FDA Today - EUA & SaMD

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  • Опубліковано 22 вер 2022
  • MedTech’s global regulatory landscape has changed drastically over the last decade. Policies are evolving across the globe and more programs and processes are being introduced by regulatory authorities to support further innovation.
    The regulatory landscape impacts both product development activities and commercialization timelines.
    In this True Quality Summit Series, we’re taking a tour around the world and diving into the state of regulations, upcoming critical events, and what you can expect in the future.
    ★ KEY VIDEO TAKEAWAY★
    There are a lot of lingering questions surrounding the FDA. When is the EUA ending? How is the FDA handling SaMD? What other deadlines and conversations are happening? Tune into one of our most highly anticipated sessions to learn more.
    This presentation originally aired during the 2022 Global MedTech Regulatory Trends Virtual Summit.
    If you’d like to watch more related videos, browse through the full list of free replays from this track of the virtual summit event: • 2022 Global MedTech Re...
    Plus, download the slides for this presentation for free here:
    www.slideshare.net/greenlight...
    Are you looking for a MedTech Lifecycle Excellence (MLE) platform to help you bring safer medical devices to market faster with less risk? Take a quick tour of Greenlight Guru's MLE platform: www.greenlight.guru/medtech-l...
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    #GlobalMedTechSummit #MedicalDevice #QMS

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