FDA Regulations and Medical Device Pathways to Market

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  • Опубліковано 27 лис 2024

КОМЕНТАРІ • 11

  • @meenakshirana6467
    @meenakshirana6467 8 років тому +1

    It's a very informative presentation. Thank you very much for uploading it.

  • @Elizabethterhune
    @Elizabethterhune 7 років тому

    Great presentation, thank you! I used it to help study for my bioregulations exam. Super helpful.

  • @MysterERaps
    @MysterERaps 5 років тому +1

    I'm curious how 300k to a million for initial costs on a class 1 device breaks down, budget wise

  • @saurabh5534
    @saurabh5534 6 років тому

    In 510k, the product gets cleared by USFDA but you mentioned as approved? please clarify sir

  • @j.6946
    @j.6946 5 років тому

    Great presentation, thanks so much. This is very helpful.

  • @dennychoi4439
    @dennychoi4439 5 років тому

    Great video ! thanks a lot

  • @leeswanson2766
    @leeswanson2766 7 років тому +1

    CFR = Code of Federal Regulations

    • @sptzk7133
      @sptzk7133 4 роки тому

      CFR does stand for code of federal regulations however the federal register or congressional federal registry he referred to seems to be the daily discussions of these laws and once they are finalized they are introduced into the CFR. So it seems it is reasonable to misspeak, I only look this up because I wasn’t sure if the lecture was credible, but looks like it is:)

  • @dianawright6975
    @dianawright6975 4 роки тому

    Can anyone have one