Blog

  • 11 August 2022 ViSU

    China UDI Requirements

  • 11 July 2022 ViSU

    Medical Devices: Structured Content Authoring Saves Time & Reduces Cost

  • 5 May 2022 ViSU

    5 Challenges of Medical Device Content & Solutions

  • 19 September 2022 ViSU

    Regulatory Managers Increase Flexibility without Losing Productivity

  • 2 April 2021 ViSU

    Current Alternatives To EUDAMED

  • 25 September 2020 ViSU

    UDI & EUDAMED Explained under EU MDR

  • 11 February 2020 ViSU

    Most Common and Avoidable Mistakes While Adopting ISO 13485

  • 31 January 2020 ViSU

    Regulatory Data and Info Management for Med Device Success

  • 28 November 2019 ViSU

    Effective Regulatory Change Management with Reg Intel Equipped RIM Tech

  • 21 October 2019 ViSU

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

  • 13 March 2019 ViSU

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