Global Medical Device Podcast powered by Greenlight Guru

Podcast tekijän mukaan Greenlight Guru + Medical Device Entrepreneurs - Torstaisin

Torstaisin

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393 Jaksot

  1. Tips to Prepare for EU MDR and IVDR as Deadlines Draw Near

    Julkaistiin: 17.12.2020
  2. How will Emergency Use Authorization (EUA) during Pandemic Influence Future FDA Policy Changes?

    Julkaistiin: 9.12.2020
  3. Why SaMD Companies Should be Leveraging Pre-Submissions to FDA

    Julkaistiin: 2.12.2020
  4. What Goes into Designing Devices for Military and Emergency Applications?

    Julkaistiin: 26.11.2020
  5. Are you Spending Enough Time Defining and Managing Requirements for your Medical Device?

    Julkaistiin: 19.11.2020
  6. Positive and Negative Impacts of EUA on the Medical Device Industry

    Julkaistiin: 12.11.2020
  7. Why Biocompatibility Should be Addressed by Every Medical Device Company

    Julkaistiin: 4.11.2020
  8. Meet a Guru: Erica Loring

    Julkaistiin: 28.10.2020
  9. What is a Multiple Function Device?

    Julkaistiin: 30.9.2020
  10. Challenges related to Home Use Devices

    Julkaistiin: 10.9.2020
  11. Submitting a 510(k) using FDA's Safety and Performance Based Pathway

    Julkaistiin: 2.9.2020
  12. How Jon Speer Met His Most Frequent Guest: Mike Drues

    Julkaistiin: 26.8.2020
  13. Meet a Guru: Wade Schroeder

    Julkaistiin: 20.8.2020
  14. What are the Audit Etiquette Rules I Should be Following?

    Julkaistiin: 12.8.2020
  15. Meet a Guru: Tom Rish

    Julkaistiin: 5.8.2020
  16. Addressing Clinical Trial Challenges & Concerns during COVID-19

    Julkaistiin: 29.7.2020
  17. Protecting the Intellectual Property of your Medical Device Technology

    Julkaistiin: 22.7.2020
  18. Meet a GURU: Jesseca Lyons

    Julkaistiin: 15.7.2020
  19. How to Build a QMS for a Medical Device

    Julkaistiin: 8.7.2020
  20. Meet a Guru: Taylor Brown

    Julkaistiin: 1.7.2020

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