416 Odcinki

  1. #334: MedTech Funding and Preparing for Due Diligence

    Opublikowany: 31.08.2023

  2. #333: Exploring Breakthrough Device Designation

    Opublikowany: 25.08.2023

  3. #332: Regulatory Strategy and the Advantage of Diversity in MedTech

    Opublikowany: 17.08.2023

  4. #331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues

    Opublikowany: 10.08.2023

  5. #330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?

    Opublikowany: 3.08.2023

  6. #329 The Right Way to Start a QMS: When, How, & What

    Opublikowany: 27.07.2023

  7. #328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices

    Opublikowany: 20.07.2023

  8. #327 Understanding the ROI of an eQMS

    Opublikowany: 11.07.2023

  9. #326 CSA vs. CSV: Modern Validation for Modern MedTech

    Opublikowany: 7.07.2023

  10. #325 The Role of dFMEAs in Risk Management for Medical Devices

    Opublikowany: 30.06.2023

  11. #325 The Role of dFMEAs in Risk Management for Medical Devices

    Opublikowany: 29.06.2023

  12. #324 Management Responsibility: The most important part of a QMS

    Opublikowany: 22.06.2023

  13. #323 The Combination Products Handbook

    Opublikowany: 16.06.2023

  14. Leaning into Lean Documentation

    Opublikowany: 7.06.2023

  15. Cybersecurity and the Future of MedTech

    Opublikowany: 2.06.2023

  16. How AI Can Help You Manage Risk

    Opublikowany: 26.05.2023

  17. Ad Promo and The Difference in Regulatory & Legal

    Opublikowany: 24.05.2023

  18. The Tools that Make Clinical Investigations

    Opublikowany: 13.05.2023

  19. Complaint Handling with Medical Device Guru, Brittney McIver

    Opublikowany: 3.05.2023

  20. Avoiding Potential Issues with your 510(k) Submission

    Opublikowany: 27.04.2023

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