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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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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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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 useful tips and gain a greater understanding of how to evaluate or design instructional materials for your medical devices and systems.
This webinar offers an understanding of the importance of human factors engineering (HFE) and why it's an essential part of the robotic healthcare technology design process.
Learn how to build an MDR compliant clinical evaluation process, the minimum content requirements of the CEP and their implications, the criteria for equivalency and differences with Meddev 2.7/1 Rev. 4.
Our experts cover the overwhelming benefits of conducting early user research to establish user needs and preferences, leading to results that can directly lead to safe, effective and satisfying medical technologies.
Gain insights from our medical device clinical research team on the role of PMCF studies in MDR compliance and what it takes to conduct a PMCF study that should be acceptable to all stakeholders.
This process chart illustrates the MHRA approval process per device classification in the U.K. and is available for download in the Regulatory Affairs Management Suite (RAMS).
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