118 STAT. 905 PUBLIC LAW 108–282—AUG. 2, 2004 (T) Section 108(b)(3) of Public Law 90–399 is amended by striking ‘‘section 201(w) as added by this Act’’ and inserting ‘‘section 201(v)’’. (6) REGULATIONS.—On the date of enactment of this Act, the Secretary of Health and Human Services shall implement sections 571 and 573 of the Federal Food, Drug, and Cosmetic Act and subsequently publish implementing regulations. Not later than 12 months after the date of enactment of this Act, the Secretary shall issue proposed regulations to implement section 573 of the Federal Food, Drug, and Cosmetic Act (as added by this Act), and not later than 24 months after the date of enactment of this Act, the Secretary shall issue final regulations implementing section 573 of the Federal Food, Drug, and Cosmetic Act. Not later than 18 months after the date of enactment of this Act, the Secretary shall issue proposed regulations to implement section 572 of the Federal Food, Drug, and Cosmetic Act (as added by this Act), and not later than 36 months after the date of enactment of this Act, the Secretary shall issue final regulations implementing section 572 of the Federal Food, Drug, and Cosmetic Act. Not later than 30 months after the date of enactment of this Act, the Secretary shall issue proposed regulations to implement section 571 of the Federal Food, Drug, and Cosmetic Act (as added by this Act), and not later than 42 months after the date of enactment of this Act, the Secretary shall issue final regulations imple menting section 571 of the Federal Food, Drug, and Cosmetic Act. These timeframes shall be extended by 12 months for each fiscal year, in which the funds authorized to be appro priated under subsection (i) are not in fact appropriated. (7) OFFICE.—The Secretary of Health and Human Services shall establish within the Center for Veterinary Medicine (of the Food and Drug Administration), an Office of Minor Use and Minor Species Animal Drug Development that reports directly to the Director of the Center for Veterinary Medicine. This office shall be responsible for overseeing the development and legal marketing of new animal drugs for minor uses and minor species. There is authorized to be appropriated to carry out this subsection $1,200,000 for fiscal year 2004 and such sums as may be necessary for each fiscal year thereafter. (8) AUTHORIZATION OF APPROPRIATIONS.—There is author ized to be appropriated to carry out section 573(b) of the Federal Food, Drug, and Cosmetic Act (as added by this section) $1,000,000 for the fiscal year following publication of final implementing regulations, $2,000,000 for the subsequent fiscal year, and such sums as may be necessary for each fiscal year thereafter. TITLE II—FOOD ALLERGEN LABELING AND CONSUMER PROTECTION SEC. 201. SHORT TITLE. This title may be cited as the ‘‘Food Allergen Labeling and Consumer Protection Act of 2004’’. SEC. 202. FINDINGS. Congress finds that— 21 USC 343 note. 21 USC 301 note. Food Allergen Labeling and Consumer Protection Act of 2004. Appropriation authorization. Government organization. 21 USC 393 note. Effective date. Deadlines. Publication. 21 USC 360ccc note. 21 USC 360b note.
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