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Reg with MEG

Reg with MEG

By: MedEnvoy Global
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 Reg with MEG brings together industry experts to explore the ever-changing world of global medical device compliance. From EU MDR/IVDR and FDA pathways to regulatory importer obligations, Post Market Surveillance (PMS), and market access, we break down complex regulatory topics into clear, actionable conversations.MedEnvoy Global Economics
Episodes
  • New Zealand Medical Device Registration Explained

    New Zealand Medical Device Registration Explained
    Mar 24 2026

    In this episode, we break down New Zealand’s uniquely streamlined regulatory system, where most medical devices don’t require pre-market approval. Instead, manufacturers rely on a notification-based process through the WAND database.

    *Disclaimer: This episode was created with AI
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    15 mins
  • EUDAMED & swissdamed | Mandatory Registration for 2026

    EUDAMED & swissdamed | Mandatory Registration for 2026
    Mar 13 2026

    Re-listen to our webinar, where our regulatory consultant Brittany Dunning discussed the upcoming UDI registration obligations for both EUDAMED and Switzerland’s swissdamed system, highlighting what companies need to do now to prepare.

    #eudamed #swissdamed #webinar

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    44 mins
  • swissdamed 2026 Deadline | What Medical Device Manufacturers Should Know

    swissdamed 2026 Deadline | What Medical Device Manufacturers Should Know
    Mar 12 2026

    swissdamed is coming and the July 1, 2026 deadline will be here soon. Join MedEnvoy's regulatory expert Brittany Dunning as she breaks down everything medical device manufacturers need to know: CHRN registration, UDI device uploads, timelines, and common pitfalls.

    #swissdamed #chrnregistration #medicaldevice
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    14 mins
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