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Entreprise · 23/12/20021 min de lecture
Revision of the Definition of the Term “No Residue” in the New Animal Drug Regulations
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Résumé
The Food and Drug Administration (FDA) is amending its regulations regarding carcinogenic compounds used in food-producing animals. Specifically, FDA is deleting the operational definition of the term "no residue" and is making conforming amendments to other parts of these regulations. FDA is making these amendments in response to a legal opinion issued by the Department of Justice (DOJ), Office of Legal Counsel, which concluded that the operational definition of "no residue" is not legally supportable.
Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →