The U.S. Food and Drug Administration has issued a draft guidance to help animal drug sponsors determine an acute reference dose (ARfD), which is the estimate of the amount of residues expressed on a body weight basis that can be ingested in a period of no more than 24 hours or less without adverse effects or harm to the health of the human consumer.
via What's New: Animal & Veterinary http://ift.tt/1PSl73z
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