February 13, 2012 – Federal Register Recent Federal Regulation Documents

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Freeport LNG Expansion, L.P. and FLNG Liquefaction, LLC; Application for Long-Term Authorization To Export Domestically Produced Liquefied Natural Gas to Non Free Trade Agreement Countries for a 25-Year Period
Document Number: 2012-3247
Type: Notice
Date: 2012-02-13
Agency: Department of Energy
The Office of Fossil Energy (FE) of the Department of Energy (DOE) gives notice of receipt of an application (Application), filed on December 19, 2011, by Freeport LNG Expansion, L.P. and FLNG Liquefaction, LLC (collectively, FLEX), requesting long-term, multi- contract authorization to export domestically produced liquefied natural gas (LNG) in an amount up to the equivalent of 511 Billion cubic feet (Bcf) of natural gas per year, which averages to 1.4 Bcf per day (Bcf/d), over a 25-year period, commencing on the earlier of the date of first export or eight years from the date the requested authorization is granted. The LNG would be exported from the Freeport LNG Terminal on Quintana Island near Freeport, Texas, to any country (1) with which the United States does not have a free trade agreement (FTA) requiring national treatment for trade in natural gas, (2) which has developed or in the future develops the capacity to import LNG via ocean-going carrier, and (3) with which trade is not prohibited by U.S. law or policy. The Application is filed independent of, and in addition to, FLEX's prior application filed with DOE/FE under Docket No. 10-161- LNG. This Application was filed under section 3 of the Natural Gas Act (NGA). Protests, motions to intervene, notices of intervention, and written comments are invited.
Dow Chemical Company; Dow Chemical TRIGA Research Reactor; Facility Operating License No. R-108
Document Number: 2012-3246
Type: Notice
Date: 2012-02-13
Agency: Nuclear Regulatory Commission, Agencies and Commissions
Disapproval and Promulgation of Air Quality Implementation Plans; Montana; Revisions to the Administrative Rules of Montana-Air Quality, Subchapter 7, Exclusion for De Minimis Changes
Document Number: 2012-3245
Type: Rule
Date: 2012-02-13
Agency: Environmental Protection Agency
EPA is taking final action to partially approve and partially disapprove State Implementation Plan (SIP) revisions and new rules as submitted by the State of Montana on June 25, 2010 and May 28, 2003. The revisions contain new rules in Subchapter 7 (Permit, Construction, and Operation of Air Contaminant Sources) that pertain to the issuance of Montana air quality permits, in addition to other minor administrative changes to other subchapters of the Administrative Rules of Montana (ARM). In this action, EPA is approving those portions of the rules that are approvable and disapproving those portions of the rules that are inconsistent with the Clean Air Act (CAA). This action is being taken under section 110 of the CAA.
Definitions and Abbreviations
Document Number: 2012-3244
Type: Rule
Date: 2012-02-13
Agency: Department of Agriculture, Rural Business-Cooperative Service, Rural Utilities Service
The Rural Business-Cooperative Service is amending its regulations for the Business and Industry Guaranteed Loan Program to clarify that the Agency guarantee does not cover default and penalty interest or late charges. The Agency's regulations are currently silent on this issue. However, it has always been the Agency's policy not to pay out additional cost for default interest, penalty interest, and late charges calculated and submitted on a final report of loss claim under the Loan Note Guarantee. The Agency does permit the lender to charge default interest with prior Agency approval. By defining ``interest'' in the definition section of the regulation and clarifying the Agency's policy as it relates to default interest, penalty interest, and late charge, this will avert any misunderstandings.
Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
Document Number: 2012-3243
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
Definitions and Abbreviations
Document Number: 2012-3242
Type: Proposed Rule
Date: 2012-02-13
Agency: Department of Agriculture, Rural Business-Cooperative Service, Rural Utilities Service
The Rural Business-Cooperative Service is amending its regulations for the Business and Industry Guaranteed Loan Program to clarify that the Agency guarantee does not cover default and penalty interest or late charges. The Agency's regulations are currently silent on this issue. However, it has always been the Agency's policy not to pay out additional cost for default interest, penalty interest, and late charges calculated and submitted on a final report of loss claim under the Loan Note Guarantee. The Agency does permit the lender to charge default interest with prior Agency approval. By defining ``interest'' in the definition section of the regulation and clarifying the Agency's policy as it relates to default interest, penalty interest, and late charge, this will avert any misunderstandings.
