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Federal Register · Proposed Rule · Jul 6, 1999
Paperwork Reduction Act of 1995 IX. Comments X. References I. Background A. … After the eggs are washed, they are dried with forced ambient air and then packed.
64 FR 36492Proposed RulePreliminary Regulatory Impact Analysis and Initial RegulatoryFederal Register · Proposed Rule · Apr 10, 1998
Section 4 of Executive Order 12889 states that any agency subject to the Administrative Procedure Act shall provide a 75-day comment period for any proposed technical regulation. … As a result, a 75-day comment period is not required for this proposed rule. VII. References 1.
63 FR 17744Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Jan 19, 2000
Comments on the Proposed Categorical Exclusions The NIH received one comment on its proposed categorical exclusions. CEQ did not provide any comments. … Actions taken to comply with requirements of applicable legislation or regulations ( e.g., meet emissions requirements established pursuant to Clean Air Act). 17.
65 FR 2977Health and Human Services DepartmentNational Institutes of HealthFederal Register · Notice · Aug 20, 1999
DATES: Written comments must be received on or before October 19, 1999. ADDRESSES: Address all comments concerning this notice to Joseph G. … Actions taken to comply with requirements of applicable legislation or regulations (e.g., meet emissions requirements established pursuant to Clean Air Act). 17.
64 FR 45558Health and Human Services DepartmentNational Institutes of HealthFederal Register · Notice · Jul 25, 2005
• Section 211.182—Specifies requirements for equipment cleaning records and the use log. … Thereafter, SOPs need to be periodically updated. A combined estimate is provided in table 1 of this document.
70 FR 42579Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Apr 28, 2008
CGMP Regulations for Finished Pharmaceuticals—21 CFR Parts 210 and 211 (OMB Control Number 0910-0139)—Extension Under section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C … FDA has the authority under section 701(a) of the act (21 U.S.C. 371(a)) to issue regulations for the efficient enforcement of the act regarding CGMP procedures for manufacturing, processing, and holding
73 FR 22951Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Feb 7, 2002
CGMP Regulations for Finished Pharmaceuticals—21 CFR Parts 210 and 211 (OMB Control No. 0910-0139)—Extension Under section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. … Section 211.56(c)—Use of suitable rodenticides, insecticides, fungicides, fumigating agents, and cleaning and sanitizing agents; 4. Section 211.67(b)—Cleaning and maintenance of equipment; 5.
67 FR 5825Health and Human Services DepartmentFood and Drug AdministrationNational Toxicology Program; Announcement of Intent To Conduct Toxicological Studies of 22 Chemicals
Federal Register · Uncategorized Document · Sep 12, 1994
DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service National Toxicology Program; Announcement of Intent To Conduct Toxicological Studies of 22 Chemicals Request for Comments: As part of … Cresols are on the list of Hazardous Air Pollutants in the Clean Air Act Amendments of 1990 and on the Superfund Priority List of Hazardous Substances.
Health and Human Services DepartmentPublic Health ServiceProposed Data Collections Submitted for Public Comment and Recommendations
Federal Register · Notice · May 4, 2004
In 1982, periodic sampling of drinking water sources began at Camp Lejeune to comply with regulations of the national Safe Drinking Water Act. … These chemicals are used as solvents to clean machinery and weapons and in dry cleaning operations.
69 FR 24602Health and Human Services DepartmentCenters for Disease Control and PreventionFederal Register · Notice · May 31, 2011
FDA has the authority under section 701(a) of the FD&C Act (21 U.S.C. 371(a)) to issue regulations for the efficient enforcement of the FD&C Act regarding CGMP procedures for manufacturing, processing, … Thereafter, SOPs need to be periodically updated. A combined estimate for routine maintenance of SOPs is provided in table 1 of this document.
76 FR 31342Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Sep 28, 2011
The FDA has the authority under Section 701(a) of the FD&C Act (21 U.S.C. 371(a)) to issue regulations for the efficient enforcement of the FD&C Act regarding CGMP procedures for manufacturing, processing … Thereafter, SOPs need to be periodically updated. A combined estimate for routine maintenance of SOPs is provided in table 1 of this document.
76 FR 60052Health and Human Services DepartmentFood and Drug AdministrationUnified Agenda of Federal Regulatory and Deregulatory Actions
Federal Register · Proposed Rule · Jun 18, 2015
Availability 09/03/13 78 FR 54197 Framework Document Comment Period End 10/18/13 Preliminary Analysis 11/20/14 79 FR 69066 Preliminary Analysis Comment Period End 01/20/15 … Timetable: Action Date FR Cite NPRM and Notice of Public Meeting Date 03/23/15 02/09/15 80 FR 7082 NPRM Comment Period End 04/10/15 NPRM Comment Period Extended
80 FR 35012Energy DepartmentHealth and Human Services DepartmentFederal Register · Notice · Jan 7, 1999
Chief Financial Officer Act. … During this 180-day period, we will publish a separate Federal Register notice announcing the initiation of an extensive 60-day agency review and public comment period on these requirements.
64 FR 1025Health and Human Services DepartmentHealth Care Finance AdministrationFederal Register · Notice · Mar 28, 2005
CGMP Regulations for Finished Pharmaceuticals—21 CFR Parts 210 and 211 (OMB Control Number 0910-0139)—Extension Under section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the act) (21 … • Section 211.182—Specifies requirements for equipment cleaning records and the use log.
70 FR 15628Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · May 16, 2002
DATES: Submit written comments on the collection of information by June 17, 2002. … In the Federal Register of February 7, 2002 (67 FR 5825), the agency requested comments on the proposed collection of information. There were no comments received.
67 FR 34939Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Jun 6, 1997
However, as permitted by section 520(l)(5)(C) of the act, in the Federal Register of November 30, 1992 (57 FR 56586), the agency published a notice extending the period for issuing such regulations until … aids and accessory cleaning pads).
62 FR 31118Health and Human Services DepartmentFood and Drug AdministrationProposed Collection; 60-Day Comment request: Gulf Long-Term Follow-Up Study (GuLF STUDY)
Federal Register · Notice · Nov 7, 2013
requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Institute of Environmental Health Sciences … Comment Due Date: Comments regarding this information collection are best assured of having their full effect if received within 60 days of the date of this publication.
78 FR 66945Health and Human Services DepartmentNational Institutes of HealthEffective Date of Requirement for Premarket Approval for Blood Lancets
Federal Register · Proposed Rule · Mar 3, 2016
Section 515(b)(3) of the FD&C Act provides that FDA shall, after the close of the comment period on the proposed order, consideration of any comments received, and a meeting of a device classification … FDA cautions that under section 515(d)(1)(B)(i) of the FD&C Act, the Agency may not enter into an agreement to extend the review period for a PMA beyond 180 days unless the Agency finds that “. . . the
81 FR 11151Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Jul 17, 2019
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.
84 FR 34191Health and Human Services DepartmentFood and Drug AdministrationMedical Devices; Reprocessed Single-Use Devices; Requirement for Submission of Validation Data
Federal Register · Rule · Sep 25, 2006
days after the comment period on this direct final rule ends. … The comment period for this direct final rule runs concurrently with the comment period of the companion proposed rule.
71 FR 55729Health and Human Services DepartmentFood and Drug Administration
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