United States Government Publishing Office publisher pbl distributor dst United States National Archives and Records Administration Office of the Federal Register author aut Government Organization text government publication eng FR Regulatory Information 2017_register executive 2018-10-24 article Proposed Rules D09002ee1c7f100f0 D09002ee1c7f1013d United States Department of Health and Human Services originator org United States Government Agency or Subagency United States Food and Drug Administration originator org United States Government Agency or Subagency As part of the implementation of Executive Order 13771 entitled, "Reducing Regulation and Controlling Regulatory Costs," and Executive Order 13777 entitled, "Enforcing the Regulatory Reform Agenda," the Food and Drug Administration (FDA, Agency, or we) is seeking comments and information from interested parties to help FDA identify existing regulations and related paperwork requirements that could be modified, repealed, or replaced, consistent with the law, to achieve meaningful burden reduction while allowing us to achieve our public health mission and fulfill statutory obligations. This document relates to general regulatory and information collection requirements that affect multiple FDA Centers and/or Offices. 82 FR 42506 https://www.govinfo.gov/app/details/FR-2017-09-08/2017-19047 2017-19047 fr08se17-18 4164-01-P Docket No. FDA-2017-N-5093 https://www.govinfo.gov/app/details/FR-2017-09-08/2017-19047 https://www.govinfo.gov/content/pkg/FR-2017-09-08/html/2017-19047.htm https://www.govinfo.gov/content/pkg/FR-2017-09-08/pdf/2017-19047.pdf 3 p. 42506 42508 82 FR 42506 Title 21 Chapter 21 CFR Chapter Review of Existing General Regulatory and Information Collection Requirements of the Food and Drug Administration; Federal Register Vol. 82, Issue PRORULE 2017-19047 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 2017-12-07 Docket No. FDA-2017-N-5093 4164-01-P 2017-19047 Request for comments and information.

As part of the implementation of Executive Order 13771 entitled, "Reducing Regulation and Controlling Regulatory Costs," and Executive Order 13777 entitled, "Enforcing the Regulatory Reform Agenda," the Food and Drug Administration (FDA, Agency, or we) is seeking comments and information from interested parties to help FDA identify existing regulations and related paperwork requirements that could be modified, repealed, or replaced, consistent with the law, to achieve meaningful burden reduction while allowing us to achieve our public health mission and fulfill statutory obligations. This document relates to general regulatory and information collection requirements that affect multiple FDA Centers and/or Offices.

Submit either electronic or written comments on this document by December 7, 2017. Megan Velez, Office of Policy, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993, 301-796-4830, megan.velez@fda.hhs.gov. Review of Existing General Regulatory and Information Collection Requirements of Food and Drug Administration , megan.velez@fda.hhs.gov https://www.ecfr.gov https://www.federalregister.gov/documents/2017/02/03/2017-02451/reducing-regulation-and-controlling-regulatory-costs https://www.federalregister.gov/documents/2017/03/01/2017-04107/enforcing-the-regulatory-reform-agenda https://www.gpo.gov/fdsys/pkg/FR-2015-09-18/pdf/2015-23389.pdf https://www.regulations.gov Vol. 82, no. 173 Office of the Federal Register, National Archives and Records Administration 2017-09-08 continuing daily deposited born digital 146 p. Table of Contents: AE 2.7: GS 4.107: AE 2.106: KF70.A2 https://www.govinfo.gov/app/details/FR-2017-09-08 P0b002ee19d731eff 0097-6326 0042-1219 0364-1406 769-004-00000-9 000582072 f:fr08se17 https://www.govinfo.gov/app/details/FR-2017-09-08 https://www.govinfo.gov/content/pkg/FR-2017-09-08/pdf/FR-2017-09-08.pdf https://www.govinfo.gov/content/pkg/FR-2017-09-08/xml/FR-2017-09-08.xml fdlp 42441 42577 DGPO 2018-10-24 2024-06-01 FR-2017-09-08 machine generated eng FR FR-2017-09-08 82 173