For termination of section by section 4005(b) of Pub. L. 117–180, see Effective and Termination Dates note set out below.
Section 401(b) of the Biosimilar User Fee Amendments of 2022, referred to in subsecs. (a) and (c), probably should be a reference to section 4001(b) of the Biosimilar User Fee Amendments of 2022, title IV of div. F of Pub. L. 117–180, which is set out as a note under section 379j–51 of this title. The Biosimilar User Fee Amendments of 2022 does not contain a section 401(b).
Section 4001(b) of the Biosimilar User Fee Amendments of 2022, referred to in subsec. (a)(4)(A), is section 4001(b) of title IV of div. F of Pub. L. 117–180, which is set out as a note under section 379j–51 of this title.
Amendments made by section 904(d)(2) of Pub. L. 115–52, effective
2022—Pub. L. 117–180, § 4004(2), substituted “Biosimilar User Fee Amendments of 2022” for “Biosimilar User Fee Amendments of 2017” wherever appearing.
Subsec. (a)(1). Pub. L. 117–180, § 4004(1), substituted “Not” for “Beginning with fiscal year 2018, not”.
Subsec. (a)(2). Pub. L. 117–180, § 4004(3), substituted “The” for “Beginning with fiscal year 2018, the” in introductory provisions.
Subsec. (a)(3)(A). Pub. L. 117–180, § 4004(4), substituted “Not later than 30 calendar days after the end of each quarter of each fiscal year for which fees are collected under this subpart” for “Not later than 30 calendar days after the end of the second quarter of fiscal year 2018, and not later than 30 calendar days after the end of each quarter of each fiscal year thereafter”.
Subsec. (a)(4)(A). Pub. L. 117–328, § 3626(d)(1)(A), amended subpar. (A) generally. Prior to amendment, subpar. (A) read as follows: “data, analysis, and discussion of the changes in the number of full-time equivalents hired as agreed upon in the letters described in section 401(b) of the Biosimilar User Fee Amendments of 2022 and the number of full time equivalents funded by budget authority at the Food and Drug Administration by each division within the Center for Drug Evaluation and Research, the Center for Biologics Evaluation and Research, the Office of Regulatory Affairs, and the Office of the Commissioner;”.
Subsec. (a)(4)(B). Pub. L. 117–328, § 3626(d)(1)(B), amended subpar. (B) generally. Prior to amendment, subpar. (B) read as follows: “data, analysis, and discussion of the changes in the fee revenue amounts and costs for the process for the review of biosimilar biological product applications, including identifying drivers of such changes; and”.
Subsec. (a)(4)(D). Pub. L. 117–328, § 3626(d)(1)(C), (D), added subpar. (D).
Subsec. (b). Pub. L. 117–180, § 4004(5), substituted “Not later than 120 days after the end of each fiscal year for which fees are collected under this subpart” for “Not later than 120 days after the end of fiscal year 2018 and each subsequent fiscal year for which fees are collected under this subpart”.
Subsec. (c). Pub. L. 117–180, § 4004(6), substituted “For” for “Beginning with fiscal year 2018, and for” in introductory provisions.
Subsec. (f)(1). Pub. L. 117–180, § 4004(7)(A), substituted “fiscal year 2027” for “fiscal year 2022” in introductory provisions.
Subsec. (f)(2). Pub. L. 117–328, § 3626(d)(2)(B), added par. (2). Former par. (2) redesignated (5).
Subsec. (f)(3). Pub. L. 117–328, § 3626(d)(2)(B), added par. (3). Former par. (3) redesignated (6).
Pub. L. 117–180, § 4004(7)(B), substituted “
Subsec. (f)(4) to (7). Pub. L. 117–328, § 3626(d)(2), added pars. (4) and (7) and redesignated formers pars. (2) and (3) as (5) and (6), respectively.
2017—Subsec. (a). Pub. L. 115–52, § 903(d), designated existing provisions as par. (1), inserted heading, and added pars. (2) to (4).
Pub. L. 115–52, § 404(1), substituted “2018” for “2013” and “Biosimilar User Fee Amendments of 2017” for “Biosimilar User Fee Act of 2012”.
Subsec. (a)(5). Pub. L. 115–52, § 904(d)(1), added par. (5).
Subsec. (b). Pub. L. 115–52, § 404(2), substituted “2018” for “2013”.
Subsec. (c). Pub. L. 115–52, § 904(d)(2), added subsec. (c). Former subsec. (c) redesignated (e).
Subsecs. (d), (e). Pub. L. 115–52, § 904(d)(2), added subsec. (d) and redesignated subsec. (c) as (e). Former subsec. (d), as redesignated by section 404(4) of Pub. L. 115–52, redesignated (f). See Amendment notes below.
Pub. L. 115–52, § 404(3)–(5), redesignated subsec. (e) as (d), substituted “2022” for “2017” in pars. (1) and (3), and struck out former subsec. (d) which related to a study of the workload volume and full costs associated with the process for the review of biosimilar biological product applications.
Subsec. (f). Pub. L. 115–52, § 904(d)(2), redesignated subsec. (d) as (f).
Amendment by Pub. L. 117–180 effective
Amendment by section 404 of Pub. L. 115–52 effective
Pub. L. 117–180, div. F, title IV, § 4005(b),
Pub. L. 115–52, title IV, § 405(b),
[Pub. L. 117–180, div. F, title IV, § 4005(c),
Pub. L. 112–144, title IV, § 404(b),
[Pub. L. 115–52, title III, § 405(c)(1),
Section effective