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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.
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