Global Medical Device Podcast powered by Greenlight Guru

416 Episodes

1. Meet a Guru: Brittani Smith

   Published: 4/20/2023
2. Why Building Supplier Relationships Is So Important

   Published: 4/12/2023
3. Systematic Literature Review for EU MDR

   Published: 4/5/2023
4. Building Your Design Controls (and Pitfalls to Avoid)

   Published: 3/29/2023
5. Most Common Problems Found During FDA Inspections in 2022

   Published: 3/23/2023
6. V&V Activities from a Verification Engineer POV - How Hard Could It Be?

   Published: 3/15/2023
7. Understanding the 'Compliance Manager' Role

   Published: 3/9/2023
8. DHF vs. DMR vs. DHR: Understanding the Differences & How They Interact

   Published: 3/2/2023
9. How Communication Affects the Outcomes of Quality Activities

   Published: 2/23/2023
10. Part 2: The Theranos Loophole & Lab Developed Tests

    Published: 2/16/2023
11. Part 1: The Theranos Loophole & Lab Developed Tests

    Published: 2/10/2023
12. Implementing an eQMS after Switching from Paper

    Published: 2/2/2023
13. Essentials of Sterilization for Med Device Professionals

    Published: 1/26/2023
14. UDI: 101

    Published: 1/21/2023
15. Quality Myths and Lessons Learned

    Published: 1/19/2023
16. Determining User Needs for Your Medical Device

    Published: 1/14/2023
17. Fraud in the Healthcare Industry & the Role of Whistleblowers

    Published: 1/12/2023
18. Auditing the Auditor

    Published: 1/7/2023
19. What is MedTech Lifecycle Excellence?

    Published: 1/5/2023
20. The Best of Jon & Mike Through the Years

    Published: 12/29/2022