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ENVI strengthens case for non-viables as it tackles ethically-controversial issues

This article was originally published in Clinica

Executive Summary

The latest draft report put together by Miroslav Mikolasik, rapporteur at the European Parliament's Committee on the Environment Public Health and Food Safety (ENVI), on the European Commission's proposed Advanced Therapies Medicinal Products (ATMP) Regulation, is currently devoid of any of the ethically-controversial issues that caused it to founder when MEPs last voted on the text.

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