What is Difference between in the ISO 13485 and FDA 21 CFR Part 820 for Medical Device

Discussion in 'Medical Equipment/Device Sales-General Discussion' started by Neha, Sep 19, 2018 at 7:11 AM.

  1. Neha

    Neha new user

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    Want to know about the registration process for medical device and also what is the difference between ISO 13485 and FDA 21 CFR Part 820?
     

  2. anonymous

    anonymous Guest

    Is your google machine broken?