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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.
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Stay informed with the most read RA/QA medical device newsletter.
TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.
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Learn from our experts through live events.
Our global consulting team works from 20+ offices on six continents.
Our team of experts has compiled case studies, white papers, process charts, guides, eLearning courses, market data, videos and additional resources for your reference.
Learn more about taking a strategic approach to achieve regulatory approval in medical device markets around the world.
Meet the human factors engineering (HFE) expectations, regulations and standards of a global marketplace.
Watch our Emergo by UL subject matter expert as they outline the latest updates about US FDA electronic Submission Template and Resource (eSTAR).
This presentation, presented in Portuguese, reviews the resources of the European Commission.
Develop a greater understanding of the importance of incorporating human factors engineering (HFE) into post-market surveillance activities.
Our white paper explains the FDA’s risk-based classification system for medical devices.
In this webinar, our Emergo by UL expert outlines the latest updates on how the IVDR impacts intended purpose and classification.
Read this white paper to learn about FDA requirements for clinical evidence.
Regardez maintenant : le logiciel en tant que dispositif médical (SaMD) : considérations réglementaires UE/USA
In this webinar, our Emergo by UL subject matter expert outlines the latest updates about preparing for IVDR certification regulation updates.
Learn about EUDAMED database compliance requirements for medical device and in-vitro diagnostics (IVD) companies in Europe.
In this webinar, our Emergo by UL subject matter expert outlines the latest EU market regulatory updates.
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