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Zdrowie i gospodarka · 3.05.2005

Agency Information Collection Activities; Proposed Collection; Comment Request; Extralabel Drug Use in Animals

The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the Paperwork Reduction Act of 1995, (the PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension for an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the reporting requirements when development of an analytical method for residue detection is required by FDA for a drug prescribed for extralabel use in animals.

Source: Federal Register — Food and Drug AdministrationOpen original release →
Related company profile: AlabOpen profile →