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Commission unveils details on plan for phasing out animaltesting for chemicals safety At the REACH and CLP regulators’ meeting in July, the European Commission revealed specifics about its formal schedule to eliminate animaltesting used for chemical safety assessment.
Commission redoubles commitment to reduce animaltesting in response to Citizens’ Initiative The European Commission provided its mandatory response to a citizens’ petition this week urging faster action to reduce and ultimately eliminate animaltesting within the cosmetics and chemical sectors.
This shift occurred following implementation of the Comprehensive in Vitro Proarrhythmia Assay (CiPA) initiative in 2013 and extensive testing of hiPSC-cardiomyocytes with known proarrhythmic drugs.
Notifications will need to include the specific data requirements as laid out in Regulation (EU) No 283/2013 in Sections 1.3, of Part A of the Annex and “evidence that the notified substance or preparation is used as a safener or synergist in at least one plant protection product authorised in at least one Member State.”
As a result, the FDA is now required to consider alternatives to animaltesting, such as in vitro , in silico , and in chemico tests and models. In this blog post, we examine several alternative approaches to animaltesting and how the FDA handles the application of these methods in specific scenarios.
Though my focus in this essay is narrow — I don’t discuss bottlenecks in clinical trials, human disease, or animaltesting — I hope others will take on these challenges in similar essays. This essay focuses on how we might do both, specifically for the cell. Subscribe to Asimov Press. Credit: SIngh U.S.
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