Notice of Segregation of Public Lands in the State of Arizona for the Restoration Design Energy Project-Agua Caliente Solar Energy Zone in Yuma County, AZ
Document Number: 2012-3241
Type: Notice
Date: 2012-02-13
Agency: Department of the Interior, Bureau of Land Management
The Bureau of Land Management (BLM) is segregating public lands located in the State of Arizona from all forms of appropriation under the public land laws, including the mining law, but excluding the mineral leasing or materials sale laws, for a period of up to 2 years. This is for the purpose of protecting potential sites for future solar energy development while they are being analyzed in the Restoration Design Energy Project (RDEP). The public lands contained in this segregation total approximately 20,776 acres in Yuma County.
Aviation Proceedings, Agreements Filed the Week Ending January 28, 2012
Document Number: 2012-3240
Type: Notice
Date: 2012-02-13
Agency: Department of Transportation, Office of the Secretary
Notice of Receipt of Complaint; Solicitation of Comments Relating to the Public Interest
Document Number: 2012-3237
Type: Notice
Date: 2012-02-13
Agency: International Trade Commission, Agencies and Commissions
Notice is hereby given that the U.S. International Trade Commission has received a complaint entitled Certain Mobile Electronic Devices Incorporating Haptics, DN 2875; the Commission is soliciting comments on any public interest issues raised by the complaint or complainant's filing under section 210.8(b) of the Commission's Rules of Practice and Procedure (19 CFR 210.8(b)).
Receipt of Applications for Endangered Species Permits
Document Number: 2012-3236
Type: Notice
Date: 2012-02-13
Agency: Fish and Wildlife Service, Department of the Interior
We, the U.S. Fish and Wildlife Service, invite the public to comment on the following applications to conduct certain activities with endangered species. With some exceptions, the Endangered Species Act (ESA) prohibits activities with listed species unless a Federal permit is issued that allows such activities. The ESA requires that we invite public comment before issuing these permits.
Draft Guidance for Industry on Bioequivalence Recommendations for Rifaximin Tablets; Availability
Document Number: 2012-3234
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing the availability of two draft guidances for industry entitled ``Bioequivalence Recommendations for Rifaximin,'' one for the 200- milligram (mg) strength (rifaximin-200) and one for the 550-mg strength (rifaximin-550). The recommendations provide specific guidance on the design of bioequivalence (BE) studies to support abbreviated new drug applications (ANDAs) for rifaximin tablets.
Draft Guidance for Industry on Bioequivalence Recommendation for Nitroglycerin Metered Spray/Sublingual Products and Metered Aerosol/Sublingual Products; Availability
Document Number: 2012-3233
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing the availability of two draft guidances for industry entitled ``Bioequivalence Recommendations for Nitroglycerin,'' one for nitroglycerin metered spray/sublingual products and one for nitroglycerin metered aerosol/sublingual products. The recommendations provide specific guidance on the design of bioequivalence (BE) studies to support abbreviated new drug applications (ANDAs) for these products. The draft guidances are revised versions of previously published draft guidances on the subject.
Determination That WILPO (phentermine hydrochloride) Tablets, 8 Milligrams, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
Document Number: 2012-3232
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) has determined that WILPO (phentermine hydrochloride) Tablets, 8 Milligrams (mg), was not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to approve Abbreviated New Drug Applications (ANDAs) for phentermine hydrochloride tablets, 8 mg, if all other legal and regulatory requirements are met.
Pacific Fishery Management Council; Public Meetings
Document Number: 2012-3231
Type: Notice
Date: 2012-02-13
Agency: Department of Commerce, National Oceanic and Atmospheric Administration
The Pacific Council and its advisory entities will hold public meetings.
Draft Guidance for Industry on Heparin for Drug and Medical Device Use; Monitoring Crude Heparin for Quality; Availability
Document Number: 2012-3229
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled ``Heparin for Drug and Medical Device Use: Monitoring Crude Heparin for Quality.'' This draft guidance is intended to alert manufacturers of active pharmaceutical ingredients (APIs), pharmaceutical and medical device manufacturers of finished products, and others to the potential risk of crude heparin contamination.
