Global Medical Device Podcast powered by Greenlight Guru

416 Afleveringen

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

   Gepubliceerd: 10-8-2022
2. Digitizing your SaMD Testing

   Gepubliceerd: 3-8-2022
3. Examining FDA’s Refusal to Accept (RTA) Policy and Guidance

   Gepubliceerd: 27-7-2022
4. Guerilla Tactics for Quality Leadership

   Gepubliceerd: 20-7-2022
5. Preventing the Death of Medical Device Sales

   Gepubliceerd: 13-7-2022
6. Shifting Sands of SaMD Cybersecurity Regulations

   Gepubliceerd: 6-7-2022
7. Early Stage Territory Planning for Medical Device Companies

   Gepubliceerd: 29-6-2022
8. Regulatory & Quality Perspectives of 3D Printing in the Medical Device Industry

   Gepubliceerd: 22-6-2022
9. What Impact Does a QMS & Regulatory Have on Fundraising and Pre-money Valuation?

   Gepubliceerd: 16-6-2022
10. Early Feasibility Studies in Latin America

    Gepubliceerd: 8-6-2022
11. Software Bill of Materials (SBOMs) & Cybersecurity in the Medical Device Industry

    Gepubliceerd: 1-6-2022
12. Approaching Cybersecurity & Usability as a SaMD Company

    Gepubliceerd: 28-5-2022
13. The Future of Lateral Flow Test Technology

    Gepubliceerd: 25-5-2022
14. Building a Culture of Quality

    Gepubliceerd: 20-5-2022
15. Bringing Medical Devices into the Home

    Gepubliceerd: 18-5-2022
16. Demystifying the De Novo Process

    Gepubliceerd: 12-5-2022
17. Challenges for Regulatory Submission: EU vs. US

    Gepubliceerd: 6-5-2022
18. From Startup to Industry Leader: LIVE RECORDING AT SCBIO CONFERENCE

    Gepubliceerd: 4-5-2022
19. The Future of Cybersecurity

    Gepubliceerd: 30-4-2022
20. Achieving Operational Readiness through Good Project Management

    Gepubliceerd: 27-4-2022