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Registration of Food Facilities Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002; Reopening of Comment Period
Federal Register · Rule · Apr 14, 2004
(Bioterrorism Act). … The agency will address comments on the identified set of issues that are received during this reopened comment period and were received during the previous comment period that closed on December 24, 2003
69 FR 19766Health and Human Services DepartmentFood and Drug Administration
Prior Notice of Imported Food Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002; Reopening of Comment Period
Federal Register · Rule · Apr 14, 2004
ACTION: Interim final rule; reopening of comment period. … the comment period for an additional 30 days in March 2004.
69 FR 19763Health and Human Services DepartmentFood and Drug Administration
Prior Notice of Imported Food Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002; Extension of Comment Period
Federal Register · Rule · May 18, 2004
ACTION: Interim final rule; extension of comment period. … We will address comments received during the entire reopened comment period and the previous comment period that closed on December 24, 2003, and will confirm or amend the IFR in a final rule.
69 FR 28060Health and Human Services DepartmentFood and Drug Administration
Use of Ozone-Depleting Substances
Federal Register · Rule · Oct 26, 2016
Air Act. … under the Clean Air Act.
81 FR 74298Health and Human Services DepartmentFood and Drug Administration
Use of Ozone-Depleting Substances; Essential-Use Determinations
Federal Register · Rule · Jul 24, 2002
However, FDA is changing the regulation to conform to the authority delegated to it under the Clean Air Act. FDA notes that EPA is responsible for enforcement of the Clean Air Act. … The Clean Air Act then prevents marketing of those ODS-containing products. The use of stockpiled CFCs is governed by the Clean Air Act.
67 FR 48370Health and Human Services DepartmentFood and Drug Administration
Use of Ozone-Depleting Substances; Removal of Essential Use Designations
Federal Register · Rule · Dec 7, 2006
Air Act. … Therefore, under the Federal Food, Drug, and Cosmetic Act, the Clean Air Act, and under authority delegated to the Commissioner of Food and Drugs, after consultation with the Administrator of the Environmental
71 FR 70870Health and Human Services DepartmentFood and Drug Administration
Use of Ozone-Depleting Substances; Removal of Essential-Use Designations
Federal Register · Rule · Apr 4, 2005
Under the Clean Air Act, a use of an ODS is either essential or it is not. … Air Act.
70 FR 17168Health and Human Services DepartmentFood and Drug Administration
Warning Statements for Products Containing or Manufactured With Chlorofluorocarbons and Other Ozone-Depleting Substances
Federal Register · Rule · May 3, 1996
The Clean Air Act requires that the warning labels be on all products containing or manufactured with CFC's on or after May 15, 1993. … For this interim rule, FDA finds that notice and comment procedures would be impracticable for a CFC warning statement requirement because the Clean Air Act requires such warning statements to be placed
61 FR 20096Warning Statements for Products Containing or Manufactured WithHealth and Human Services Department
Use of Ozone-Depleting Substances; Removal of Essential-Use Designation (Flunisolide, etc.)
Federal Register · Rule · Apr 14, 2010
The 1990 Amendments to the Clean Air Act In 1990, Congress amended the Clean Air Act to, among other things, better protect stratospheric ozone (Public Law No. 101-549, November 15, 1990) (the 1990 … Section 614(b) of the Clean Air Act provides that, in the case of a conflict between any provision of the Clean Air Act and any provision of the Montreal Protocol, the more stringent provision will govern
75 FR 19213Health and Human Services DepartmentFood and Drug Administration
Medical Gas Containers and Closures; Current Good Manufacturing Practice Requirements
Federal Register · Rule · Nov 18, 2016
(Comment 5) Some comments express concerns with FDA's proposal to add medical air to the list of gases at § 201.161(a) without providing a warning statement specific to medical air. … (Comment 25) FDA received several comments that the 60-day time period proposed for implementation of the proposed rule is insufficient.
81 FR 81685Health and Human Services DepartmentFood and Drug Administration
National Institutes of Health Training Grants
Federal Register · Rule · Oct 24, 1996
, as amended, and section 103(h)(2) of the Clean Air Act, as amended. … NIH also needs to provide regulations for training grants authorized by section 901 of the Clean Air Act Amendments of 1990, Public Law 101-549, which amended section 103(h)(2) of the Clean Air Act.
