Global Medical Device Podcast powered by Greenlight Guru

398 Episodes

1. Does Your CAPA Process Need a CAPA?

   Published: 8/24/2022
2. UDI and the Current State of Global Implementation

   Published: 8/18/2022
3. The Changing Job Market & How It Affects Careers for MedTech Quality Professionals

   Published: 8/10/2022
4. Digitizing your SaMD Testing

   Published: 8/3/2022
5. Examining FDA’s Refusal to Accept (RTA) Policy and Guidance

   Published: 7/27/2022
6. Guerilla Tactics for Quality Leadership

   Published: 7/20/2022
7. Preventing the Death of Medical Device Sales

   Published: 7/13/2022
8. Shifting Sands of SaMD Cybersecurity Regulations

   Published: 7/6/2022
9. Early Stage Territory Planning for Medical Device Companies

   Published: 6/29/2022
10. Regulatory & Quality Perspectives of 3D Printing in the Medical Device Industry

    Published: 6/23/2022
11. What Impact Does a QMS & Regulatory Have on Fundraising and Pre-money Valuation?

    Published: 6/16/2022
12. Early Feasibility Studies in Latin America

    Published: 6/8/2022
13. Software Bill of Materials (SBOMs) & Cybersecurity in the Medical Device Industry

    Published: 6/2/2022
14. Approaching Cybersecurity & Usability as a SaMD Company

    Published: 5/28/2022
15. The Future of Lateral Flow Test Technology

    Published: 5/25/2022
16. Building a Culture of Quality

    Published: 5/20/2022
17. Bringing Medical Devices into the Home

    Published: 5/19/2022
18. Demystifying the De Novo Process

    Published: 5/12/2022
19. Challenges for Regulatory Submission: EU vs. US

    Published: 5/6/2022
20. From Startup to Industry Leader: LIVE RECORDING AT SCBIO CONFERENCE

    Published: 5/4/2022