Report Includes:

  • Detailed description of the regulatory requirements for marketing and registration of medical devices in the U.S.
  • Insights into the current regulations and comprehensive procedures for the registration, renewal or notification of the medical devices, along with the information on timeline and fee required
  • Knowledge about labelling and advertising regulations for the medical device and details of the process for registration of the product with any specific variation
  • Information on Federal Food, Drug, and Cosmetic Act (the Act) and how it works towards the betterment of society