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Euro devices industry ponders issue of self-regulation: is there more change to come?

This article was originally published in Clinica

Executive Summary

How will the regulation of medical devices change over the next ten years? Is there enough flexibility in the system to allow for a greater degree of self-regulation? Are notified bodies really needed? These were among the issues at a medical device industry networking organised by the IQA in London on April 6. Amanda Maxwell reports

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