Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. Complaint Handling with Medical Device Guru, Brittney McIver

   Publisert: 3.5.2023
2. Avoiding Potential Issues with your 510(k) Submission

   Publisert: 28.4.2023
3. Meet a Guru: Brittani Smith

   Publisert: 20.4.2023
4. Why Building Supplier Relationships Is So Important

   Publisert: 12.4.2023
5. Systematic Literature Review for EU MDR

   Publisert: 5.4.2023
6. Building Your Design Controls (and Pitfalls to Avoid)

   Publisert: 29.3.2023
7. Most Common Problems Found During FDA Inspections in 2022

   Publisert: 24.3.2023
8. V&V Activities from a Verification Engineer POV - How Hard Could It Be?

   Publisert: 16.3.2023
9. Understanding the 'Compliance Manager' Role

   Publisert: 9.3.2023
10. DHF vs. DMR vs. DHR: Understanding the Differences & How They Interact

    Publisert: 2.3.2023
11. How Communication Affects the Outcomes of Quality Activities

    Publisert: 23.2.2023
12. Part 2: The Theranos Loophole & Lab Developed Tests

    Publisert: 16.2.2023
13. Part 1: The Theranos Loophole & Lab Developed Tests

    Publisert: 10.2.2023
14. Implementing an eQMS after Switching from Paper

    Publisert: 2.2.2023
15. Essentials of Sterilization for Med Device Professionals

    Publisert: 26.1.2023
16. UDI: 101

    Publisert: 21.1.2023
17. Quality Myths and Lessons Learned

    Publisert: 19.1.2023
18. Determining User Needs for Your Medical Device

    Publisert: 14.1.2023
19. Fraud in the Healthcare Industry & the Role of Whistleblowers

    Publisert: 12.1.2023
20. Auditing the Auditor

    Publisert: 7.1.2023