416 Epizód

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

    Közzétéve: 2023. 08. 31.

  2. #333: Exploring Breakthrough Device Designation

    Közzétéve: 2023. 08. 25.

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

    Közzétéve: 2023. 08. 17.

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

    Közzétéve: 2023. 08. 10.

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

    Közzétéve: 2023. 08. 03.

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

    Közzétéve: 2023. 07. 27.

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

    Közzétéve: 2023. 07. 20.

  8. #327 Understanding the ROI of an eQMS

    Közzétéve: 2023. 07. 11.

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

    Közzétéve: 2023. 07. 07.

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

    Közzétéve: 2023. 06. 30.

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

    Közzétéve: 2023. 06. 29.

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

    Közzétéve: 2023. 06. 22.

  13. #323 The Combination Products Handbook

    Közzétéve: 2023. 06. 16.

  14. Leaning into Lean Documentation

    Közzétéve: 2023. 06. 07.

  15. Cybersecurity and the Future of MedTech

    Közzétéve: 2023. 06. 02.

  16. How AI Can Help You Manage Risk

    Közzétéve: 2023. 05. 26.

  17. Ad Promo and The Difference in Regulatory & Legal

    Közzétéve: 2023. 05. 24.

  18. The Tools that Make Clinical Investigations

    Közzétéve: 2023. 05. 13.

  19. Complaint Handling with Medical Device Guru, Brittney McIver

    Közzétéve: 2023. 05. 03.

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

    Közzétéve: 2023. 04. 27.

5 / 21

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