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Maintaining Business Continuity in the Medical Device Industry during Brexit Uncertainty
Maintaining Business Continuity in the Medical Device Industry during Brexit Uncertainty


 
Our Price: $395.00

Product Code: WB-7285
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Product Info
 
    About the Product
    Includes 1 Hour Windows Media Video File and PowerPoint presentations for immediate download.

    The EU and the UK recently reached an agreement on the Brexit transitional period, where EU law will continue to apply in the UK during the 21 month conversion. While this development was welcomed by many healthcare authorities and companies who will conduct business during and after the transition period, ambiguity remains regarding the UK’s future alignment with the EU regulatory framework and regulatory authorities. A thorough update on Brexit provisions specific to UK device research, development and marketing will be valuable to all device companies operating in the UK.

    • Brexit updates and timelines for CE-marked devices

    • Defining new roles of key stakeholders:

    • Manufacturer

    • Authorized Representative

    • Notified Body

    • Transition strategies with key action items for planning

    • Brexit and the new EU Medical Devices Regulation


    Speakers:
    Eveline Van Keymeulen
    Counsel
    Allen & Overy LLP


    Jacqueline Bore
    Life Sciences PSL
    Allen & Overy LLP

    Participants that will find this webinar most beneficial will be those involved in medical device companies. Job titles of attendees that will be most applicable for this session will be:

    • Regulatory Affairs

    • Legal

    • Operations

    • Compliance



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