Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. Does Your CAPA Process Need a CAPA?

   Udgivet: 24.8.2022
2. UDI and the Current State of Global Implementation

   Udgivet: 18.8.2022
3. The Changing Job Market & How It Affects Careers for MedTech Quality Professionals

   Udgivet: 10.8.2022
4. Digitizing your SaMD Testing

   Udgivet: 3.8.2022
5. Examining FDA’s Refusal to Accept (RTA) Policy and Guidance

   Udgivet: 27.7.2022
6. Guerilla Tactics for Quality Leadership

   Udgivet: 20.7.2022
7. Preventing the Death of Medical Device Sales

   Udgivet: 13.7.2022
8. Shifting Sands of SaMD Cybersecurity Regulations

   Udgivet: 6.7.2022
9. Early Stage Territory Planning for Medical Device Companies

   Udgivet: 29.6.2022
10. Regulatory & Quality Perspectives of 3D Printing in the Medical Device Industry

    Udgivet: 23.6.2022
11. What Impact Does a QMS & Regulatory Have on Fundraising and Pre-money Valuation?

    Udgivet: 16.6.2022
12. Early Feasibility Studies in Latin America

    Udgivet: 8.6.2022
13. Software Bill of Materials (SBOMs) & Cybersecurity in the Medical Device Industry

    Udgivet: 2.6.2022
14. Approaching Cybersecurity & Usability as a SaMD Company

    Udgivet: 28.5.2022
15. The Future of Lateral Flow Test Technology

    Udgivet: 25.5.2022
16. Building a Culture of Quality

    Udgivet: 20.5.2022
17. Bringing Medical Devices into the Home

    Udgivet: 19.5.2022
18. Demystifying the De Novo Process

    Udgivet: 12.5.2022
19. Challenges for Regulatory Submission: EU vs. US

    Udgivet: 6.5.2022
20. From Startup to Industry Leader: LIVE RECORDING AT SCBIO CONFERENCE

    Udgivet: 4.5.2022