416 Afleveringen

  1. Meet a Guru: Brittani Smith

    Gepubliceerd: 20-4-2023

  2. Why Building Supplier Relationships Is So Important

    Gepubliceerd: 12-4-2023

  3. Systematic Literature Review for EU MDR

    Gepubliceerd: 5-4-2023

  4. Building Your Design Controls (and Pitfalls to Avoid)

    Gepubliceerd: 29-3-2023

  5. Most Common Problems Found During FDA Inspections in 2022

    Gepubliceerd: 23-3-2023

  6. V&V Activities from a Verification Engineer POV - How Hard Could It Be?

    Gepubliceerd: 15-3-2023

  7. Understanding the 'Compliance Manager' Role

    Gepubliceerd: 9-3-2023

  8. DHF vs. DMR vs. DHR: Understanding the Differences & How They Interact

    Gepubliceerd: 2-3-2023

  9. How Communication Affects the Outcomes of Quality Activities

    Gepubliceerd: 23-2-2023

  10. Part 2: The Theranos Loophole & Lab Developed Tests

    Gepubliceerd: 16-2-2023

  11. Part 1: The Theranos Loophole & Lab Developed Tests

    Gepubliceerd: 10-2-2023

  12. Implementing an eQMS after Switching from Paper

    Gepubliceerd: 2-2-2023

  13. Essentials of Sterilization for Med Device Professionals

    Gepubliceerd: 26-1-2023

  14. UDI: 101

    Gepubliceerd: 21-1-2023

  15. Quality Myths and Lessons Learned

    Gepubliceerd: 19-1-2023

  16. Determining User Needs for Your Medical Device

    Gepubliceerd: 14-1-2023

  17. Fraud in the Healthcare Industry & the Role of Whistleblowers

    Gepubliceerd: 12-1-2023

  18. Auditing the Auditor

    Gepubliceerd: 7-1-2023

  19. What is MedTech Lifecycle Excellence?

    Gepubliceerd: 5-1-2023

  20. The Best of Jon & Mike Through the Years

    Gepubliceerd: 29-12-2022

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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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