Home > Research > Publications & Outputs > Marketing authorization of medical devices in C...

Associated organisational unit

Electronic data

  • JCB_2016_Zang_Liu_Chatwin

    Accepted author manuscript, 488 KB, PDF document

    Available under license: CC BY-NC: Creative Commons Attribution-NonCommercial 4.0 International License

Links

Text available via DOI:

View graph of relations

Marketing authorization of medical devices in China

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published
Close
<mark>Journal publication date</mark>2016
<mark>Journal</mark>Journal of Commercial Biotechnology
Issue number1
Volume22
Number of pages8
Pages (from-to)15-22
Publication StatusPublished
Early online date11/05/16
<mark>Original language</mark>English

Abstract

Medical device regulations across the globe have significant variations. The Chinese medical device market, like China's economy, is developing rapidly. This article reviews the medical device regulations in China and illustrates the major changes that have been recently implemented according to the new medical device regulations that came into force on the 1st June, 2014. Most regulatory research has focused on the US and EU medical device regulations with little written about the Chinese medical device regulations. The purpose of this article is to bridge the research gap and to introduce the Chinese medical devices regulatory environment to investors or companies who are engaged in the medical device market or doing business in China