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    25 July 2023 ViSU

    EUDAMED Vigilance Requirements and Steps

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    7 June 2023 ViSU

    How Device Companies Can Drive Regulatory Digitization

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    15 May 2023 ViSU

    eIFU for Medical Devices: Country Specific Regulations and Benefits

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    18 April 2023 ViSU

    Singapore UDI Phase – 1 Implementation

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    17 February 2023 ViSU

    What EU MDR changes mean to Manufacturers & what’s Next !

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    11 August 2022 ViSU

    China UDI Requirements

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    11 July 2022 ViSU

    Medical Devices: Structured Content Authoring Saves Time & Reduces Cost

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    5 May 2022 ViSU

    5 Challenges of Medical Device Content & Solutions

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    19 September 2022 ViSU

    Regulatory Managers Increase Flexibility without Losing Productivity

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    2 April 2021 ViSU

    Current Alternatives To EUDAMED

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    25 September 2020 ViSU

    UDI & EUDAMED Explained under EU MDR

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    11 February 2020 ViSU

    Most Common and Avoidable Mistakes While Adopting ISO 13485

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    31 January 2020 ViSU

    Regulatory Data and Info Management for Med Device Success

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    28 November 2019 ViSU

    Effective Regulatory Change Management with Reg Intel Equipped RIM Tech

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    21 October 2019 ViSU

    Reg Information/Data for Devices, very important going forward!

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    13 March 2019 ViSU

    Digitize Instructions for Use (IFU) to Comply with EU MDR

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