August 27, 2007 – Federal Register Recent Federal Regulation Documents

Results 101 - 107 of 107
Off-Highway Vehicle Travel Management Plan
Document Number: 07-4164
Type: Notice
Date: 2007-08-27
Agency: Department of Agriculture, Forest Service
The Mt. Hood National Forest (Forest) will prepare an Environmental Impact Statement (EIS) to document and disclose the potential environmental effects of establishing and designating a system of roads, trails and areas for off-highway vehicles (OHV). The Proposed Action will change OHV access through much of the Forest in order to meet the intent of the Travel Management; Designated Routes and Areas for Motor Vehicle Use; Final Rule that was published on November 9, 2005 (70 FR 216). The Proposed Action focuses on travel management within six proposed OHV areas and motorized access to dispersed (undeveloped) camping. Within each area, specific OHV routes are proposed by motor vehicle class, and new trails are proposed for construction where they would create trail loop opportunities. A Forest Plan Amendment would be required to achieve the purpose and need, and implement the Proposed Action.
Houston District Advisory Council; Public Federal Meeting
Document Number: 07-4160
Type: Notice
Date: 2007-08-27
Agency: Small Business Administration, Agencies and Commissions
National Institute of Arthritis and Musculoskeletal and Skin Diseases; Notice of Closed Meeting
Document Number: 07-4158
Type: Notice
Date: 2007-08-27
Agency: Department of Health and Human Services, National Institutes of Health
Office of the Director, National Institutes of Health; Notice of Meeting
Document Number: 07-4157
Type: Notice
Date: 2007-08-27
Agency: Department of Health and Human Services, National Institutes of Health
Notice of Open Special Meeting of the Advisory Committee of the Export-Import Bank of the United States (Ex-Im Bank)
Document Number: 07-4154
Type: Notice
Date: 2007-08-27
Agency: Export-Import Bank of the United States, Export-Import Bank, Agencies and Commissions
The Advisory Committee was established by Public Law 98-181, November 30, 1983, to advise the Export-Import Bank on its programs and to provide comments for inclusion in the reports of the Export-Import Bank on its programs and to provide comments for inclusion in the reports of the Export-Import Bank of the United States to Congress. Time and Place: Wednesday, September 19, 2007 from 9 a.m. to 12 p.m. The meeting will be held at Ex-Im Bank in the Main Conference Room 1143, 811 Vermont Avenue, NW., Washington, DC 20571. Agenda: Agenda items include a short summary of the Bank's recent activities, plus presentations from the Finance & Government Team and the Labor & Agriculture Team of the 2007 Advisory Committee members. Public Participation: The meeting will be open to public participation, and the last 10 minutes will be set aside for oral questions or comments. Members of the public may also file written statement(s) before or after the meeting. If you plan to attend, a photo ID must be presented at the guard's desk as part of the clearance process into the building, and you may contact Teri Stumpf to be placed on an attendee list. If any person wishes auxiliary aids (such as a sign language interpreter) or other special accommodations, please contact, prior to September 5, 2007, Teri Stumpf, Room 1209, 811 Vermont Avenue, NW., Washington, DC 20571, Voice: (202) 565-3502 or TDD (202) 565-3377. Further Information: For further information, contact Teri Stumpf, Room 1209, 811 Vermont Ave., NW., Washington, DC 20571, (202) 565-3502.
Sunscreen Drug Products for Over-the-Counter Human Use; Proposed Amendment of Final Monograph
Document Number: 07-4131
Type: Proposed Rule
Date: 2007-08-27
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is issuing a proposed rule that would amend the final monograph (FM) for over-the-counter (OTC) sunscreen drug products as part of FDA's ongoing review of OTC drug products. This amendment addresses formulation, labeling, and testing requirements for both ultraviolet B (UVB) and ultraviolet A (UVA) radiation protection. FDA is issuing this proposed rule after considering public comments and new data and information that have come to FDA's attention. This rule proposes to lift the stays of 21 CFR 347.20(d) and 21 CFR Part 352 when FDA publishes a final rule based on this proposed rule.
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