Global Medical Device Podcast powered by Greenlight Guru

416 Odcinki

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

   Opublikowany: 10.11.2021
2. Setting the Record Straight on Usability & Human Factors

   Opublikowany: 3.11.2021
3. Project Management for Product Development of Medical Devices

   Opublikowany: 27.10.2021
4. Assessing the Global Regulatory Landscape

   Opublikowany: 21.10.2021
5. Quality Insights from a 40+ Year Veteran of the Medical Device Industry

   Opublikowany: 13.10.2021
6. When to Throw the Least Burdensome Flag on FDA

   Opublikowany: 6.10.2021
7. Past, Present, Future State (and World) of Quality in the Medical Device Industry

   Opublikowany: 22.09.2021
8. Focusing on the Intent of the UDI Requirements from FDA's Final Guidance Doc

   Opublikowany: 16.09.2021
9. Addressing the 'Who, What, When' of Quality in the Medical Device Industry

   Opublikowany: 8.09.2021
10. Meet a Guru: Maryann Mitchell

    Opublikowany: 2.09.2021
11. Why Storytelling Matters for Medical Device Companies

    Opublikowany: 25.08.2021
12. A Breakthrough Device that Aims to Prevent Osteoporosis

    Opublikowany: 19.08.2021
13. Understanding FDA's New Intended Use Rule and its Implications

    Opublikowany: 11.08.2021
14. eQMS in Academia: Practical Learning for Biomedical Engineering Students

    Opublikowany: 28.07.2021
15. Tips for Running Better Management Reviews

    Opublikowany: 19.07.2021
16. Meet a Guru: Ryan Behringer

    Opublikowany: 14.07.2021
17. Navigating the MedTech Cybersecurity Ecosystem

    Opublikowany: 13.07.2021
18. Managing Clinical Data Activities

    Opublikowany: 7.07.2021
19. Explaining the Role of Importer under EU MDR

    Opublikowany: 1.07.2021
20. Preparing Your Pre-Submission with the Content FDA Wants to See

    Opublikowany: 23.06.2021