Global Medical Device Podcast powered by Greenlight Guru

416 Episodes

1. What are the Top Compliance Issues Plaguing Medical Device Manufacturers?

   Published: 11/10/2021
2. Setting the Record Straight on Usability & Human Factors

   Published: 11/3/2021
3. Project Management for Product Development of Medical Devices

   Published: 10/27/2021
4. Assessing the Global Regulatory Landscape

   Published: 10/21/2021
5. Quality Insights from a 40+ Year Veteran of the Medical Device Industry

   Published: 10/13/2021
6. When to Throw the Least Burdensome Flag on FDA

   Published: 10/6/2021
7. Past, Present, Future State (and World) of Quality in the Medical Device Industry

   Published: 9/22/2021
8. Focusing on the Intent of the UDI Requirements from FDA's Final Guidance Doc

   Published: 9/16/2021
9. Addressing the 'Who, What, When' of Quality in the Medical Device Industry

   Published: 9/8/2021
10. Meet a Guru: Maryann Mitchell

    Published: 9/2/2021
11. Why Storytelling Matters for Medical Device Companies

    Published: 8/25/2021
12. A Breakthrough Device that Aims to Prevent Osteoporosis

    Published: 8/19/2021
13. Understanding FDA's New Intended Use Rule and its Implications

    Published: 8/11/2021
14. eQMS in Academia: Practical Learning for Biomedical Engineering Students

    Published: 7/28/2021
15. Tips for Running Better Management Reviews

    Published: 7/19/2021
16. Meet a Guru: Ryan Behringer

    Published: 7/14/2021
17. Navigating the MedTech Cybersecurity Ecosystem

    Published: 7/13/2021
18. Managing Clinical Data Activities

    Published: 7/7/2021
19. Explaining the Role of Importer under EU MDR

    Published: 7/1/2021
20. Preparing Your Pre-Submission with the Content FDA Wants to See

    Published: 6/23/2021