61 FR 55110Health and Human Services Department
Standards of Care for Chimpanzees Held in the Federally Supported Chimpanzee Sanctuary System
Federal Register · Rule · Oct 10, 2008
The NPRM provided for a 60-day public comment period. In December 2007, the CHIMP Act was amended by the “Chimp Haven is Home Act” (Pub. … (Comments) Three commenters suggested (1) the reference to a cleaning schedule for indoor enclosures be changed to read “Indoor primary enclosures must be cleaned as often as required to maintain a clean
73 FR 60410Health and Human Services Department
Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases
Federal Register · Rule · Jun 18, 2024
(Comment 36) One comment suggests revising § 213.182 to state that cleaning and maintenance is performed on a periodic basis or when there is suspected contamination and is not associated with a batch … (Comment 63) One comment maintains that entering a specific percentage of oxygen in the distribution records for each medical air cylinder is not necessary, because medical air contains a range of oxygen
89 FR 51738Health and Human Services DepartmentFood and Drug Administration
Use of Ozone-Depleting Substances; Removal of Essential-Use Designation (Epinephrine)
Federal Register · Rule · Nov 19, 2008
The 1990 Amendments to the Clean Air Act In 1990, Congress amended the Clean Air Act to, among other things, better protect stratospheric ozone (Public Law No. 101-549, November 15, 1990) (the 1990 … Section 614(b) of the Clean Air Act provides that, in the case of a conflict between any provision of the Clean Air Act and any provision of the Montreal Protocol, the more stringent provision will govern
73 FR 69532Health and Human Services DepartmentFood and Drug Administration
Temperature-Indicating Devices; Thermally Processed Low-Acid Foods Packaged in Hermetically Sealed Containers
Federal Register · Rule · Mar 3, 2011
(Comment 28) One comment suggested that the statement that air-operated temperature controllers should have adequate filter systems to ensure a supply of clean, dry air is misplaced in the regulations … Air-operated temperature controllers should have adequate filter systems to ensure a supply of clean, dry air.
76 FR 11892Health and Human Services DepartmentFood and Drug Administration
Approval Tests and Standards for Air-Purifying Particulate Respirators
Federal Register · Rule · Apr 14, 2020
Issuance of an Interim Final Rule With Immediate Effective Date Rulemaking under the Administrative Procedure Act (APA) generally requires a public notice and comment period and consideration of the submitted … (1) Powered air-purifying particulate respirators utilize a blower to move the ambient air through the air-purifying filter elements (filters) to remove particulate contaminants and deliver clean air
85 FR 20598Health and Human Services Department
Use of Ozone-Depleting Substances; Removal of Essential Use Designations; Confirmation of Effective Date
Federal Register · Rule · Apr 27, 2007
comment period. … Therefore, under the Federal Food, Drug, and Cosmetic Act, the Clean Air Act, and under authority delegated to the Commissioner of Food and Drugs, after consultation with the Administrator of the Environmental
72 FR 20942Health and Human Services DepartmentFood and Drug Administration
Current Good Manufacturing Practices, Quality Control Procedures, Quality Factors, Notification Requirements, and Records and Reports, for Infant Formula
Federal Register · Rule · Feb 10, 2014
, and the period of time between cleaning and subsequent use of the equipment and utensils. … Another comment suggested that records should be required to document equipment cleaning but not cleaning of utensils.
79 FR 7934Health and Human Services DepartmentFood and Drug Administration
General Hospital and Personal Use Devices: Renaming of Pediatric Hospital Bed Classification and Designation of Special Controls for Pediatric Medical Crib; Classification of Medical Bassinet
Federal Register · Rule · Dec 19, 2016
Summary of Comments to the Proposed Rule FDA requested comments on the proposed rule (80 FR 60809), and the comment period closed on December 7, 2015. … The Agency received 11 comments on the proposed rule by the close of the comment period; some of the comments contained comments on more than one issue.
81 FR 91731Health and Human Services DepartmentFood and Drug Administration
World Trade Center Health Program Eligibility Requirements for Shanksville, Pennsylvania and Pentagon Responders
Federal Register · Rule · Mar 28, 2013
Issuance of an Interim Final Rule with Delayed Effective Date In most circumstances, the APA requires a public notice and comment period and consideration of the submitted comments prior to promulgation … In compliance with the requirement of section 3506(c)(2)(A) of the PRA for opportunity for public comment on proposed data collection projects, CDC will publish periodic summaries of proposed projects.
78 FR 18855Health and Human Services Department

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