February 10, 2014 – Federal Register Recent Federal Regulation Documents

The Office of the General Counsel (OGC), Department of Veterans Affairs (VA), is announcing an opportunity for public comment on the modification of a collection of certain information by the agency. Under the Paperwork Reduction Act of 1995, Federal agencies are required to publish notice in the Federal Register concerning each modification of a collection of information, including each proposed revision of a currently approved collection, and allow 60 days for public comment in response to the notice. This notice solicits comments on the removal of the requirement that direct-pay fee agreements be filed with both the agency of original jurisdiction (AOJ) and OGC. Direct-pay fee agreements would only be filed with the AOJ.

Notice is hereby given, pursuant to CBP regulations, that Intertek USA Inc., has been approved to gauge petroleum and certain petroleum products for customs purposes for the next three years as of July 17, 2012.

Notice is hereby given, pursuant to CBP regulations, that Oiltest, Inc., has been approved to gauge petroleum and certain petroleum products and accredited to test petroleum and certain petroleum products for customs purposes for the next three years as of May 17, 2012.

Notice is hereby given, pursuant to CBP regulations, that American Cargo Assurance, has been approved to gauge petroleum and petroleum products for customs purposes for the next three years as of August 29, 2013.

The Department of Labor (DOL) is submitting the Employment and Training Administration (ETA) sponsored information collection request (ICR) titled, ``Benefits Timeliness and Quality Review System,'' to the Office of Management and Budget (OMB) for review and approval for continued use, without change, in accordance with the Paperwork Reduction Act of 1995 (PRA), 44 U.S.C. 3501 et seq.

The Consumer Product Safety Commission (CPSC or Commission) is announcing that a proposed collection of information regarding a survey of table saw users to determine the effectiveness of modular blade guards has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.

In accordance with Section 10(a) of the Federal Advisory Committee Act, Public Law 92-463, as amended (5 U.S.C. App.), notice is hereby given that a meeting is scheduled to be held for the Advisory Group on Prevention, Health Promotion, and Integrative and Public Health (the ``Advisory Group''). The meeting will be open to the public. Information about the Advisory Group and the agenda for this meeting can be obtained by accessing the following Web site: https:// www.surgeongeneral.gov/initiatives/prevention/advisorygrp/ind ex.html

In accordance with the Federal Land Policy and Management Act of 1976 and the Federal Advisory Committee Act of 1972, the U.S. Department of the Interior, Bureau of Land Management (BLM) Wyoming Resource Advisory Council (RAC) will meet as indicated below.

Breckenridge Ski Resort (BSR) has submitted a proposal to the White River National Forest (WRNF) to pursue approval of proposed projects included in its 2013 Master Development Plan (MDP) Addendum. The WRNF has accepted this proposal, and is preparing an Environmental Impact Statement (EIS) to analyze and disclose the potential environmental effects of implementing the projects. The Proposed Action is a range of projects designed to improve year-round recreation opportunities and better meet the changing needs and expectations of visitors to Breckenridge and the WRNF. The proposal hopes to better support a year-round economy in Breckenridge and Summit County by providing a diversity of attractions and outdoor activities that would attract visitors to the area. By providing a greater variety of activities and a longer season to visit BSR, the proposed educational and recreational opportunities would connect a more diverse group of visitors to our National Forest and the outdoors.

The Food and Drug Administration (FDA) is announcing the availability of the guidance entitled ``Annual Reports for Approved Premarket Approval Applications (PMA).'' The purpose of this guidance is to describe the information required to be included in an annual report for an approved PMA, additional information requirements that may be imposed by an approval order, and FDA's recommendations for the level of detail the applicant should provide in the annual report. It also identifies the steps FDA staff generally takes when reviewing annual reports, the resources available to assist staff in their reviews, and the regulatory actions they may recommend after reviewing annual reports.

