Global Medical Device Podcast powered by Greenlight Guru

416 Episodo

1. Understanding and Handling Different Types of Feedback

   Publicado: 14/1/2021
2. Measuring the Impact of AI/ML Technologies on the Current Medical Device Landscape

   Publicado: 7/1/2021
3. Post-Pandemic Readiness: Preparing for the Aftermath of COVID-19 on the Medical Device Industry

   Publicado: 23/12/2020
4. Tips to Prepare for EU MDR and IVDR as Deadlines Draw Near

   Publicado: 17/12/2020
5. How will Emergency Use Authorization (EUA) during Pandemic Influence Future FDA Policy Changes?

   Publicado: 9/12/2020
6. Why SaMD Companies Should be Leveraging Pre-Submissions to FDA

   Publicado: 2/12/2020
7. What Goes into Designing Devices for Military and Emergency Applications?

   Publicado: 26/11/2020
8. Are you Spending Enough Time Defining and Managing Requirements for your Medical Device?

   Publicado: 18/11/2020
9. Positive and Negative Impacts of EUA on the Medical Device Industry

   Publicado: 12/11/2020
10. Why Biocompatibility Should be Addressed by Every Medical Device Company

    Publicado: 4/11/2020
11. Meet a Guru: Erica Loring

    Publicado: 28/10/2020
12. What is a Multiple Function Device?

    Publicado: 30/9/2020
13. Challenges related to Home Use Devices

    Publicado: 10/9/2020
14. Submitting a 510(k) using FDA's Safety and Performance Based Pathway

    Publicado: 2/9/2020
15. How Jon Speer Met His Most Frequent Guest: Mike Drues

    Publicado: 26/8/2020
16. Meet a Guru: Wade Schroeder

    Publicado: 19/8/2020
17. What are the Audit Etiquette Rules I Should be Following?

    Publicado: 12/8/2020
18. Meet a Guru: Tom Rish

    Publicado: 5/8/2020
19. Addressing Clinical Trial Challenges & Concerns during COVID-19

    Publicado: 29/7/2020
20. Protecting the Intellectual Property of your Medical Device Technology

    Publicado: 22/7/2020