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Published in 2019 at "Trends in biotechnology"
DOI: 10.1016/j.tibtech.2018.06.005
Abstract: Medicinal products based on genome editing must undergo rigorous preclinical testing and are subject to regulatory oversight for proper risk assessment prior to first evaluation in humans. We give a European perspective on the regulatory…
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Keywords:
genome editing;
race loosening;
human genome;
editing race ... See more keywords