Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. Explaining the Role of Importer under EU MDR

   Publisert: 1.7.2021
2. Preparing Your Pre-Submission with the Content FDA Wants to See

   Publisert: 23.6.2021
3. How RADx Tech II Program is Fast-Tracking COVID-19 Technologies to Market in 2021

   Publisert: 21.6.2021
4. How New Training Partnership is Advancing Medical Device Knowledge & Professional Development

   Publisert: 16.6.2021
5. Top 3 Most Cited Issues in Medical Device Inspections from FDA FY2020

   Publisert: 14.6.2021
6. How Mindset Training Can Help Your Team Operate at Peak Performance

   Publisert: 10.6.2021
7. Examining the HHS Proposal for Premarket Notification Exemptions

   Publisert: 7.6.2021
8. Crash Course on Greenlight Guru Academy: How Medical Device Professionals Stay Ahead

   Publisert: 2.6.2021
9. Building your Brand as a Medical Device Professional

   Publisert: 31.5.2021
10. Understanding the Value of a Medical Device Guru

    Publisert: 26.5.2021
11. Meet a Guru: Etienne Nichols

    Publisert: 24.5.2021
12. Meet a Guru: Laura Court

    Publisert: 19.5.2021
13. Regulatory Tips & Pointers from a Former FDA Reviewer

    Publisert: 17.5.2021
14. Why Demand is so High for Regulatory & Quality Jobs (and should you take advantage?)

    Publisert: 12.5.2021
15. Comparing FDA’s Breakthrough Devices Program & Safer Technologies Program

    Publisert: 11.5.2021
16. Why is IVDR Causing Widespread Panic throughout the Medical Device Industry?

    Publisert: 7.5.2021
17. Managing Business Risk as a Medical Device Company

    Publisert: 3.5.2021
18. Waterfall vs. Agile: Battle of the Product Development Methodologies

    Publisert: 28.4.2021
19. For the Love of Internal Auditing

    Publisert: 27.4.2021
20. Similarities & Differences between In Vitro Diagnostic (IVD) Devices & Medical Devices

    Publisert: 21.4.2021