3.0.0 4056 2019-11-15T21:15:49Z 2019-11-15T21:15:49Z House H HR 2012-02-16 112 From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]By Mr. BILBRAY:H.R. 4056.Congress has the power to enact this legislation pursuantto the following:Article VI, Clause 2: This Constitution, and the Laws ofthe United States which shall be made in Pursuance thereof;and all Treaties made, or which shall be made, under theAuthority of the United States, shall be the supreme Law ofthe Land; and the Judges in every State shall be boundthereby, any Thing in the Constitution or Laws of any Stateto the Contrary notwithstanding.[Page H902]]]> hsif00 Energy and Commerce Committee House Standing Referred to 2012-02-16T15:03:00Z 2012-02-16 Referred to the House Committee on Energy and Commerce. IntroReferral H11100 2 House floor actions hsif00 Energy and Commerce Committee 2012-02-16 Introduced in House IntroReferral Intro-H 9 Library of Congress 2012-02-16 Introduced in House IntroReferral 1000 9 Library of Congress B000461 Rep. Bilbray, Brian P. [R-CA-50] BRIAN BILBRAY R CA P. 50 N D000598 Rep. Davis, Susan A. [D-CA-53] SUSAN DAVIS D CA A. 53 2012-02-16 True L000274 Rep. Lewis, Jerry [R-CA-41] JERRY LEWIS R CA 41 2012-02-16 True R000487 Rep. Royce, Edward R. [R-CA-40] ED ROYCE R CA 40 2012-02-16 True C000059 Rep. Calvert, Ken [R-CA-44] KEN CALVERT R CA 44 2012-02-16 True B001228 Rep. Bono Mack, Mary [R-CA-45] MARY BONO MACK R CA 45 2012-02-16 True H001048 Rep. Hunter, Duncan D. [R-CA-52] Duncan Hunter R CA D. 52 2012-02-16 True Health Drug safety, medical device, and laboratory regulation Federal preemption Government studies and investigations Intergovernmental relations Manufacturing Retail and wholesale trades State and local government operations Health 00 2012-02-16 Introduced in House 2012-06-19T14:12:48Z Science and Technology Regulatory Relief Act of 2012 - Amends the Federal Food, Drug, and Cosmetic Act to prohibit a state or political subdivision from conducting or requiring an inspection of a factory, warehouse, or establishment in which a drug or device is manufactured, processed, packed, or held by a manufacturer or wholesale distributor for introduction into interstate commerce, or after such introduction, for purposes of verifying compliance with such Act, Public Health Service Act requirements regarding the regulation of biological products, or any similar requirements established pursuant to state law.

Makes exceptions for such an inspection if: (1) the state or subdivision makes a determination that a drug or device presents a threat of serious adverse health consequences or death; (2) the Secretary of Health and Human Services (HHS) orders a recall of a drug, biological product, or device manufactured, processed, packed, or held at the factory, warehouse, or establishment; or (3) the Secretary requests or authorizes the state to conduct or require the inspection.

]]> Science and Technology Regulatory Relief Act of 2012 Short Titles as Introduced Science and Technology Regulatory Relief Act of 2012 Display Title Science and Technology Regulatory Relief Act of 2012 Official Title as Introduced To amend the Federal Food, Drug, and Cosmetic Act to prevent a State or political subdivision thereof from conducting or requiring duplicative inspections of establishments in which a drug or device is manufactured, processed, packed, or held by a manufacturer or wholesale distributor of the drug or device. Introduced in House 2012-02-16T05:00:00Z https://www.govinfo.gov/content/pkg/BILLS-112hr4056ih/xml/BILLS-112hr4056ih.xml 2012-02-16 Referred to the House Committee on Energy and Commerce. text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. Congressional Research Service, Library of Congress This file contains bill summaries and statuses for federal legislation. A bill summary describes the most significant provisions of a piece of legislation and details the effects the legislative text may have on current law and federal programs. Bill summaries are authored by the Congressional Research Service (CRS) of the Library of Congress. As stated in Public Law 91-510 (2 USC 166 (d)(6)), one of the duties of CRS is "to prepare summaries and digests of bills and resolutions of a public general nature introduced in the Senate or House of Representatives". For more information, refer to the User Guide that accompanies this file.