416 Avsnitt

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

    Publicerades: 2023-08-31

  2. #333: Exploring Breakthrough Device Designation

    Publicerades: 2023-08-25

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

    Publicerades: 2023-08-17

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

    Publicerades: 2023-08-10

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

    Publicerades: 2023-08-03

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

    Publicerades: 2023-07-27

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

    Publicerades: 2023-07-20

  8. #327 Understanding the ROI of an eQMS

    Publicerades: 2023-07-11

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

    Publicerades: 2023-07-07

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

    Publicerades: 2023-06-30

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

    Publicerades: 2023-06-29

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

    Publicerades: 2023-06-22

  13. #323 The Combination Products Handbook

    Publicerades: 2023-06-16

  14. Leaning into Lean Documentation

    Publicerades: 2023-06-07

  15. Cybersecurity and the Future of MedTech

    Publicerades: 2023-06-02

  16. How AI Can Help You Manage Risk

    Publicerades: 2023-05-26

  17. Ad Promo and The Difference in Regulatory & Legal

    Publicerades: 2023-05-24

  18. The Tools that Make Clinical Investigations

    Publicerades: 2023-05-13

  19. Complaint Handling with Medical Device Guru, Brittney McIver

    Publicerades: 2023-05-03

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

    Publicerades: 2023-04-27

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