Revised Medical Criteria for Evaluating Visual Disorders
Document Number: 2012-3226
Type: Proposed Rule
Date: 2012-02-13
Agency: Social Security Administration, Agencies and Commissions
We propose to revise and reorganize the criteria in the Listing of Impairments (listings) that we use to evaluate cases involving visual disorders in adults and children under titles II and XVI of the Social Security Act (Act). The proposed revisions reflect our program experience and address adjudicator questions we have received since we last revised these criteria in 2006. These proposed revisions reflect guidance we have issued in response to adjudicator questions and will ensure more timely adjudication of claims in which we evaluate visual impairments that involve a loss of visual acuity or loss of visual fields.
Determination That KAPVAY (Clonidine Hydrochloride) Extended-Release Tablets, 0.2 Milligram, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
Document Number: 2012-3223
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) has determined that KAPVAY (clonidine hydrochloride) Extended-Release Tablets, 0.2 milligram (mg), was not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to approve abbreviated new drug applications (ANDAs) for clonidine hydrochloride extended- release tablets, 0.2 mg, if all other requirements are met.
Determination That JENLOGA (Clonidine Hydrochloride) Extended-Release Tablets, 0.1 Milligram and 0.2 Milligram, Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness
Document Number: 2012-3222
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) has determined that JENLOGA (clonidine hydrochloride) Extended-Release Tablets, 0.1 milligram (mg) and 0.2 mg, were not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to approve abbreviated new drug applications (ANDAs) for clonidine hydrochloride extended-release tablets, 0.1 mg and 0.2 mg, if all other requirements are met.
Antiparasitic Drug Use and Resistance in Ruminants and Equines; Public Meeting; Request for Comments
Document Number: 2012-3221
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
Proposed Collection; Comment Request
Document Number: 2012-3220
Type: Notice
Date: 2012-02-13
Agency: Securities and Exchange Commission, Agencies and Commissions
Certain Strollers and Playards; Decision Not To Review an Initial Determination Terminating the Investigation on the Basis of a Settlement Agreement
Document Number: 2012-3212
Type: Notice
Date: 2012-02-13
Agency: International Trade Commission, Agencies and Commissions
Notice is hereby given that the U.S. International Trade Commission has determined not to review the presiding administrative law judge's initial determination (``ID'') (Order No. 11) granting a joint motion to terminate the above-captioned investigation on the basis of a settlement agreement.
Agency Information Collection Request; 60-Day Public Comment Request
Document Number: 2012-3210
Type: Notice
Date: 2012-02-13
Agency: Department of Health and Human Services
Suspension of Community Eligibility
Document Number: 2012-3209
Type: Rule
Date: 2012-02-13
Agency: Federal Emergency Management Agency, Department of Homeland Security
This rule identifies communities where the sale of flood insurance has been authorized under the National Flood Insurance Program (NFIP) that are scheduled for suspension on the effective dates listed within this rule because of noncompliance with the floodplain management requirements of the program. If the Federal Emergency Management Agency (FEMA) receives documentation that the community has adopted the required floodplain management measures prior to the effective suspension date given in this rule, the suspension will not occur and a notice of this will be provided by publication in the Federal Register on a subsequent date.
Waiver of Debt
Document Number: 2012-3208
Type: Notice
Date: 2012-02-13
Agency: Federal Emergency Management Agency, Department of Homeland Security
FEMA is providing notice of its implementation of the Disaster Assistance Recoupment Fairness Act of 2011 (Pub. L. 112-74) (DARFA). DARFA provides the Administrator of FEMA with the authority to waive certain debts arising from improper payments provided to disaster survivors for disasters declared between August 28, 2005, and December 31, 2010.
Alaska; Major Disaster and Related Determinations
Document Number: 2012-3207
Type: Notice
Date: 2012-02-13
Agency: Federal Emergency Management Agency, Department of Homeland Security
This is a notice of the Presidential declaration of a major disaster for the State of Alaska (FEMA-4054-DR), dated February 2, 2012, and related determinations.
Federal Radiological Preparedness Coordinating Committee
Document Number: 2012-3206
Type: Notice
Date: 2012-02-13
Agency: Federal Emergency Management Agency, Department of Homeland Security
The Federal Radiological Preparedness Coordinating Committee (FRPCC) is holding a public meeting on February 24, 2012 in Arlington, VA.
