July 14, 2010 – Federal Register Recent Federal Regulation Documents

Results 101 - 122 of 122
Webinar About Advanced Defense Technologies RFP
Document Number: 2010-17071
Type: Notice
Date: 2010-07-14
Agency: Small Business Administration, Agencies and Commissions
The SBA is issuing this notice to announce the date of a webinar it is hosting to answer questions from potential Offerors about the Advanced Defense Technologies RFP. Please visit https://www.sba.gov/ clusters/ for more information. The RFP may be found on https://www.fedbizopps.gov.
Federal Register Meeting Notice; Webinar About Regional Innovation Clusters RFP
Document Number: 2010-17070
Type: Notice
Date: 2010-07-14
Agency: Small Business Administration, Agencies and Commissions
The SBA is issuing this notice to announce the date of a webinar it is hosting to answer questions from potential Offerors about the Regional Innovation Clusters RFP. For more information please go to https://www.sba.gov/clusters/. The RFP may be found on https:// www.fedbizopps.gov.
Town Hall Discussion With the Director of the Center for Devices and Radiological Health and Other Senior Center Management
Document Number: 2010-17068
Type: Notice
Date: 2010-07-14
Agency: Food and Drug Administration, Department of Health and Human Services
NASA Advisory Council; Exploration Committee; Meeting
Document Number: 2010-17063
Type: Notice
Date: 2010-07-14
Agency: National Aeronautics and Space Administration, Agencies and Commissions
In accordance with the Federal Advisory Committee Act, Public Law 92-463, as amended, the National Aeronautics and Space Administration announces a meeting of the Exploration Committee of the NASA Advisory Council.
Postal Rate Changes
Document Number: 2010-17056
Type: Notice
Date: 2010-07-14
Agency: Postal Regulatory Commission, Agencies and Commissions
Under a 2006 postal reform law, a new approach to implementing rate changes for market dominant postal products, which include First- Class Mail, was adopted. In general, the new approach envisions annual rate adjustments based on changes in a specified Consumer Price Index (CPI). However, the law includes a provision allowing rate changes in excess of CPI under extraordinary or exceptional circumstances, contingent on a Commission determination on certain considerations. The Postal Service is invoking this provision for the first time and, in a filing with the Commission, is seeking an overall percentage increase of about 5.6 percent for market dominant products beginning January 2, 2011. It is also seeking some classification changes. This document provides the public with notice of the Postal Service's filing, a brief description of the contents, a discussion of the Commission's role and responsibilities, and an outline of related procedural steps.
International Conference on Harmonisation; Draft Guidance on Q4B Evaluation and Recommendation of Pharmacopoeial Texts for Use in the International Conference on Harmonisation Regions; Annex 13 on Bulk Density and Tapped Density of Powders General Chapter; Availability
Document Number: 2010-17055
Type: Notice
Date: 2010-07-14
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 entitled ``Q4B Evaluation and Recommendation of Pharmacopoeial Texts for Use in the ICH Regions; Annex 13: Bulk Density and Tapped Density of Powders General Chapter.'' The draft guidance was prepared under the auspices of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The draft guidance provides the results of the ICH Q4B evaluation of the Bulk Density and Tapped Density of Powders General Chapter harmonized text from each of the three pharmacopoeias (United States, European, and Japanese) represented by the Pharmacopoeial Discussion Group (PDG). The draft guidance conveys recognition of the three pharmacopoeial methods by the three ICH regulatory regions and provides specific information regarding the recognition. The draft guidance is intended to recognize the interchangeability between the local regional pharmacopoeias, thus avoiding redundant testing in favor of a common testing strategy in each regulatory region. This draft guidance is the thirteenth annex to the core Q4B guidance, which was made available in the Federal Register of February 21, 2008 (73 FR 9575).
