Global Medical Device Podcast powered by Greenlight Guru

416 Odcinki

1. Understanding and Handling Different Types of Feedback

   Opublikowany: 14.01.2021
2. Measuring the Impact of AI/ML Technologies on the Current Medical Device Landscape

   Opublikowany: 7.01.2021
3. Post-Pandemic Readiness: Preparing for the Aftermath of COVID-19 on the Medical Device Industry

   Opublikowany: 23.12.2020
4. Tips to Prepare for EU MDR and IVDR as Deadlines Draw Near

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

   Opublikowany: 9.12.2020
6. Why SaMD Companies Should be Leveraging Pre-Submissions to FDA

   Opublikowany: 2.12.2020
7. What Goes into Designing Devices for Military and Emergency Applications?

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

   Opublikowany: 18.11.2020
9. Positive and Negative Impacts of EUA on the Medical Device Industry

   Opublikowany: 12.11.2020
10. Why Biocompatibility Should be Addressed by Every Medical Device Company

    Opublikowany: 4.11.2020
11. Meet a Guru: Erica Loring

    Opublikowany: 28.10.2020
12. What is a Multiple Function Device?

    Opublikowany: 30.09.2020
13. Challenges related to Home Use Devices

    Opublikowany: 10.09.2020
14. Submitting a 510(k) using FDA's Safety and Performance Based Pathway

    Opublikowany: 2.09.2020
15. How Jon Speer Met His Most Frequent Guest: Mike Drues

    Opublikowany: 26.08.2020
16. Meet a Guru: Wade Schroeder

    Opublikowany: 19.08.2020
17. What are the Audit Etiquette Rules I Should be Following?

    Opublikowany: 12.08.2020
18. Meet a Guru: Tom Rish

    Opublikowany: 5.08.2020
19. Addressing Clinical Trial Challenges & Concerns during COVID-19

    Opublikowany: 29.07.2020
20. Protecting the Intellectual Property of your Medical Device Technology

    Opublikowany: 22.07.2020