Utah; Major Disaster and Related Determinations
Document Number: 2012-3205
Type: Notice
Date: 2012-02-13
Agency: Federal Emergency Management Agency, Department of Homeland Security
This is a notice of the Presidential declaration of a major disaster for the State of Utah (FEMA-4053-DR), dated February 1, 2012, and related determinations.
Notice of permit applications received under the Antarctic Conservation Act of 1978
Document Number: 2012-3204
Type: Notice
Date: 2012-02-13
Agency: National Science Foundation, Agencies and Commissions
The National Science Foundation (NSF) is required to publish a notice of permit applications received to conduct activities regulated under the Antarctic Conservation Act of 1978. NSF has published regulations under the Antarctic Conservation Act at Title 45 Part 670 of the Code of Federal Regulations. This is the required notice of permit applications received.
Gastrointestinal Drugs Advisory Committee; Notice of Meeting
Document Number: 2012-3203
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
Final Flood Elevation Determinations
Document Number: 2012-3202
Type: Rule
Date: 2012-02-13
Agency: Federal Emergency Management Agency, Department of Homeland Security
Base (1% annual-chance) Flood Elevations (BFEs) and modified BFEs are made final for the communities listed below. The BFEs and modified BFEs are the basis for the floodplain management measures that each community is required either to adopt or to show evidence of being already in effect in order to qualify or remain qualified for participation in the National Flood Insurance Program (NFIP).
Alabama; Major Disaster and Related Determinations
Document Number: 2012-3200
Type: Notice
Date: 2012-02-13
Agency: Federal Emergency Management Agency, Department of Homeland Security
This is a notice of the Presidential declaration of a major disaster for the State of Alabama (FEMA-4052-DR), dated February 1, 2012, and related determinations.
Blood Products Advisory Committee; Cancellation
Document Number: 2012-3199
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The meeting of the Blood Products Advisory Committee scheduled for February 29, 2012 is cancelled. This meeting was announced in the Federal Register of January 30, 2012 (77 FR 4567). FDA intends to convene at a future date a public scientific workshop to discuss the evaluation of possible new plasma products manufactured following storage at room temperature for up to 24 hours.
Request for Notification From Consumer Organizations Interested in Participating in the Selection Process for Nominations for Voting and/or Nonvoting Consumer Representatives and Consumer Representatives on Public Advisory Committees or Panels
Document Number: 2012-3198
Type: Notice
Date: 2012-02-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is requesting that any consumer organizations interested in participating in the selection of voting and/or nonvoting consumer representatives to serve on its advisory committees or panels notify FDA in writing. FDA is also requesting nominations for voting and/or nonvoting consumer representatives to serve on advisory committees and/or panels for which vacancies currently exist or are expected to occur in the near future. Nominees recommended to serve as a voting or nonvoting consumer representative may either be self-nominated or may be nominated by a consumer organization. Nominations will be accepted for current vacancies and for those that will or may occur through February 2013.
Information Regarding General Licenses A and B Under the New Executive Order of February 5, 2012
Document Number: 2012-3197
Type: Notice
Date: 2012-02-13
Agency: Department of the Treasury, Office of Foreign Assets Control
The Department of the Treasury's Office of Foreign Assets Control (``OFAC'') is providing information regarding General Licenses A and B issued pursuant to the new Executive Order of February 5, 2012 (``Blocking Property of the Government of Iran and Iranian Financial Institutions'') (``new Executive Order'').
Agency Information Collection Activities: Announcement of Board Approval Under Delegated Authority and Submission to OMB
Document Number: 2012-3192
Type: Notice
Date: 2012-02-13
Agency: Federal Reserve System, Agencies and Commissions
Notice is hereby given of the final approval of proposed information collections by the Board of Governors of the Federal Reserve System (Board) under OMB delegated authority, as per 5 CFR 1320.16 (OMB Regulations on Controlling Paperwork Burdens on the Public). Board-approved collections of information are incorporated into the official OMB inventory of currently approved collections of information. Copies of the Paperwork Reduction Act Submission, supporting statements and approved collection of information instrument(s) are placed into OMB's public docket files. The Federal Reserve may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number.
