155 Avsnitt

  1. The Special 510k Program

    Publicerades: 2019-11-13

  2. Beyond 510(k)/PMA—Safer Technologies Program

    Publicerades: 2019-10-16

  3. Benefit-Risk Determinations

    Publicerades: 2019-09-16

  4. Mike on Medtech: Beyond 510(k)/PMA—Breakthrough Devices Program

    Publicerades: 2019-08-06

  5. Beyond 510(k)/PMA—De Novo 101

    Publicerades: 2019-07-02

  6. Mike on Medtech: The NYT Editorial Board Statement

    Publicerades: 2019-06-17

  7. The Alternative Summary Reporting Program

    Publicerades: 2019-05-24

  8. Do we need a pre-sub for 483s? (Part 2)

    Publicerades: 2019-05-09

  9. Do we need a pre-sub for 483s?

    Publicerades: 2019-05-09

  10. FDA's Material Evaluation

    Publicerades: 2019-04-02

  11. 510k Modernization

    Publicerades: 2019-01-25

  12. Personalized Healthcare

    Publicerades: 2019-01-03

  13. My Holiday Wish List (Part 2)

    Publicerades: 2018-12-11

  14. My Holiday Wish List (Part 1)

    Publicerades: 2018-12-04

  15. Regulating the Practice of Medicine

    Publicerades: 2018-10-26

  16. The Bleeding Edge, Part 3

    Publicerades: 2018-09-26

  17. The Bleeding Edge, Part 2

    Publicerades: 2018-09-07

  18. The Bleeding Edge, Part 1

    Publicerades: 2018-09-05

  19. Breakthrough Designation Program

    Publicerades: 2018-08-10

  20. 15 Tips for Getting New Products Through FDA

    Publicerades: 2018-07-03

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A podcast focused on the medical device technology industry, from design and development to outsourcing services and relationships to finished medtech products.

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