Global Medical Device Podcast powered by Greenlight Guru

416 Episodio

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

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

   Pubblicato: 03/11/2021
3. Project Management for Product Development of Medical Devices

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

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

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

   Pubblicato: 06/10/2021
7. Past, Present, Future State (and World) of Quality in the Medical Device Industry

   Pubblicato: 22/09/2021
8. Focusing on the Intent of the UDI Requirements from FDA's Final Guidance Doc

   Pubblicato: 16/09/2021
9. Addressing the 'Who, What, When' of Quality in the Medical Device Industry

   Pubblicato: 08/09/2021
10. Meet a Guru: Maryann Mitchell

    Pubblicato: 02/09/2021
11. Why Storytelling Matters for Medical Device Companies

    Pubblicato: 25/08/2021
12. A Breakthrough Device that Aims to Prevent Osteoporosis

    Pubblicato: 19/08/2021
13. Understanding FDA's New Intended Use Rule and its Implications

    Pubblicato: 11/08/2021
14. eQMS in Academia: Practical Learning for Biomedical Engineering Students

    Pubblicato: 28/07/2021
15. Tips for Running Better Management Reviews

    Pubblicato: 19/07/2021
16. Meet a Guru: Ryan Behringer

    Pubblicato: 14/07/2021
17. Navigating the MedTech Cybersecurity Ecosystem

    Pubblicato: 13/07/2021
18. Managing Clinical Data Activities

    Pubblicato: 07/07/2021
19. Explaining the Role of Importer under EU MDR

    Pubblicato: 01/07/2021
20. Preparing Your Pre-Submission with the Content FDA Wants to See

    Pubblicato: 23/06/2021