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Control of Communicable Disease; Foreign-Requirements for Importers of Nonhuman Primates (NHP)
Federal Register · Rule · Feb 15, 2013
life of an NHP and a period after death, as some commenters suggested. … -based animal acts to the same requirements for entry as foreign-based animal acts; all such NHPs will be subject to a quarantine period regardless of where the animals are based. M.
78 FR 11522Health and Human Services DepartmentChlorofluorocarbon Propellants in Self-Pressurized Containers; Addition to List of Essential Uses
Federal Register · Proposed Rule · Mar 1, 1996
EPA regulations implementing provisions of the Clean Air Act contain a general ban on the use of CFC's in pressurized dispensers (40 CFR 82.64(c) and 82.66(d)). … Section 601(8) of the Clean Air Act (42 U.S.C. 7671(8)) defines ``medical device'' as any device (as defined in the Federal Food, Drug, and Cosmetic Act), diagnostic product, drug (as defined in the Federal
61 FR 8002Health and Human Services DepartmentFederal Register · Notice · Jul 2, 2014
(the FD&C Act), in accordance with provisions added by the Drug Quality and Security Act (DQSA). … Procedures must be established that assign responsibility for and describe cleaning schedules, methods, equipment, and materials.
79 FR 37743Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Feb 13, 2003
SAMHSA, however, is seeking comment from the public on this guidance. … Examples of possible policy initiatives may include, but not be limited to, encouraging clean indoor air policies, increasing tobacco taxes, or formally supporting youth tobacco cessation programs.
68 FR 7384Health and Human Services DepartmentSubstance Abuse and Mental Health Services AdministrationChlorofluorocarbon Propellants in Self-Pressurized Containers; Addition to List of Essential Uses
Federal Register · Proposed Rule · Oct 17, 1995
EPA regulations implementing provisions of the Clean Air Act contain a general ban on the use of CFC's in pressurized dispensers, such as metered-dose inhalers (MDI's) (40 CFR 82.64(c) and 82.66(d)). … Section 601(8) of the Clean Air Act (42 U.S.C. 7671(8)) defines ``medical device'' as any device (as defined in the Federal Food, Drug, and Cosmetic Act), diagnostic product, drug (as defined in the Federal
60 FR 53725Health and Human Services DepartmentFood and Drug AdministrationChlorofluorocarbon Propellants in Self-Pressurized Containers; Addition to List of Essential Uses
Federal Register · Rule · Apr 9, 1996
EPA regulations implementing provisions of the Clean Air Act contain a general ban on the use of CFC's in pressurized dispensers, such as metered-dose inhalers (MDI's) (40 CFR 82.64(c) and 82.66(d)). … Section 601(8) of the Clean Air Act (42 U.S.C. 7671(8)) defines ``medical device'' as any device (as defined in the Federal Food, Drug, and Cosmetic Act), diagnostic product, drug (as defined in the Federal
61 FR 15699Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Jan 26, 2015
Comment: One commenter suggests that a 1-year period between revisions of fees schedules will not allow sufficient time for companies to plan. … clean breathing air (from a supply separate from the ambient air).
80 FR 3891Health and Human Services DepartmentFederal Register · Notice · Oct 27, 1999
(the act). … (the act).
64 FR 57893Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Mar 7, 2017
Follow the instructions for submitting comments. … The public comments indicated that (1) the proposed IDLH value was overprotective, (2) the data available for peracetic acid are of low quality, and (3) issues exist with the sampling and analysis of air
82 FR 12819Health and Human Services DepartmentCenters for Disease Control and PreventionFederal Register · Proposed Rule · May 9, 2013
Transmission of infectious diseases due to improper cleaning and disinfection would be mitigated through the requirement to provide instructions for cleaning and disinfection of the device that have been … FDA would expect sunlamp products marketed during the 1 year period to comply with all special controls by the time the period expires.
