Emergo by UL
Emergo by UL is a single resource for helping you access the largest and fastest growing medical device markets worldwide. We are ready to assist you with medical device and IVD market access, human factors research and design, cybersecurity, clinical research, and more.Regulatory Affairs Management Suite (RAMS) is Emergo by UL's platform of digital products designed to improve and simplify medical device RA/QA activities. Create a RAMS account to access market tools and resources, regulatory intelligence, and automated registration tracking.
Emergo by UL’s new cloud-based human factors engineering (HFE) platform, Optimal Product Usability Suite (OPUS™), leverages training, tools, templates, and regulatory guidance to help you stay ahead in your HFE activities.
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Medical Device Regulatory Market Access in Times of a National Emergency
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Explore medical device and IVD market access
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Discover Human Factors Research & Design at Emergo by UL
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Introduction to the UDI System in the USA
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Introduction to Medical Device Labeling Symbols
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What To Expect From Your Regulatory Representative
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How to Prepare for an FDA Inspection
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Overview of the USA FDA Classification Process
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Introduction to Clinical Evaluation Reports (CER) for Europe
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Malaysia 2015 Overview HB
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South Korea Medical Device Registration Chapter 1 - Overview
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Mexico Medical Device Registration Chapter 5 - Post-market
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