Global Medical Device Podcast powered by Greenlight Guru

393 Jaksot

1. How Mindset Training Can Help Your Team Operate at Peak Performance

   Julkaistiin: 10.6.2021
2. Examining the HHS Proposal for Premarket Notification Exemptions

   Julkaistiin: 7.6.2021
3. Crash Course on Greenlight Guru Academy: How Medical Device Professionals Stay Ahead

   Julkaistiin: 2.6.2021
4. Building your Brand as a Medical Device Professional

   Julkaistiin: 31.5.2021
5. Understanding the Value of a Medical Device Guru

   Julkaistiin: 26.5.2021
6. Meet a Guru: Etienne Nichols

   Julkaistiin: 24.5.2021
7. Meet a Guru: Laura Court

   Julkaistiin: 19.5.2021
8. Regulatory Tips & Pointers from a Former FDA Reviewer

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

   Julkaistiin: 12.5.2021
10. Comparing FDA’s Breakthrough Devices Program & Safer Technologies Program

    Julkaistiin: 11.5.2021
11. Why is IVDR Causing Widespread Panic throughout the Medical Device Industry?

    Julkaistiin: 7.5.2021
12. Managing Business Risk as a Medical Device Company

    Julkaistiin: 3.5.2021
13. Waterfall vs. Agile: Battle of the Product Development Methodologies

    Julkaistiin: 28.4.2021
14. For the Love of Internal Auditing

    Julkaistiin: 27.4.2021
15. Similarities & Differences between In Vitro Diagnostic (IVD) Devices & Medical Devices

    Julkaistiin: 21.4.2021
16. Knowing vs. Doing as Medical Device Professionals

    Julkaistiin: 20.4.2021
17. Pivoting Operations to Meet PPE Demand during Pandemic

    Julkaistiin: 14.4.2021
18. Pros & Cons of Being a Physician turned MedTech Inventor

    Julkaistiin: 13.4.2021
19. 3 Systems of Risk for Medical Devices from FDA

    Julkaistiin: 8.4.2021
20. Quality Management for IVD Devices vs Medical Devices

    Julkaistiin: 5.4.2021