The healthcare industry is changing and we have the breadth of expertise to help you evolve with it.

Comprehensive service offerings at every point in the product life cycle.

RAMS®

A platform of digital products to improve, simplify and automate RA/QA activities

OPUS™

Emergo by UL's new human factors tool - provides training, tools, and resources.

Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools.

The latest industry news and insights from our global team.

RADAR : Market Access Newsletter

Stay informed with the most read RA/QA medical device newsletter.

TalkingPoints : Human Factors Newsletter

TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.

Learn from our experts through live events.

Our global consulting team works from 20+ offices on six continents.

分析医疗器械安全相关使用错误的剩余风险

在这份来自Emergo by UL的人因工程研究与设计团队的白皮书中，了解如何确定在人因工程确认测试中观察到的安全相关使用错误是否可接受。

Person holding a syringe

借助剩余风险分析，医疗器械和体外诊断器械制造商可将观察到的使用错误纳入其设计考量，并判断这些错误是否会对患者或自我给药用户构成不可接受的风险。本文解释如何将剩余风险分析纳入更大的人因工程流程，讨论潜在严重使用错误的假设示例，为进行剩余风险分析的团队提供理想实践，并给出如何应对各种分析结果的指导。

下载我们的白皮书

Residual risk analysis of user interaction problems

2.34 MB

下载

US_HFRD_Residual_Risk_Analysis.pdf

Related services and training courses

Person using a machine to check their blood sugar

医疗器械开发中的综合性人因工程分析

Drawing of a scale

Advanced Residual Risk Analysis

Icon of a clipboard with a check mark on it

Residual Risk Analysis Training

了解剩余风险分析如何改善医疗器械患者安全性

Please wait…

相关内容

Human Factors software

OPUS™

You are leaving the Emergo by UL website for an external site. Emergo by UL structures this activity to be distinct and separate from its conformity assessment bodies.