Global Medical Device Podcast powered by Greenlight Guru

416 Afleveringen

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

   Gepubliceerd: 10-11-2021
2. Setting the Record Straight on Usability & Human Factors

   Gepubliceerd: 3-11-2021
3. Project Management for Product Development of Medical Devices

   Gepubliceerd: 27-10-2021
4. Assessing the Global Regulatory Landscape

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

   Gepubliceerd: 13-10-2021
6. When to Throw the Least Burdensome Flag on FDA

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

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

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

   Gepubliceerd: 8-9-2021
10. Meet a Guru: Maryann Mitchell

    Gepubliceerd: 2-9-2021
11. Why Storytelling Matters for Medical Device Companies

    Gepubliceerd: 25-8-2021
12. A Breakthrough Device that Aims to Prevent Osteoporosis

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

    Gepubliceerd: 11-8-2021
14. eQMS in Academia: Practical Learning for Biomedical Engineering Students

    Gepubliceerd: 28-7-2021
15. Tips for Running Better Management Reviews

    Gepubliceerd: 19-7-2021
16. Meet a Guru: Ryan Behringer

    Gepubliceerd: 14-7-2021
17. Navigating the MedTech Cybersecurity Ecosystem

    Gepubliceerd: 13-7-2021
18. Managing Clinical Data Activities

    Gepubliceerd: 7-7-2021
19. Explaining the Role of Importer under EU MDR

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

    Gepubliceerd: 23-6-2021