398 Episoder

  1. Does Your CAPA Process Need a CAPA?

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

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

    Publisert: 10.8.2022
  4. Digitizing your SaMD Testing

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

    Publisert: 27.7.2022
  6. Guerilla Tactics for Quality Leadership

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

    Publisert: 13.7.2022
  8. Shifting Sands of SaMD Cybersecurity Regulations

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

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

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

    Publisert: 16.6.2022
  12. Early Feasibility Studies in Latin America

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

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

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

    Publisert: 25.5.2022
  16. Building a Culture of Quality

    Publisert: 20.5.2022
  17. Bringing Medical Devices into the Home

    Publisert: 19.5.2022
  18. Demystifying the De Novo Process

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

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

    Publisert: 4.5.2022

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