---
title: Watch Webinar | Use related risk analysis & how it applies to medical device development
description: The highly regulated field of medical device development requires identifying and mitigating use-related risks effectively. Find out how in this webinar.
image: https://cdmo.sanner-group.com/hubfs/HF%20Study%203.jpg
---

[Skip to content](https://cdmo.sanner-group.com/use-related-risk-analysis-how-it-applies-to-medical-device-development#main-content)

[![Logo\_Sanner\_RGB\_A4.jpg](https://cdmo.sanner-group.com/hs-fs/hubfs/Logo_Sanner_RGB_A4.jpg.jpeg?width=150&height=45&name=Logo_Sanner_RGB_A4.jpg.jpeg)](https://sanner-group.com?hsLang=en)

- Industries
- Solutions
- Capabilities
- About
- Insights

Open main navigation

Close main navigation

- Industries
- Solutions
- Capabilities
- About
- Insights
- [CONTACT US](https://www.sanner-group.com/contact-us)

[CONTACT US](https://www.sanner-group.com/contact-us?hsLang=en)

![HF Study 3](https://cdmo.sanner-group.com/hs-fs/hubfs/HF%20Study%203.jpg?width=2000&height=1333&name=HF%20Study%203.jpg "HF Study 3")

WEBINAR

## Use related risk analysis & how it applies to medical device development

As the landscape of medical device regulations continues to evolve, it’s crucial to stay ahead of the curve when it comes to Use-Related Risk Analysis (URRA).

In this webinar recording, we discuss URRA fundamentals, integrating Human Factors Engineering (HFE) with URRA,  
up-to-date regulatory insights, practical strategies for identifying and mitigating use-related risks, and case studies of URRA in action to understand its practical application.

[linkedin-in icon](https://www.linkedin.com/company/sannergroup)

---

[![Sanner\_Logo\_mit\_Claim\_hoizontal.jpg](https://cdmo.sanner-group.com/hs-fs/hubfs/Sanner_Logo_mit_Claim_hoizontal.jpg.jpeg?width=375&height=50&name=Sanner_Logo_mit_Claim_hoizontal.jpg.jpeg "Sanner_Logo_mit_Claim_hoizontal.jpg")](https://cdmo.sanner-group.com/?hsLang=en)

Bertha-Benz-Str. 5, 64625 Bensheim, Germany

Copyright © 2026, Sanner GmbH