Agency Information Collection Activities; Proposed Collection; Comment Request; Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements
Document Number: 2010-17054
Type: Notice
Date: 2010-07-14
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information collection provisions of FDA's regulations regarding current good manufacturing practice (CGMP) for dietary supplements.
Hexythiazox; Pesticide Tolerances
Document Number: 2010-17034
Type: Rule
Date: 2010-07-14
Agency: Environmental Protection Agency
This regulation revises tolerances for combined residues of hexythiazox in or on stone fruit. Gowan Company requested these tolerances under the Federal Food, Drug, and Cosmetic Act (FFDCA).
Cyazofamid; Pesticide Tolerances
Document Number: 2010-17025
Type: Rule
Date: 2010-07-14
Agency: Environmental Protection Agency
This regulation establishes tolerances for residues of cyazofamid in or on Brassica, head and stem, subgroup 5A; Brassica, leafy greens, subgroup 5B; turnip, greens; spinach; and hop, dried cones. Interregional Research Project Number 4 (IR-4) requested these tolerances under the Federal Food, Drug, and Cosmetic Act (FFDCA).
Clofencet; Cancellation Order for Certain Pesticide Registrations
Document Number: 2010-17020
Type: Notice
Date: 2010-07-14
Agency: Environmental Protection Agency
This notice announces EPA's order for the cancellations, voluntarily requested by the registrant and accepted by the Agency, of products containing clofencet, pursuant to section 6(f)(1) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), as amended. This cancellation order follows an April 28, 2010 Federal Register Notice of Receipt of Request from the registrant Monsanto Company to voluntarily cancel all these product registrations. These are the last products containing this pesticide registered for use in the United States. In the April 28, 2010 notice, EPA indicated that it would issue an order implementing the cancellations, unless the Agency received substantive comments within the 30-day comment period that would merit its further review of this request, or unless the registrant withdrew their request. The Agency did not receive any comments on the notice. Further, the registrant did not withdraw their request. Accordingly, EPA hereby issues in this notice a cancellation order granting the requested cancellations. Any distribution, sale, or use of the products subject to this cancellation order is permitted only in accordance with the terms of this order, including any existing stocks provisions.
Rotenone; Cancellation Order for Amendments to Terminate Uses
Document Number: 2010-17015
Type: Notice
Date: 2010-07-14
Agency: Environmental Protection Agency
This notice announces EPA's order for amendments to terminate uses, voluntarily requested by the registrants and accepted by the Agency, of products containing rotenone, pursuant to section 6(f)(1) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), as amended. This cancellation order follows a June 7, 2006 Federal Register Notice of Receipt of Requests from the registrants listed in Table 2 of Unit II. to voluntarily amend to terminate uses of these product registrations. These are not the last products containing this pesticide registered for use in the United States. In the June 7, 2006 notice, EPA indicated that it would issue an order implementing the amendments to terminate uses, unless the Agency received substantive comments within the 30 day comment period that would merit its further review of these requests, or unless the registrants withdrew their requests. The Agency received one comment on the notice but it did not merit further review of the requests. Further, the registrants did not withdraw their requests. Accordingly, EPA hereby issues in this notice a cancellation order granting the requested amendments to terminate uses. Any distribution, sale, or use of the products subject to this cancellation order is permitted only in accordance with the terms of this order, including any existing stocks provisions.
Establishment of Class E Airspace; Kemmerer, WY
Document Number: 2010-17006
Type: Rule
Date: 2010-07-14
Agency: Federal Aviation Administration, Department of Transportation
This action will establish Class E airspace at Kemmerer, WY to accommodate aircraft using a new Area Navigation (RNAV) Global Positioning System (GPS) Standard Instrument Approach Procedures (SIAPs) at Kemmerer Municipal Airport. This will improve the safety and management of Instrument Flight Rules (IFR) operations at the airport.