78 FR 27117Health and Human Services DepartmentFood and Drug AdministrationChlorofluorocarbon Propellants in Self-Pressurized Containers; Addition to List of Essential Uses
Federal Register · Rule · May 21, 1996
EPA regulations implementing provisions of the Clean Air Act contain a general ban on the use of CFC's in pressurized dispensers (40 CFR 82.64(c) and 82.66(d)). … Section 601(8) of the Clean Air Act (42 U.S.C. 7671(8)) defines ``medical device'' as any device (as defined in the Federal Food, Drug, and Cosmetic Act), diagnostic product, drug (as defined in the Federal
61 FR 25390Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Nov 24, 2004
Two comments requested a grace period of 1 to 2 years; one comment requested a 2-year implementation period; and another comment requested an extension of the compliance deadline to 1 year after publication … Where appropriate, you must provide for the following control activities or systems: (1) Temperature and humidity controls; (2) Ventilation and air filtration; (3) Cleaning and disinfecting of rooms
69 FR 68612Health and Human Services DepartmentFood and Drug AdministrationSanitary Transportation of Human and Animal Food
Federal Register · Proposed Rule · Feb 5, 2014
We request comment on whether any other persons should be subject to this proposed rule under the authority provided by section 416(b) of the FD&C Act. … In addition, comments to the 2010 ANPRM stated that dry trailers used to haul non-refrigerated, fully packaged food items are swept or vacuum cleaned before being offered for loading.
79 FR 7006Health and Human Services DepartmentFood and Drug AdministrationInitiatives by Organizations to Strengthen National Tobacco Control Activities in the United States
Federal Register · Notice · Jul 8, 1997
[[Page 36552]] Current scientific and program findings support the implementation of the following tobacco control programs: Clean Indoor Air protection from ETS in buildings, restaurants, schools … Environmental tobacco smoke (clean indoor air protection). c. Counter advertising and promotion (advertising strategies to counter the promotion of tobacco use). d.
62 FR 36550Health and Human Services DepartmentCenters for Disease Control and PreventionFood Labeling: Health Claims; Soluble Dietary Fiber From Certain Foods and Coronary Heart Disease
Federal Register · Rule · Dec 23, 2005
Section 403(r)(7) of the act authorizes us to make proposed regulations issued under section 403(r) of the act effective upon publication pending consideration of public comment and publication of a final … FDA invites public comment on this interim final rule. The agency will consider modifications to this interim final rule based on comments made during the comment period.
70 FR 76150Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Jun 10, 2014
(f) * * * (4) Records, in accordance with § 106.30(f), on equipment cleaning, sanitizing, and maintenance that show the date and time of such cleaning, sanitizing, and maintenance and the production aggregate … number of each infant formula processed between equipment startup and shutdown for cleaning, sanitizing, and maintenance.
79 FR 33057Health and Human Services DepartmentFood and Drug AdministrationProposed Data Collection Submitted for Public Comment and Recommendations
Federal Register · Notice · Sep 30, 2015
(CDC), Department of Health and Human Services (HHS) ACTION: Notice with comment period. … on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995.
80 FR 58735Health and Human Services DepartmentAgency for Toxic Substances and Disease RegistryFederal Register · Notice · Mar 30, 2020
Background Section 204 of the Food and Drug Administration Modernization Act of 1997 (Pub. L. 105-115) amended section 514 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 360d). … Guide for Using a Force Tester to Evaluate the Performance of a Brush Part Designed to Clean the External Surface of a Medical Device ASTM F3276-19.
85 FR 17584Health and Human Services DepartmentFood and Drug AdministrationControl of Communicable Diseases; Foreign Quarantine: Importation of Dogs and Cats
Federal Register · Proposed Rule · Jul 10, 2023
Written comments on the proposed data collection requirements under the Paperwork Reduction Act must be received by September 8, 2023. … HHS/CDC will publish a final rule after the comment period that reflects any content changes made because of comments received. III. Background A.
88 FR 43978Health and Human Services DepartmentFederal Register · Proposed Rule · Aug 24, 2017
Air Act. … On June 29, 2015, FDA published a notice and request for comment concerning its tentative conclusion that these products are no longer an essential use under the Clean Air Act (80 FR 36937).
82 FR 40277Health and Human Services DepartmentOffice of the Secretary
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