416 Episodo

  1. What are the Top Compliance Issues Plaguing Medical Device Manufacturers?

    Publicado: 10/11/2021
  2. Setting the Record Straight on Usability & Human Factors

    Publicado: 3/11/2021
  3. Project Management for Product Development of Medical Devices

    Publicado: 27/10/2021
  4. Assessing the Global Regulatory Landscape

    Publicado: 21/10/2021
  5. Quality Insights from a 40+ Year Veteran of the Medical Device Industry

    Publicado: 13/10/2021
  6. When to Throw the Least Burdensome Flag on FDA

    Publicado: 6/10/2021
  7. Past, Present, Future State (and World) of Quality in the Medical Device Industry

    Publicado: 22/9/2021
  8. Focusing on the Intent of the UDI Requirements from FDA's Final Guidance Doc

    Publicado: 16/9/2021
  9. Addressing the 'Who, What, When' of Quality in the Medical Device Industry

    Publicado: 8/9/2021
  10. Meet a Guru: Maryann Mitchell

    Publicado: 2/9/2021
  11. Why Storytelling Matters for Medical Device Companies

    Publicado: 25/8/2021
  12. A Breakthrough Device that Aims to Prevent Osteoporosis

    Publicado: 19/8/2021
  13. Understanding FDA's New Intended Use Rule and its Implications

    Publicado: 11/8/2021
  14. eQMS in Academia: Practical Learning for Biomedical Engineering Students

    Publicado: 28/7/2021
  15. Tips for Running Better Management Reviews

    Publicado: 19/7/2021
  16. Meet a Guru: Ryan Behringer

    Publicado: 14/7/2021
  17. Navigating the MedTech Cybersecurity Ecosystem

    Publicado: 13/7/2021
  18. Managing Clinical Data Activities

    Publicado: 7/7/2021
  19. Explaining the Role of Importer under EU MDR

    Publicado: 1/7/2021
  20. Preparing Your Pre-Submission with the Content FDA Wants to See

    Publicado: 23/6/2021

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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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