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Federal Register · Notice · Jun 15, 2010
Such delays would jeopardize project completion and related jobs in remote areas including Alaska villages where the only means of transporting such components is by air. … For many years, the IHS and the Environmental Protection Agency's (EPA) Clean Water Act lndian Set Aside and Drinking Water Infrastructure Grants-Tribal Set Aside programs jointly funded water infrastructure
75 FR 33818Health and Human Services DepartmentIndian Health ServiceRequirements Related to Surprise Billing
Federal Register · Rule · Aug 26, 2022
the open negotiation period. … the open negotiation period.
87 FR 52618Treasury DepartmentInternal Revenue ServiceFederal Register · Notice · Mar 16, 2012
L. 105-115) amended section 514 of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 360d). … It is only necessary to send one set of comments. Identify comments with the docket number found in brackets in the heading of this document.
77 FR 15765Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Oct 7, 2022
(FD&C Act) regarding safety, identity, strength, quality, and purity and are issued under the provisions of the Food and Drug Administration Modernization Act of 1997 (FDAMA) (Pub. … Five comments were received and are summarized here.
87 FR 61070Health and Human Services DepartmentFood and Drug AdministrationAgency Forms Undergoing Paperwork Reduction Act Review
Federal Register · Notice · Jul 7, 2023
CDC did not receive comments related to the previous notice This notice serves to allow an additional 30 days for public and affected agency comments. … State BRFSS Coordinators submit de-identified data files to CDC on a monthly or quarterly basis for cleaning and weighting.
88 FR 43353Health and Human Services DepartmentCenters for Disease Control and PreventionFederal Register · Notice · Mar 27, 2013
Under section 701(a) of the FD&C Act (21 U.S.C. 371(a)), FDA is authorized to issue regulations for the efficient enforcement of the FD&C Act. … Records are maintained on file at each farm site and examined there periodically by FDA inspectors.
78 FR 18605Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Apr 7, 2022
(FD&C Act) regarding safety, identity, strength, quality, and purity and are issued under the provisions of the Food and Drug Administration Modernization Act of 1997 (FDAMA) (Pub. … Annual Recordkeeping Incoming Acceptance Tests Records (§§ 212.20(c), 212.40(a) and (b)) 23 24 552 0.5 276 Annual Recordkeeping Batch Testing (creating testing records for sterility, periodic
87 FR 20420Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Aug 1, 2014
Medical Device Labeling Regulations—21 CFR 800, 801, and 809 (OMB Control Number 0910-0485)—Extension Section 502 of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 352), among other … Section 801.410(f) requires that the results of impact tests and description of the test method and apparatus be retained for a period of 3 years.
79 FR 44782Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · May 2, 2014
ACTION: Final rule with comment period. … This final rule with comment period adopts changes to the CLIA regulations to implement the TEST Act. 2. Summary of the Major Provisions a.
79 FR 25436Health and Human Services DepartmentCenters for Medicare & Medicaid ServicesAgency Forms Undergoing Paperwork Reduction Act Review
Federal Register · Notice · Sep 18, 2026
CDC received three public comments related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments. … for Disease Control and Prevention (CDC) is requesting a Revision of a currently approved information collection request (ICR) titled The STI Surveillance Network (SSuN) and approval for an additional period
91 FR 59137Health and Human Services DepartmentCenters for Disease Control and PreventionFederal Register · Proposed Rule · Apr 22, 1996
Beginning 14 days after close of the comment period, comments will be available for public inspection in Room 2218, 330 C Street, S.W., Washington, D.C. 20201, Monday through Friday between the hours of … (d) Probationary period.
61 FR 17754Health and Human Services DepartmentChildren and Families AdministrationPremarket Tobacco Product Applications and Recordkeeping Requirements
Federal Register · Proposed Rule · Sep 25, 2019
and the opportunity to submit comments. … FDA requests public comments on its interpretation of 910(d)(1)(A) of the FD&C Act.
84 FR 50566Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Mar 26, 2001
periods. … of 1972 (16 U.S.C. §§ 1451 et seq.); (f) conformity of Federal actions to State (Clean Air) Implementation Plans under Section 176(c) of the Clean Air Act of 1955, as amended (42 U.S.C. §§ 7401 et seq
66 FR 16556Health and Human Services DepartmentChildren and Families AdministrationFederal Register · Notice · Feb 22, 2018
Medical Device Labeling Regulations—21 CFR parts 800, 801, and 809 OMB Control Number 0910-0485—Extension Section 502 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 352), among other … Section 801.410(f) requires that the results of impact tests and description of the test method and apparatus be retained for a period of 3 years.
83 FR 7728Health and Human Services DepartmentFood and Drug AdministrationProposed Data Collection Submitted for Public Comment and Recommendations
Federal Register · Notice · Jul 5, 2022
ACTION: Notice with comment period. … on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995.
87 FR 39839Health and Human Services DepartmentCenters for Disease Control and PreventionFederal Register · Notice · Sep 27, 2010
ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk … DSHEA, among other things, amended the Federal Food, Drug, and Cosmetic Act (the FD&C Act) by adding section 402(g) of the FD&C Act (21 U.S.C. 342(g)).
75 FR 59266Health and Human Services DepartmentFood and Drug AdministrationProposed Data Collection Submitted for Public Comment and Recommendations
Federal Register · Notice · Jan 8, 2025
ACTION: Notice with comment period. … on a proposed information collection, as required by the Paperwork Reduction Act of 1995.
90 FR 1493Health and Human Services DepartmentCenters for Disease Control and PreventionMedicare Program: Changes to the Medicare Claims Appeal Procedures
Federal Register · Rule · Dec 9, 2009
Comment: Two commenters recommended that the term “non-clean claim” be defined. … Section 1869(a)(2)(A) of the Act, in conjunction with sections 1816(c)(2) and 1842(c)(2) of the Act, establishes that, on all claims other than clean claims, the initial determination shall be concluded
74 FR 65296Health and Human Services DepartmentCenters for Medicare & Medicaid ServicesElectronic Products; Performance Standard for Diagnostic X-Ray Systems and Their Major Components
Federal Register · Rule · Jun 10, 2005
Act (PHS Act) (42 U.S.C. 201 et seq. ) to chapter V of the act (21 U.S.C. 301 et seq. ). … No additional information was received on this topic during the comment period.
70 FR 33998Health and Human Services DepartmentFood and Drug Administration2018 National Health Interview Survey Questionnaire Redesign
Federal Register · Notice · Oct 7, 2016
ACTION: Notice with comment period. … The periodicity of rotating content will be established several years in advance.
81 FR 69827Health and Human Services DepartmentCenters for Disease Control and Prevention
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