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Medical Device

Not yet "case closed" on EU's human tissue product regulation?

This article was originally published in Clinica

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Executive Summary

There is still sufficient strong feeling among those representing medical device manufacturers over the regulation of human tissue engineered products (hTEPS) to suggest that the debate within the European Council on the European Commission's proposed Regulation for Advanced Therapy Products could be both lively and complex.

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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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