155 Episodo

  1. The Special 510k Program

    Publicado: 13/11/2019
  2. Beyond 510(k)/PMA—Safer Technologies Program

    Publicado: 16/10/2019
  3. Benefit-Risk Determinations

    Publicado: 16/9/2019
  4. Mike on Medtech: Beyond 510(k)/PMA—Breakthrough Devices Program

    Publicado: 6/8/2019
  5. Beyond 510(k)/PMA—De Novo 101

    Publicado: 2/7/2019
  6. Mike on Medtech: The NYT Editorial Board Statement

    Publicado: 17/6/2019
  7. The Alternative Summary Reporting Program

    Publicado: 24/5/2019
  8. Do we need a pre-sub for 483s? (Part 2)

    Publicado: 9/5/2019
  9. Do we need a pre-sub for 483s?

    Publicado: 9/5/2019
  10. FDA's Material Evaluation

    Publicado: 2/4/2019
  11. 510k Modernization

    Publicado: 25/1/2019
  12. Personalized Healthcare

    Publicado: 3/1/2019
  13. My Holiday Wish List (Part 2)

    Publicado: 11/12/2018
  14. My Holiday Wish List (Part 1)

    Publicado: 4/12/2018
  15. Regulating the Practice of Medicine

    Publicado: 26/10/2018
  16. The Bleeding Edge, Part 3

    Publicado: 26/9/2018
  17. The Bleeding Edge, Part 2

    Publicado: 7/9/2018
  18. The Bleeding Edge, Part 1

    Publicado: 5/9/2018
  19. Breakthrough Designation Program

    Publicado: 10/8/2018
  20. 15 Tips for Getting New Products Through FDA

    Publicado: 3/7/2018

7 / 8

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

Visit the podcast's native language site