A drug safety test that uses thousands of laboratory mice and rats each year in Europe is no longer necessary, a review involving 18 pharmaceutical companies and contract research organisations has ...
On March 17, 2021, the U.S. Environmental Protection Agency (EPA) announced the issuance of the final guidance document entitled "Guidance for Waiving Acute Dermal Toxicity Tests for Pesticide ...
TruLarv ™ is considered a non-animal technology (NAT) in the context of UK animal use regulations (ASPA) where procedures on this species are not regulated. We carried out a study in partnership with ...
Washington -- A report outlining the findings of the international expert workshop "Alternative Approaches for Identifying Acute Systemic Toxicity: Moving From Research to Regulatory Testing" was ...
Dublin, Sept. 15, 2023 (GLOBE NEWSWIRE) -- The "In Vitro Toxicity Testing Market, By Type, By End User, and By Region- Size, Share, Outlook, and Opportunity Analysis, 2023 - 2030" report has been ...
DOD needs to understand the relative threat of the increasingly long list of registered chemical substances, particularly in terms of potential acute hazard. To help DOD achieve its goal to protect ...
The committee explored whether DOD could adopt a modern testing strategy for the prediction of acute toxicity. 3 In particular, the committee’s statement of task required a focus on the assessment of ...
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