Data Collection Available for Public Comments and Recommendations
Document Number: 2010-16935
Type: Notice
Date: 2010-07-14
Agency: Small Business Administration, Agencies and Commissions
In accordance with the Paperwork Reduction Act of 1995, this notice announces the Small Business Administration's intentions to request approval on a new and/or currently approved information collection.
Methyl Soyate; Receipt of Application for Emergency Exemption, Solicitation of Public Comment
Document Number: 2010-16923
Type: Notice
Date: 2010-07-14
Agency: Environmental Protection Agency
EPA has received a specific exemption request from the Wyoming Department of Agriculture to use the pesticide methyl soyate (BIO-LARV) (CAS Reg. No. 67762-38-3) to treat aquatic vegetation to control mosquito larvae. The applicant proposes the use of a new chemical which has not been registered by EPA. EPA is soliciting public comment before making the decision whether or not to grant the exemption.
Modifications to the HIPAA Privacy, Security, and Enforcement Rules Under the Health Information Technology for Economic and Clinical Health Act
Document Number: 2010-16718
Type: Proposed Rule
Date: 2010-07-14
Agency: Office of the Secretary, Department of Health and Human Services
The Department of Health and Human Services (HHS or ``the Department'') is issuing this notice of proposed rulemaking to modify the Standards for Privacy of Individually Identifiable Health Information (Privacy Rule), the Security Standards for the Protection of Electronic Protected Health Information (Security Rule), and the rules pertaining to Compliance and Investigations, Imposition of Civil Money Penalties, and Procedures for Hearings (Enforcement Rule) issued under the Health Insurance Portability and Accountability Act of 1996 (HIPAA). The purpose of these modifications is to implement recent statutory amendments under the Health Information Technology for Economic and Clinical Health Act (``the HITECH Act'' or ``the Act''), to strengthen the privacy and security protection of health information, and to improve the workability and effectiveness of these HIPAA Rules.
Political Contributions by Certain Investment Advisers
Document Number: 2010-16559
Type: Rule
Date: 2010-07-14
Agency: Securities and Exchange Commission, Agencies and Commissions
The Securities and Exchange Commission is adopting a new rule under the Investment Advisers Act of 1940 that prohibits an investment adviser from providing advisory services for compensation to a government client for two years after the adviser or certain of its executives or employees make a contribution to certain elected officials or candidates. The new rule also prohibits an adviser from providing or agreeing to provide, directly or indirectly, payment to any third party for a solicitation of advisory business from any government entity on behalf of such adviser, unless such third parties are registered broker-dealers or registered investment advisers, in each case themselves subject to pay to play restrictions. Additionally, the new rule prevents an adviser from soliciting from others, or coordinating, contributions to certain elected officials or candidates or payments to political parties where the adviser is providing or seeking government business. The Commission also is adopting rule amendments that require a registered adviser to maintain certain records of the political contributions made by the adviser or certain of its executives or employees. The new rule and rule amendments
National Primary Drinking Water Regulations: Revisions to the Total Coliform Rule
Document Number: 2010-15205
Type: Proposed Rule
Date: 2010-07-14
Agency: Environmental Protection Agency
The Environmental Protection Agency (EPA or the Agency) is proposing revisions to the 1989 Total Coliform Rule. The proposed Revised Total Coliform Rule offers a meaningful opportunity for greater public health protection beyond the current Total Coliform Rule. The proposed revisions require systems that have an indication of coliform contamination in the distribution system to assess the problem and take corrective action that may reduce cases of illnesses and deaths due to potential fecal contamination and waterborne pathogen exposure. This proposal also updates provisions in other rules that reference analytical methods and other requirements in the current TCR (e.g., Public Notification and Ground Water Rules). These proposed revisions are in accordance with the Safe Drinking Water Act as amended, which requires EPA to review and revise, as appropriate, each national primary drinking water regulation promulgated under the Safe Drinking Water Act not less often than every six years. As with the current Total Coliform Rule, the proposed Revised Total Coliform Rule applies to all public water systems.
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