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Federal Register · Proposed Rule · Mar 20, 2013
section 418 of the FD&C Act. … Written comments from the food industry supported such a control program (Ref. 69).
78 FR 17142Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Proposed Rule · Mar 13, 2003
complaints received during the marketing period. … Longer compliance periods. Lengthening the compliance period would provide regulatory relief for small entities.
68 FR 12158Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Proposed Rule · Jun 7, 1995
If FDA does not initiate such a proceeding, section 515(b)(3) of the act provides that FDA shall, after the close of the [[Page 30033]] comment period on the proposed rule and consideration of any comments … The difficulty was attributed to two factors: the large mass of the file, and the air trapped in the deep trough since air is a poor heat conductor (Ref. 5).
60 FR 30032Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Notice · Aug 20, 2009
Air Act, Public Law No. 101-549 (November 15, 1990). … At the public workshop, FDA will provide relevant background information, including a brief summary of the Montreal Protocol, the Clean Air Act, and the epinephrine final rule.
74 FR 42080Health and Human Services DepartmentFood and Drug AdministrationSanitary Transportation of Human and Animal Food
Federal Register · Rule · Apr 6, 2016
The commenter observes that railroads do not generally clean rail cars and do not track the cleaning of railcars. … period beyond the latest requirement.
81 FR 20092Health and Human Services DepartmentFood and Drug AdministrationMedical Gas Containers and Closures; Current Good Manufacturing Practice Requirements
Federal Register · Proposed Rule · Apr 10, 2006
Paperwork Reduction Act of 1995 VI. Environmental Impact VII. Effective Date VIII. Federalism IX. Request for Comments I. Background A. … b)(1) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. 321(g)(1) and 353(b)(1)).
71 FR 18039Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Proposed Rule · Mar 9, 1995
Proposed Replacement of CFC Propellants The Clean Air Act Amendments of 1990, Title VI (Pub. … Ozone-depleting substances covered by the Clean Air Act Amendments of 1990 include CFC's and hydrochlorofluorocarbons.
60 FR 13014Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Jun 25, 2007
Although the proposed rule's comment period was scheduled to end on June 11, 2003, in the Federal Register of May 19, 2003 (68 FR 27008), we extended the comment period to August 11, 2003. … (Comment 103) Several comments interpret proposed § 111.20(d)(4) as requiring fans and air-blowing equipment.
72 FR 34752Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Rule · Sep 17, 2015
Some comments agree that it is important that these food-contact surfaces are clean and sanitary when used, but because storage of equipment and utensils could be for an extended period of time, the comments … Proposed § 117.40(g)—Compressed Air or Other Gases We proposed no revisions to the requirement that compressed air or other gases mechanically introduced into food or used to clean food-contact surfaces
80 FR 55908Health and Human Services DepartmentFood and Drug AdministrationPerformance Standard for the Infant Apnea Monitor
Federal Register · Proposed Rule · Feb 21, 1995
comments regarding this proposal. … Sec. 896.57 Air mattress warning. Air mattresses shall be permanently labeled with the warning: ``Inflate only with room air, do NOT use pure oxygen''.
60 FR 9762Health and Human Services DepartmentFood and Drug AdministrationFederal Register · Proposed Rule · Nov 8, 2007
Background Under the Clean Air Act, FDA, in consultation with the Environmental Protection Agency, is required to determine whether an FDA-regulated product that releases an ODS is an essential use … Extension of the Comment Period for the Proposed Rule FDA is extending the comment period for the proposed rule to December 19, 2007.
72 FR 63141Health and Human Services DepartmentFood and Drug AdministrationStandards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption
Federal Register · Proposed Rule · Jan 16, 2013
We seek comment on these proposed implementation periods. … We seek comment on the proposed waiting period.
78 FR 3504Health and Human Services DepartmentFood and Drug AdministrationFederal 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 · Oct 27, 1999
(the act). … (the act).
64 FR 57893Health and Human Services DepartmentFood and Drug 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 AdministrationFederal 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 · 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 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 AdministrationFood 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 Administration
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