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Medical Device

Japan urges build-up of data

This article was originally published in Clinica

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Executive Summary

Japan's new medical devices master file system, a raw material registration database, needs more support from companies to make it work. The system allows product applicants to refer to already registered data as a means of abbreviating their product applications, and thereby shorten the time it takes to get products onto the market.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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