Global Medical Device Podcast powered by Greenlight Guru

416 Episoade

1. The Changing Job Market & How It Affects Careers for MedTech Quality Professionals

   Publicat: 10.08.2022
2. Digitizing your SaMD Testing

   Publicat: 03.08.2022
3. Examining FDA’s Refusal to Accept (RTA) Policy and Guidance

   Publicat: 27.07.2022
4. Guerilla Tactics for Quality Leadership

   Publicat: 20.07.2022
5. Preventing the Death of Medical Device Sales

   Publicat: 13.07.2022
6. Shifting Sands of SaMD Cybersecurity Regulations

   Publicat: 06.07.2022
7. Early Stage Territory Planning for Medical Device Companies

   Publicat: 29.06.2022
8. Regulatory & Quality Perspectives of 3D Printing in the Medical Device Industry

   Publicat: 22.06.2022
9. What Impact Does a QMS & Regulatory Have on Fundraising and Pre-money Valuation?

   Publicat: 16.06.2022
10. Early Feasibility Studies in Latin America

    Publicat: 08.06.2022
11. Software Bill of Materials (SBOMs) & Cybersecurity in the Medical Device Industry

    Publicat: 01.06.2022
12. Approaching Cybersecurity & Usability as a SaMD Company

    Publicat: 28.05.2022
13. The Future of Lateral Flow Test Technology

    Publicat: 25.05.2022
14. Building a Culture of Quality

    Publicat: 20.05.2022
15. Bringing Medical Devices into the Home

    Publicat: 18.05.2022
16. Demystifying the De Novo Process

    Publicat: 12.05.2022
17. Challenges for Regulatory Submission: EU vs. US

    Publicat: 06.05.2022
18. From Startup to Industry Leader: LIVE RECORDING AT SCBIO CONFERENCE

    Publicat: 04.05.2022
19. The Future of Cybersecurity

    Publicat: 30.04.2022
20. Achieving Operational Readiness through Good Project Management

    Publicat: 27.04.2022