Regulatory Intelligence Report for Medical Devices in the U.S.

Mar 2020| MDS006A| BCC Publishing

Report Highlights

The goals of this study were to understand the regulations and requirements of the companies in the US and the foreign companies or establishments planning to manufacture, distribute or market their medical devices in the US. This report provides a brief about the related regulation for registration of the establishments or medical devices along with the classification of the devices.

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


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Analyst Credentials

BCC Publishing Staff comprises expert analysts who are skilled in conducting primary research, secondary research and data analysis and have decades of combined experience covering a wide range of industries, including healthcare, advanced materials and emerging technologies. Collectively, the team represents a diverse set of educational achievements with individual graduate work completed in fields such as microbiology, electrical engineering, business administration and surgery, among others.

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Table of Contents & Pricing

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Title/Chapter NamePagesPrice Member Price
Full Report: Regulatory Intelligence Report for Medical Devices in the U.S.11 $2,500 Free
Regulatory Intelligence Report for Medical Devices in the U.S.

Single User License: $2500

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