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Reg with MEG

Reg with MEG

By: MedEnvoy Global
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About this listen

 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
  • Regulatory News Recap | Key FDA Changes Medical Device Manufacturers Need to Know

    Regulatory News Recap | Key FDA Changes Medical Device Manufacturers Need to Know
    Mar 31 2026

    In this episode of Reg with Meg’s Weekly Regulatory Roundup, we break down FDA Recognition List Number 065 and what it means for medical device manufacturers.

    #fda #medicaldevices #riskmanagement

    Note: This episode was created and hosted with AI.
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    10 mins
  • COFEPRIS Medical Device Submission Mistakes to Avoid

    COFEPRIS Medical Device Submission Mistakes to Avoid
    Mar 27 2026

    Listen to our breakdown of the most common COFEPRIS submission pitfalls for medical device and IVD manufactures. Also learn also how to avoid delays when entering your device into the Mexico market.

    #cofepris #deviceregistration

    *Disclaimer: This episode was created with AI
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    14 mins
  • 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
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