Policy Letter 11-01, Performance of Inherently Governmental and Critical Functions
Document Number: 2012-3190
Type: Notice
Date: 2012-02-13
Agency: Management and Budget Office, Executive Office of the President, Office of Federal Procurement Policy
The Office of Federal Procurement Policy (OFPP) in the Office of Management and Budget (OMB) is making a correction to the Final Policy Letter ``Performance of Inherently Governmental and Critical Functions'' (76 FR 56227-56242, September 12, 2011) to clarify that the Policy Letter applies to both Civilian and Defense Executive Branch Departments and Agencies. The original publication of the policy letter was inadvertently addressed only to the Heads of The Civilian Executive Departments and Agencies. Also, OFPP has corrected the citation for additional guidance about conduct of Federally Funded Research and Development Centers (FFRDCs), because the original notice referenced an incorrect Part of the Federal Acquisition Regulation. The corrections below should be used in place of text previously published in the September 12, 2011 notice. All other information from the published Final Policy remains unchanged. The full text of the original notice is available at https://www.gpo.gov/fdsys/pkg/FR-2011-09-12/pdf/2011- 23165.pdf.
Revisions to the California State Implementation Plan, Joaquin Valley Unified Air Pollution Control District
Document Number: 2012-3172
Type: Rule
Date: 2012-02-13
Agency: Environmental Protection Agency
EPA is finalizing approval of revisions to the San Joaquin Valley Unified Air Pollution Control District (SJVUAPCD) portions of the California State Implementation Plan (SIP). These revisions were proposed in the Federal Register on October 6, 2011 and concern volatile organic compound (VOC) emissions from Motor Vehicle and Motor Equipment Coating Operations and Adhesives and Sealants. We are approving local rules that regulate these emission sources under the Clean Air Act as amended in 1990 (CAA or the Act).
Revisions to the California State Implementation Plan, California Air Resources Board-Consumer Products
Document Number: 2012-3169
Type: Rule
Date: 2012-02-13
Agency: Environmental Protection Agency
EPA is finalizing approval of revisions to the California Air Resources Board (CARB) portion of the California State Implementation Plan (SIP). These revisions were proposed in the Federal Register on October 6, 2011 and concern volatile organic compound (VOC) emissions from consumer products. We are approving a State rule that regulates these emission sources under the Clean Air Act as amended in 1990 (CAA or the Act).
Revision of Class D and Class E Airspace; Hawthorne, CA
Document Number: 2012-3149
Type: Rule
Date: 2012-02-13
Agency: Federal Aviation Administration, Department of Transportation
This action revises Class D and Class E airspace at Jack Northrop Field/Hawthorne Municipal Airport, Hawthorne, CA. Additional controlled airspace is needed to accommodate aircraft departing and arriving under Instrument Flight Rules (IFR) at the airport. Also, the airspace designations are revised to show a new city location. This action is a result of the FAA's biennial review, along with a study of the Jack Northrop Field/Hawthorne Municipal Airport airspace area that further enhances the safety and management of aircraft operations at the airport.
Public Notice for Waiver for Aeronautical Land-Use Assurance at Will Rogers World Airport, Oklahoma City, OK
Document Number: 2012-3146
Type: Notice
Date: 2012-02-13
Agency: Federal Aviation Administration, Department of Transportation
The Federal Aviation Administration (FAA) is considering a proposal to change a portion of the airport from aeronautical use to nonaeronautical use and to authorize the conversion of the airport property. The proposal consists of three parcels of land containing a total of approximately 127 acres located on the east side of the airport between South Portland Avenue and Interstate Highway 44. These parcels were originally acquired under the following grants: Airport Improvement Program (AIP) Nos. 3-40-0072-03 and 3-40-0072-07 in 1990; AIP No. 3-40-0072-23 in 1992; and AIP No. 3-40-0072-24 in 1993. The land comprising these parcels is outside the forecasted need for aviation development and, thus, is no longer needed for indirect or direct aeronautical use. The Airport wishes to develop this land for compatible commercial, nonaeronautical use. The income from the conversion of these parcels will benefit the aviation community by reinvestment in the airport. Approval does not constitute a commitment by the FAA to financially assist in the conversion of the subject airport property nor a determination of eligibility for grant-in-aid funding from the FAA. The disposition of proceeds from the conversion of the airport property will be in accordance with FAA's Policy and Procedures Concerning the Use of Airport Revenue, published in the Federal Register on February 16, 1999. In accordance with section 47107(h) of title 49, United States Code, this notice is required to be published in the Federal Register 30 days before modifying the land-use assurance that requires the property to be used for an aeronautical purpose.
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