416 Episodo

  1. Biocompatibility Nuances and its Impact on Medical Devices

    Publicado: 7/11/2019

  2. How to Make De Novo a Viable Option for your Medical Device

    Publicado: 7/11/2019

  3. Greenlight Guru In the Classroom: A University's Real-world Approach

    Publicado: 7/11/2019

  4. EU MDR: Not All Doom and Gloom

    Publicado: 7/11/2019

  5. Integrating Human Factors into Design Controls to Improve Patient Outcomes

    Publicado: 7/11/2019

  6. Is Your Medical Device Company CAPA Happy?

    Publicado: 7/11/2019

  7. Looking at the Sunset of FDA's Alternative Summary Reporting Program

    Publicado: 7/11/2019

  8. Challenges with MedTech Innovation

    Publicado: 7/11/2019

  9. Design History File Ready Ideation: An Innovative Approach to Product Development

    Publicado: 7/11/2019

  10. Importance of Software Requirements in Product Development

    Publicado: 7/11/2019

  11. 4 Facts That May Surprise You About FDA

    Publicado: 7/11/2019

  12. How General Wellness Devices Have Opened a Pandora's Box of Confusion

    Publicado: 7/11/2019

  13. Regulating Artificial Intelligence and Machine Learning-based Software as a Medical Device

    Publicado: 7/11/2019

  14. Challenges with Pediatric Medical Devices

    Publicado: 7/11/2019

  15. When Should You Start a QMS?

    Publicado: 7/11/2019

  16. Right-sizing your QMS

    Publicado: 7/11/2019

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The Global Medical Device Podcast, powered by Greenlight Guru, is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.

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