Selling your medical device in the global marketplace requires you to consider other languages and cultures. There are over 20 official languages in Europe alone and thousands more worldwide. How is it possible to provide necessary information about your medical device to a diverse group of users?
The use of symbols and the adoption of electronic labeling (e-labeling), where possible, help simplify product labeling while also providing sufficient information for users. In this white paper, we'll answer your biggest questions about standards, requirements, and symbols for medical device labeling, including:
You will learn all this and more in this 9-page white paper.
为了获得澳大利亚市场准入,医疗器械和体外诊断(IVD)器械制造商需要将他们的产品列入由药品管理局(TGA)监管的澳大利亚医疗用品登记表(ARTG)。
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