EMEA pharmaceutical news in brief

Published: 25-Mar-2008


The European Medicines Agency (EMEA) has released detailed advice on Assessing the toxicity of medicines in animal tests; and it has issued guidance on the need for
Non-clinical testing in juvenile animals to assess human medicines effect on children .

EMEA has published guidelines recommending maximum acceptable concentration limits for the residues of metal catalysts or metal reagents in pharmaceuticals; it has also released guidance on Sampling and testing authorised medicines; and on its Procedures for co-ordinating pharmacovigilance inspections;

And the agency has published a paper on revising its Guidance on photosafety testing .

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Sapio Sciences introduces world’s first 3rd-generation ELN

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Genoskin raises $8.7m in its first funding round to advance its ethical, human-based alternatives to animal testing

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