Sec. 901. Technical corrections

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Section 3075(a) of the 21st Century Cures Act ( Public Law 114–255 ) is amended— in the matter preceding paragraph (1), by striking as amended by section 2074 and inserting as amended by section 3102 ; and in paragraph (2), by striking section 2074(1)(C) and inserting section 3102(1)(C) . Section 506G(b)(1)(A) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 356g(b)(1)(A) ) is amended by striking identity and inserting identify . Section 505F(b) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 355g(b) ) is amended by striking randomized and inserting traditional .

Section 505F(d) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 355g(d) ) is amended by striking 2 and inserting 3 . Section 510(h)(6) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 360(h)(6) ) is amended by striking February 1 and replacing with May 1 . Effective as of the enactment of the 21st Century Cures Act ( Public Law 114–255 )— section 3051(a) of such Act is amended by striking by inserting after section 515B and inserting by inserting after section 515A ; and section 515C of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 360e–3 ), as inserted by such section 3051(a), is redesignated as section 515B.

Section 515B(f)(2) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 360e–3(f)(2) ), as redesignated by subsection (e)(2) of this section, is amended by striking a proposed guidance and inserting a draft version of that guidance . Section 513(b)(5)(D) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 360c(b)(5)(D) ) is amended by striking medical device submissions and inserting medical devices that may be specifically the subject of a review by a classification panel .

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