The Department of Labor (DOL) is submitting the Occupational Safety and Health Administration (OSHA) sponsored information collection request (ICR) titled, ``Overhead and Gantry Cranes Standard,'' to the Office of Management and Budget (OMB) for review and approval for continued use, without change, in accordance with the Paperwork Reduction Act of 1995 (PRA), 44 U.S.C. 3501 et seq.

In accordance with the Paperwork Reduction Act of 1995, this notice announces the Animal and Plant Health Inspection Service's intention to request a revision to and extension of approval of an information collection associated with the interstate movement of animals affected with Johne's disease.

In accordance with the Paperwork Reduction Act of 1995, this notice announces the Animal and Plant Health Inspection Service's intention to request approval of a new information collection associated with the National Animal Health Laboratory Network qualification checklist for membership.

In accordance with the Paperwork Reduction Act of 1995, this notice announces the Animal and Plant Health Inspection Service's intention to request a revision to and extension of approval of an information collection associated with the regulations for blood and tissue collection at slaughtering and rendering establishments to enhance animal disease surveillance.

The Food and Drug Administration (FDA) is announcing a public conference entitled ``Serious Drug-Induced Liver Injury (DILI): Who Gets It? Who Doesn't? Why?'' This conference will be cosponsored with the Critical Path Institute (C-Path) and the Pharmaceutical Research and Manufacturers of America. Its purpose is to discuss, debate, and share views among stakeholders in the pharmaceutical industry, academia, health care providers, patient groups, and regulatory bodies on how best to detect and assess the severity, extent, and likelihood of drug causation of liver injury and dysfunction in people using drugs for any medical purpose.

The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.

The U.S. Nuclear Regulatory Commission (NRC) has recently submitted to OMB for review the following proposal for the collection of information under the provisions of the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). The NRC hereby informs potential respondents that an agency may not conduct or sponsor, and that a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. The NRC published a Federal Register notice with a 60-day comment period on this information collection on November 8, 2013 (78 FR 67204). 1. Type of submission, new, revision, or extension: Extension. 2. The title of the information collection: 10 CFR part 70, ``Domestic Licensing of Special Nuclear Material.'' 3. Current OMB approval number: 3150-0009. 4. The form number if applicable: Not applicable. 5. How often the collection is required: On occasion. Required reports are collected and evaluated on a continuing basis as events occur. Applications for new licenses and amendments may be submitted at any time. Generally, renewal applications are submitted every 10 years and for major fuel cycle facilities updates of the safety demonstration section are submitted every 2 years. Nuclear material control and accounting information is submitted in accordance with specified instructions. 6. Who will be required or asked to report: Applicants for and holders of specific NRC licenses to receive title to, own, acquire, deliver, receive, possess, use, or initially transfer special nuclear material. 7. An estimate of the number of annual responses: 1,620 responses. 8. The estimated number of annual respondents: 606. 9. An estimate of the total number of hours needed annually to complete the requirement or request: 89.240.6 hours (81,791.1 hours reporting + 7379.4 hours recordkeeping + 70.1 hours third party disclosure). 10. Abstract: Part 70 of Title 10 of the Code of Federal Regulations (10 CFR), establishes requirements for licenses to own, acquire, receive, possess, use, and transfer special nuclear material. The information in the applications, reports, and records is used by NRC to make licensing and other regulatory determinations concerning the use of special nuclear material. The public may examine and have copied for a fee publicly-available documents, including the final supporting statement, at the NRC's Public Document Room, Room O-1F21, One White Flint North, 11555 Rockville Pike, Rockville, Maryland 20852. The OMB clearance requests are available at the NRC's Web site: https://www.nrc.gov/public-involve/ doc-comment/omb/. The document will be available on the NRC's home page site for 60 days after the signature date of this notice. Comments and questions should be directed to the OMB reviewer listed below by March 12, 2014. Comments received after this date will be considered if it is practical to do so, but assurance of consideration cannot be given to comments received after this date.