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    Deutschland, Berlin, Business, Office, Team im Meetingraum
    • Webinar
      Medical Devices

    Best Practice for PSURs

    This insightful webinar will be beneficial for those with medical device Post-market Surveillance responsibilities under EU MDR.

    Watch the Webinar View the Presentation

    Key takeaways and learning objectives

    • An understanding of how to ensure the PSUR meets requirements

    • Awareness of PMS/PMCF requirements which may result in Notified Body action

    • Tips for a smooth submission and evaluation of the PSUR by BSI

    Speakers

    Presenter information

    Jenifer Hannon - Post Market Surveillance Regulatory Lead

    Andrew Butler - Technical Team Manager - Orthopaedics and Dental

    Susan Partridge - Clinical Regulatory Lead
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