Page:United States Statutes at Large Volume 106 Part 5.djvu/862

 106 STAT. 4500 PUBLIC LAW 102-571—OCT. 29, 1992 (C) by indenting, and aligning the margins of, subparagraphs (A) and (B) of paragraph (2) (as so designated by subparagraph (A)) so as to align with the subparagraphs of paragraph (1). (17) Section 10(c)(2)(A) of the Nutrition Labeling and Education Act of 1990 (21 U.S.C. 343 note) (as amended by section 1 of the Act entitled "An Act to make Technical Amendments to the Nutrition Information and Labeling Act, and for other purposes**, approved August 17, 1991 (Public Law 102-108; 105 Stat. 549) is amended by striking "706** and inserting " 721**. 21 USC 379g SEC. 108. ANIMAL DRUG USER FEE STUDY. (a) STUDY. — The Secretary, in consultation with manufacturers of animal drug products and other interested persons, shall undertake a study to evaluate whether, and under what conditions, to impose user fees to supplement appropriated funds in order to improve the process of reviewing applications (including abbreviated and supplemental applications) for new animal drugs under section 512 of the Federal Food, Drug, and Cosmetic Act. The study shall include— (1) an assessment of the overall review process for animal drugs at the Center for Veterinary Medicine, including the number of applications received, and the average times for interim and final decisions on each type of application, (2) the current allocation of funds to the animal drug review process, (3) recommendations for goals for decision making times on applications submitted to the Center for Veterinary Medicine and for additional resources required to meet the goals, and (4) recommendations for supplementing the resources for the animal drug review process through user fees. (b) COMPLETION.—The results of the study required by subsection (a) shall be presented no later than January 4, 1994, to the Committee on Energy and Commerce of the House of Representatives and the Committee on Labor and Human Resources of the Senate. sSppi7ment TITLE II—DIETARY SUPPLEMENTS Act of 1992. 21 USC 301 SEC. 201. SHORT TITLE. This title may be cited as the "Dietary Supplement Act of 1992**. SEC. 202. PROHIBITION. 21 USC 343 (a) IN GENERAL. — ^°^- (1) PROHIBITION ON IMPLEMENTATION.—Notwithstanding any other provision of law and except as provided in subsection (b) and in the amendment made by paragraph (2)(A), the Secretary of Health and Human Services may not implement the Nutrition Labeling and Education Act of 1990 (Public Law 101-535; 104 Stat. 2353), or any amendment made by such Act, earlier than December 15, 1993, with respect to dietary supplements of vitamins, minerals, herbs, or other similar nutritional substances. (2) FEDERAL REGULATORY ACTION.—

