Matrix One

For companies looking to accelerate development of their innovative medical device technologies, the Matrix One platform is an easy-to-use, flexible, all-in-one software solution that: facilitates collaboration of employees on design control, and quality management to streamline medical device design, establish lean quality management, accelerate product certification and go-to-market, and maintain regulatory compliance.

Matrix Requirements is an EN ISO 13485:2016 and ISO/IEC 27001:2013 certified company.
Visit www.matrixreq.com for information.

Matrix Mind Demo Video

Matrix Mind Demo Video
Pytheas Navigation & Matrix Requirements

Pytheas Navigation & Matrix Requirements
Introducing MatrixReq software

Introducing MatrixReq software
Medical Device Product Teams are Always Audit-Ready with Matrix.

Medical Device Product Teams are Always Audit-Ready with Matrix.
Fast Track Your Medical Device Launch in US and EU with Matrix Requirements

Fast Track Your Medical Device Launch in US and EU with Matrix Requirements
Developing AI-Powered Medical Devices - Matrix Requirements Webinar

Developing AI-Powered Medical Devices - Matrix Requirements Webinar
How To Classify Your Medical Device: Decoding Regulatory Pathways

How To Classify Your Medical Device: Decoding Regulatory Pathways
What is MatrixQMS (Quality Management System)?

What is MatrixQMS (Quality Management System)?
What Is Requirements Management?

What Is Requirements Management?
IEC 62304: Become an expert in Software Testing. All you need to know.

IEC 62304: Become an expert in Software Testing. All you need to know.
High Risk AI under European AI Act: Must know strategies for Medical Device Companies

High Risk AI under European AI Act: Must know strategies for Medical Device Companies
CAPAS: Zoom in on Root Cause Analysis and CAPA Effectiveness check

CAPAS: Zoom in on Root Cause Analysis and CAPA Effectiveness check
Remain Agile within Medical Device Development

Remain Agile within Medical Device Development
Launch Medical Device to Market in the EU vs US

Launch Medical Device to Market in the EU vs US
AI Act in Medical Device Industry & Europe - Key Objectives & What you need to know.

AI Act in Medical Device Industry & Europe - Key Objectives & What you need to know.
How to Prepare a Medical Device 510k Submission for FDA

How to Prepare a Medical Device 510k Submission for FDA
What is 21 CFR Part 820? How does this impact your Medical Device in US.

What is 21 CFR Part 820? How does this impact your Medical Device in US.
Navigating Regulatory Affairs and Ensuring Compliance in a Medtech Startup

Navigating Regulatory Affairs and Ensuring Compliance in a Medtech Startup
How will the AI Act in Europe impact Medical Devices?

How will the AI Act in Europe impact Medical Devices?
Matrix 2.4 Latest Release

Matrix 2.4 Latest Release
What is ISO 13485?

What is ISO 13485?
Sivan Innovation & Matrix Requirements

Sivan Innovation & Matrix Requirements
[Old] Pytheas Navigation & Matrix Requirements

[Old] Pytheas Navigation & Matrix Requirements
SxMD Templates with Matrix Requirements

SxMD Templates with Matrix Requirements
Matrix Requirements Compose feature release

Matrix Requirements Compose feature release
MIETHKE & MATRIX

MIETHKE & MATRIX
Matrix Requirements: 2022 Annual Offsite - Las Palmas, Spain

Matrix Requirements: 2022 Annual Offsite - Las Palmas, Spain