5 episodes

MDRChats is your go-to audio destination for simplifying the regulatory landscape for medical device professionals, supported by ChatMDR (https://chatmdr.eu/).
Information on the latest updates, insights, and guidance documents; all designed to keep you informed and ahead in your field.
Whether you're on your commute, taking a break, or just prefer listening over reading, MDRChats is designed to fit seamlessly into your day. Our episodes transform your available moments into productive insights on regulatory changes.

MDRChats-by ChatMDR ChatMDR

    • Business

MDRChats is your go-to audio destination for simplifying the regulatory landscape for medical device professionals, supported by ChatMDR (https://chatmdr.eu/).
Information on the latest updates, insights, and guidance documents; all designed to keep you informed and ahead in your field.
Whether you're on your commute, taking a break, or just prefer listening over reading, MDRChats is designed to fit seamlessly into your day. Our episodes transform your available moments into productive insights on regulatory changes.

    Risk-Based Statistical Sampling Plan

    Risk-Based Statistical Sampling Plan

    A risk-based statistical sampling plan for medical devices adjusts sample sizes and testing criteria according to the potential impact of failures, guided by historical data and risk assessments. This method efficiently ensures product safety by matching testing intensity to the severity of possible risks


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    Send in a voice message: https://podcasters.spotify.com/pod/show/dinalakayan/message

    • 9 min
    A Deep Dive into Medical Device Deadlines

    A Deep Dive into Medical Device Deadlines

    In this podcast, regulatory experts discuss the extended deadlines under the Medical Device Regulation (MDR), focusing on the transitional periods for various classes of medical devices.


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    Send in a voice message: https://podcasters.spotify.com/pod/show/dinalakayan/message

    • 6 min
    The Significance of the EU AI Act for Medical Devices

    The Significance of the EU AI Act for Medical Devices

    In this episode of MDR Chats, we delve into the intersection of artificial intelligence and medical device regulation under the new EU Artificial Intelligence Act.

    This episode is created by chatMDR.eu .

    The voices in this podcast are AI-generated.


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    Send in a voice message: https://podcasters.spotify.com/pod/show/dinalakayan/message

    • 4 min
    Person Responsible for Regulatory Compliance, PRRC

    Person Responsible for Regulatory Compliance, PRRC

    Better understanding of the PRRC's role, responsibilities, and operational considerations for manufacturers and other economic operators.

    The voices in this podcast are AI-generated.


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    Send in a voice message: https://podcasters.spotify.com/pod/show/dinalakayan/message

    • 5 min
    MDRChats | Official Trailer

    MDRChats | Official Trailer

    MDRChats is your go-to podcast for the latest insights and updates on Medical Device Regulation, tailored for those with busy schedules.

    Our episodes are designed to enhance your understanding of MDR, keeping you informed and ahead in a rapidly evolving field. Subscribe to MDR Chats and effortlessly learn more about Medical Device Regulation.


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    Send in a voice message: https://podcasters.spotify.com/pod/show/dinalakayan/message

    • 28 sec

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