Global Medical Device Podcast powered by Greenlight Guru

398 Episodes

1. Complaint Handling with Medical Device Guru, Brittney McIver

   Published: 5/3/2023
2. Avoiding Potential Issues with your 510(k) Submission

   Published: 4/28/2023
3. Meet a Guru: Brittani Smith

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

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

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

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

   Published: 3/24/2023
8. V&V Activities from a Verification Engineer POV - How Hard Could It Be?

   Published: 3/16/2023
9. Understanding the 'Compliance Manager' Role

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

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

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

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

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

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

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

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

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

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

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

    Published: 1/7/2023