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    Preparing for EUDAMED: what medical device companies need to do now

    Practical guidance to help quality and regulatory teams prepare for EUDAMED.

    Agenda

    06:50
    Official rollout timeline and key transition dates

    13:35
    Actor maintenance responsibilities by role

    26:40
    Practical readiness checklist and sustained compliance cadence

    32:25
    Summary: EUDAMED post-registration data maintenance

    36:10
    Q&A

    With the phased rollout of EUDAMED approaching, many MedTech companies still lack clarity on what it is, who must register, and how to prepare. During this training Karandeep Badwal, Founder and Principal Consultant at QRA Medical, and Angel Buendía, Scilife’s Knowledge Manager, will provide you with  a clear, structured overview of EUDAMED and help quality and regulatory teams move from uncertainty to practical readiness. 

     

    You’ll learn how to:

    • Navigate the EUDAMED rollout timeline and what is going live first.

    • HIdentify the different actor roles and responsibilities within EUDAMED.

    • Prepare your organisation for actor registration and future module use.

    • Avoid common mistakes and delays seen during real EUDAMED registrations.