Global Medical Device Podcast powered by Greenlight Guru

398 Episodes

1. Explaining the Role of Importer under EU MDR

   Published: 7/1/2021
2. Preparing Your Pre-Submission with the Content FDA Wants to See

   Published: 6/23/2021
3. How RADx Tech II Program is Fast-Tracking COVID-19 Technologies to Market in 2021

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

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

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

   Published: 6/10/2021
7. Examining the HHS Proposal for Premarket Notification Exemptions

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

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

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

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

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

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

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

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

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

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

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

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

    Published: 4/27/2021
20. Similarities & Differences between In Vitro Diagnostic (IVD) Devices & Medical Devices

    Published: 4/21/2021