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2007/47/EC: why buying standards revisions can be frustrating

This article was originally published in Clinica

Executive Summary

Manufacturers and consultants in the UK, and very likely elsewhere in the EU, who need to keep abreast with the latest standards changes may be questioning the costs of standards revised in the light of Directive 2007/47/EC which amends the medical device directives, given how minor some of the changes may be.

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