|
Home
>
Newsletters
>
International Medical Device Regulatory Monitor
> Navigating China’s Labeling, Ad Regulations: An Expert’s Guide
International Medical Device Regulatory Monitor
April 2012
| Vol.
20 No.
4
Navigating China’s Labeling, Ad Regulations: An Expert’s Guide
Simply translating a medical device’s instructions for use (IFU) from the original language into Chinese will likely land foreign devicemakers in the regulatory hot seat, according to Vic Zhang, director of regulatory affairs-China for Smith & Nephew’s Advanced Surgical Devices Division.
|
|
ePublishing :: CMS, Hosting & Web Development | © Copyright by FDAnews
All rights reserved. Do not duplicate or redistribute in any form.