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

This article was originally published in Clinica

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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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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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