Global Medical Device Podcast powered by Greenlight Guru

416 Episodio

1. Understanding and Handling Different Types of Feedback

   Pubblicato: 14/01/2021
2. Measuring the Impact of AI/ML Technologies on the Current Medical Device Landscape

   Pubblicato: 07/01/2021
3. Post-Pandemic Readiness: Preparing for the Aftermath of COVID-19 on the Medical Device Industry

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

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

   Pubblicato: 09/12/2020
6. Why SaMD Companies Should be Leveraging Pre-Submissions to FDA

   Pubblicato: 02/12/2020
7. What Goes into Designing Devices for Military and Emergency Applications?

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

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

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

    Pubblicato: 04/11/2020
11. Meet a Guru: Erica Loring

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

    Pubblicato: 30/09/2020
13. Challenges related to Home Use Devices

    Pubblicato: 10/09/2020
14. Submitting a 510(k) using FDA's Safety and Performance Based Pathway

    Pubblicato: 02/09/2020
15. How Jon Speer Met His Most Frequent Guest: Mike Drues

    Pubblicato: 26/08/2020
16. Meet a Guru: Wade Schroeder

    Pubblicato: 19/08/2020
17. What are the Audit Etiquette Rules I Should be Following?

    Pubblicato: 12/08/2020
18. Meet a Guru: Tom Rish

    Pubblicato: 05/08/2020
19. Addressing Clinical Trial Challenges & Concerns during COVID-19

    Pubblicato: 29/07/2020
20. Protecting the Intellectual Property of your Medical Device Technology

    Pubblicato: 22/07/2020