | | | en-IE | | | en-IL | | | en-IN | | | en-NZ | | | en-SG | | | en-ZA | | | fr | | | fr-BE | | | fr-CA | | | fr-LU | | | nl | | | nl-BE | | ----- ## Structured Data