Канал: Matrix Requirements

CE Marking Explained: How do you apply for certification?

CE Marking Explained: How do you apply for certification?

What is ISO 9001? What are the key differences between ISO 9001 and ISO 13485? All you need to know!

What is ISO 9001? What are the key differences between ISO 9001 and ISO 13485? All you need to know!

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.

What is MatrixALM (Application Lifecycle Management)?

What is MatrixALM (Application Lifecycle Management)?

What is IEC 62304? Everything you need to know to ensure Software Safety.

What is IEC 62304? Everything you need to know to ensure Software Safety.

Preparing a Device Master Record (DMR): All you need to know!

Preparing a Device Master Record (DMR): 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

FDA Software Validation Documentation: All you need to know

FDA Software Validation Documentation: All you need to know

CAPAS: Zoom in on Root Cause Analysis and CAPA Effectiveness check

CAPAS: Zoom in on Root Cause Analysis and CAPA Effectiveness check

What is ISO 14971 and how will it impact my Medical Device company?

What is ISO 14971 and how will it impact my Medical Device company?

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

Bridging the Gap between Agile Methodologies & Compliance

Bridging the Gap between Agile Methodologies & Compliance

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

Pytheas Navigation & Matrix Requirements

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. Requirements Management & Quality Management for Medical Devices.

Matrix Requirements. Requirements Management & Quality Management for Medical Devices.

Matrix Requirements: 2022 Annual Offsite - Las Palmas, Spain

Matrix Requirements: 2022 Annual Offsite - Las Palmas, Spain

Matrix Requirements Webinar: What's new in version 2.3?

Matrix Requirements Webinar: What's new in version 2.3?

Branching & Merging

Branching & Merging

Matrix Requirements Webinar: QMS Training

Matrix Requirements Webinar: QMS Training

Matrix Requirements Webinar: QMS Document Templates

Matrix Requirements Webinar: QMS Document Templates

Matrix Requirements Webinar: QMS Processes, SOPs and Work instructions

Matrix Requirements Webinar: QMS Processes, SOPs and Work instructions

Matrix Requirements Webinar: QMS Review Approval Workflow

Matrix Requirements Webinar: QMS Review Approval Workflow

Matrix Requirements Webinar: Tool Validation

Matrix Requirements Webinar: Tool Validation

Matrix Requirements Webinar: Design Reviews

Matrix Requirements Webinar: Design Reviews

Matrix Requirements Webinar: What's new in version 2.2?

Matrix Requirements Webinar: What's new in version 2.2?

Matrix Requirements Webinar: Document Creation

Matrix Requirements Webinar: Document Creation

Matrix Requirements Training: Creating Categories

Matrix Requirements Training: Creating Categories

Matrix Requirements Webinar: ALM JIRA Integration

Matrix Requirements Webinar: ALM JIRA Integration

Matrix Requirements Webinar: ALM Test Management

Matrix Requirements Webinar: ALM Test Management

Matrix Requirements Webinar: ALM Risk Management

Matrix Requirements Webinar: ALM Risk Management

Matrix Requirements Webinar: ALM Requirement Management

Matrix Requirements Webinar: ALM Requirement Management

Matrix Requirements: MatrixQMS Introduction

Matrix Requirements: MatrixQMS Introduction

Matrix Requirements: MatrixALM Introduction

Matrix Requirements: MatrixALM Introduction

Matrix ALM/QMS 2.1 - Reviews With Labels

Matrix ALM/QMS 2.1 - Reviews With Labels

Matrix ALM/QMS 2.1 - Simple Review

Matrix ALM/QMS 2.1 - Simple Review

Matrix ALM/QMS 2.1 - Administration of Review Controls

Matrix ALM/QMS 2.1 - Administration of Review Controls

Matrix ALM/QMS 2.1 - MRQL searches

Matrix ALM/QMS 2.1 - MRQL searches

Matrix ALM/QMS 2.1 - Documents Based on Searches

Matrix ALM/QMS 2.1 - Documents Based on Searches

Matrix ALM/QMS 2.1 - Redlining and Timewarp

Matrix ALM/QMS 2.1 - Redlining and Timewarp

How to add TemplateID Doc Property to a DOC template

How to add TemplateID Doc Property to a DOC template

Test Reporting

Test Reporting

Test Cycles

Test Cycles

Outdated tests

Outdated tests

Test Creation Changes Approval

Test Creation Changes Approval

Automation

Automation

Traceability and Documents

Traceability and Documents