Zdrowie i gospodarka · 28/01/2002

FDA Seeks Public Comment on Proposed Collection of Information for Extralabel Drug Use in Animals

The Food and Drug Administration (FDA) is seeking public comment on a proposed collection of information related to residue detection methodology for human or animal drugs prescribed for extralabel use in animals. The agency is required to publish this notice under the Paperwork Reduction Act of 1995 and allow 60 days for public comment.