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

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

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    Featured

    • South African regulators issue guidance for medical device imports, advertising

      Manufacturers must comply with latest rules

    • What will the UK MHRA consultation bring in terms of medical device and IVD regulations?

      Changes in store for medical device and IVD regulations in the UK

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    MDR Resource Center

    The knowledge you need for MDR implementation

    Europe's Medical Devices Regulation (MDR) goes into effect in May 2020, and we want you to be prepared. Meet our MDR team and get free educational resources on the MDR.

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    Upcoming

    • Designing safe and effective instructional materials for medical devices

      July 07, 2022

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© 2022 EMERGO by UL. All Rights Reserved. Privacy Terms of Use Data Subject Access Request Portal

Within the UL family of companies we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brands, UL is unable to provide consultancy services to Notified Body or MDSAP customers. UL has processes in place to identify and manage any potential conflicts of interest and maintain impartiality.