416 Episodo

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

    Publicado: 10/8/2022

  2. Digitizing your SaMD Testing

    Publicado: 3/8/2022

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

    Publicado: 27/7/2022

  4. Guerilla Tactics for Quality Leadership

    Publicado: 20/7/2022

  5. Preventing the Death of Medical Device Sales

    Publicado: 13/7/2022

  6. Shifting Sands of SaMD Cybersecurity Regulations

    Publicado: 6/7/2022

  7. Early Stage Territory Planning for Medical Device Companies

    Publicado: 29/6/2022

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

    Publicado: 22/6/2022

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

    Publicado: 16/6/2022

  10. Early Feasibility Studies in Latin America

    Publicado: 8/6/2022

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

    Publicado: 1/6/2022

  12. Approaching Cybersecurity & Usability as a SaMD Company

    Publicado: 28/5/2022

  13. The Future of Lateral Flow Test Technology

    Publicado: 25/5/2022

  14. Building a Culture of Quality

    Publicado: 20/5/2022

  15. Bringing Medical Devices into the Home

    Publicado: 18/5/2022

  16. Demystifying the De Novo Process

    Publicado: 12/5/2022

  17. Challenges for Regulatory Submission: EU vs. US

    Publicado: 6/5/2022

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

    Publicado: 4/5/2022

  19. The Future of Cybersecurity

    Publicado: 30/4/2022

  20. Achieving Operational Readiness through Good Project Management

    Publicado: 27/4/2022

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The Global Medical Device Podcast, powered by Greenlight Guru, is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.

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