§360bbb–8a. Optimizing global clinical trials
Enacted 2012 · amended 1 time, last in 2016 · reading the current textFull lineage →
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Latest NOW As last amended Dec 13, 2016 — Pub. L. 114–255 As originally enacted Jul 9, 201221 U.S.C. § 360bbb–8a
work with other regulatory authorities of similar standing, medical research companies, and international organizations to foster and encourage uniform, scientifically driven clinical trial standards with respect to medical products around the world; and
enhance the commitment to provide consistent parallel scientific advice to manufacturers seeking simultaneous global development of new medical products in order to—
enhance medical product development;
facilitate the use of foreign data; and
minimize the need to conduct duplicative clinical studies, preclinical studies, or nonclinical studies.
Medical product— In this section, the term “medical product” means a drug, as defined in subsection (g) of section 321 of this title, a device, as defined in subsection (h) of such section, or a biological product, as defined in section 351(i) of the Public Health Service Act [42 U.S.C. 262(i)].
Savings clause— Nothing in this section shall alter the criteria for evaluating the safety or effectiveness of a medical product under this chapter or under the Public Health Service Act [42 U.S.C. 201 et seq.].
Notes, amendments, and revision history
(June 25, 1938, ch. 675, § 569A, as added Pub. L. 112–144, title XI, § 1123, July 9, 2012, 126 Stat. 1113; amended Pub. L. 114–255, div. A, title III, § 3101(a)(2)(P), Dec. 13, 2016, 130 Stat. 1154.)
Editorial Notes
References in Text
The Public Health Service Act, referred to in subsec. (c), is act July 1, 1944, ch. 373, 58 Stat. 682, which is classified generally to chapter 6A (§ 201 et seq.) of Title 42, The Public Health and Welfare. For complete classification of this Act to the Code, see Short Title note set out under section 201 of Title 42 and Tables.
Amendments
2016—Subsec. (c). Pub. L. 114–255 inserted “or under the Public Health Service Act” before period at end.