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.
Since the publication of ISO 13485:2016, risk management is a major concern for maintaining regulatory compliance in major medical device markets.
read morePost-market Clinical Follow-up (PMCF) is an important part of ongoing medical device regulatory compliance in the EU. PMCF can sometimes require yo
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