---
title: EU MDR general safety and performance requirements (GSPR) checklist
canonical: "https://www.qualio.com/resources/eu-mdr-gspr-checklist"
updatedDate: "2026-10-26T16:24:35.000Z"
description: "Download Qualio's EU MDR general safety and performance requirements (GSPR) checklist. A step-by-step checklist to help life sciences teams stay compliant and audit-ready."
---

## EU MDR general safety and performance requirements (GSPR) checklist

Meet the EU MDR's general safety and performance requirements for your medical device.

## Download our EU MDR general safety and performance requirements (GSPR) checklist to:

### Understand every requirement your business and device(s) must follow for EU-compliant medical device safety and performance

### Take controlled step-by-step action to get compliant

### Pinpoint gaps in your medical device quality management system and satisfy your EU notified body inspector

## What you'll get

### 4-part XLSX checklist

Access a comprehensive and ordered Excel checklist to work your way through your GSPR demands

### Itemized action points

From referencing documents in your Design History File (DHF) to ticking off device requirements, work your way through the checklist to plug gaps and maximize compliance

### Annex-specific requirements list

Understand the requirements by annex and chapter and build a comprehensive record of documentation to prove compliance to your inspector