Global Medical Device Podcast powered by Greenlight Guru

416 Episodes

1. How RADx Tech II Program is Fast-Tracking COVID-19 Technologies to Market in 2021

   Published: 6/21/2021
2. How New Training Partnership is Advancing Medical Device Knowledge & Professional Development

   Published: 6/16/2021
3. Top 3 Most Cited Issues in Medical Device Inspections from FDA FY2020

   Published: 6/14/2021
4. How Mindset Training Can Help Your Team Operate at Peak Performance

   Published: 6/9/2021
5. Examining the HHS Proposal for Premarket Notification Exemptions

   Published: 6/7/2021
6. Crash Course on Greenlight Guru Academy: How Medical Device Professionals Stay Ahead

   Published: 6/2/2021
7. Building your Brand as a Medical Device Professional

   Published: 5/31/2021
8. Understanding the Value of a Medical Device Guru

   Published: 5/26/2021
9. Meet a Guru: Etienne Nichols

   Published: 5/24/2021
10. Meet a Guru: Laura Court

    Published: 5/19/2021
11. Regulatory Tips & Pointers from a Former FDA Reviewer

    Published: 5/17/2021
12. Why Demand is so High for Regulatory & Quality Jobs (and should you take advantage?)

    Published: 5/12/2021
13. Comparing FDA’s Breakthrough Devices Program & Safer Technologies Program

    Published: 5/11/2021
14. Why is IVDR Causing Widespread Panic throughout the Medical Device Industry?

    Published: 5/7/2021
15. Managing Business Risk as a Medical Device Company

    Published: 5/3/2021
16. Waterfall vs. Agile: Battle of the Product Development Methodologies

    Published: 4/28/2021
17. For the Love of Internal Auditing

    Published: 4/26/2021
18. Similarities & Differences between In Vitro Diagnostic (IVD) Devices & Medical Devices

    Published: 4/21/2021
19. Knowing vs. Doing as Medical Device Professionals

    Published: 4/19/2021
20. Pivoting Operations to Meet PPE Demand during Pandemic

    Published: 4/14/2021