July 19, 2016 – Federal Register Recent Federal Regulation Documents

Results 101 - 108 of 108
Proposed Establishment of Temporary Restricted Areas R-2509E, R-2509W, and R-2509N; Twentynine Palms, CA; Withdrawal
Document Number: 2016-16922
Type: Proposed Rule
Date: 2016-07-19
Agency: Federal Aviation Administration, Department of Transportation
This action withdraws the NPRM published in the Federal Register of March 30, 2016, proposing to establish temporary restricted areas R-2509E, R-2509W, and R-2509N, Twentynine Palms, CA. The FAA has determined that withdrawal of that NPRM is warranted due to aeronautical impacts associated with the proposed action.
Board on Coastal Engineering Research
Document Number: 2016-16918
Type: Notice
Date: 2016-07-19
Agency: Department of Defense, Department of the Army, Corps of Engineers
The Department of the Army is publishing this notice to announce the following Federal advisory committee meeting of the Board on Coastal Engineering Research. This meeting is open to the public.
Prescription Drug User Fee Act; Public Meeting; Request for Comments
Document Number: 2016-16916
Type: Notice
Date: 2016-07-19
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA or Agency) is announcing a public meeting to discuss proposed recommendations for the reauthorization of the Prescription Drug User Fee Act (PDUFA) for fiscal years (FYs) 2018 through 2022. PDUFA authorizes FDA to collect fees and use them for the process for the review of human drug applications. The current legislative authority for PDUFA expires in September 2017. At that time, new legislation will be required for FDA to continue collecting prescription drug user fees in future fiscal years. Following discussions with the regulated industry and periodic consultations with public stakeholders, the Federal Food, Drug, and Cosmetic Act (the FD&C Act) directs FDA to publish the recommendations for the reauthorized program in the Federal Register, hold a meeting at which the public may present its views on such recommendations, and provide for a period of 30 days for the public to provide written comments on such recommendations. FDA will then consider such public views and comments and revise such recommendations as necessary.
Process Reform for Executive Branch Review of Certain FCC Applications and Petitions Involving Foreign Ownership
Document Number: 2016-16780
Type: Proposed Rule
Date: 2016-07-19
Agency: Federal Communications Commission, Agencies and Commissions
In this Notice of Proposed Rulemaking (NPRM), the Federal Communications Commission (Commission) proposes changes to our rules and procedures related to certain applications and petitions for declaratory ruling involving foreign ownership (together, ``applications''). The Commission refers certain applications to the relevant Executive Branch agencies for their input on any national security, law enforcement, foreign policy, and trade policy concerns that may arise from the foreign ownership interests held in the applicants and petitioners (together, ``applicants''). As part of our effort to reform the Commission's processes, we seek to improve the timeliness and transparency of this referral process. More specifically, our goals here are to identify ways in which both the Commission and the agencies might streamline and facilitate the process for obtaining information necessary for Executive Branch review and identify expected time frames, while ensuring that we continue to take Executive Branch concerns into consideration as part of our public interest review.
Expedited Approval of Alternative Test Procedures for the Analysis of Contaminants Under the Safe Drinking Water Act; Analysis and Sampling Procedures
Document Number: 2016-16516
Type: Rule
Date: 2016-07-19
Agency: Environmental Protection Agency
This action announces the U.S. Environmental Protection Agency's (EPA's) approval of alternative testing methods for use in measuring the levels of contaminants in drinking water and determining compliance with national primary drinking water regulations. The Safe Drinking Water Act authorizes EPA to approve the use of alternative testing methods through publication in the Federal Register. EPA is using this streamlined authority to make 16 additional methods available for analyzing drinking water samples. This expedited approach provides public water systems, laboratories, and primacy agencies with more timely access to new measurement techniques and greater flexibility in the selection of analytical methods, thereby reducing monitoring costs while maintaining public health protection.
Inversions and Related Transactions; Correction
Document Number: 2016-16470
Type: Rule
Date: 2016-07-19
Agency: Internal Revenue Service, Department of Treasury, Department of the Treasury
This document contains corrections to a correction document for final and temporary regulations (TD 9761) that was published in the Federal Register on June 23, 2016 (81 FR 40810).
Notice of Proposed Rulemaking
Document Number: 2016-16385
Type: Proposed Rule
Date: 2016-07-19
Agency: Federal Aviation Administration, Department of Transportation
This action proposes to modify the Class E airspace extending upward from 700 feet above the surface at Sonoma County Airport, Napa, CA, by removing an irregular shaped area located approximately 20 miles southwest of Napa County Airport. This airspace area is discontinuous from the airspace surrounding Napa County Airport and is not essential to instrument flight rules (IFR) operation at the airport. This proposal would also update the airport geographic coordinates. This action is necessary for the safety and management of instrument flight rules (IFR) operations at the airport, with the minimum amount of airspace restriction.
Agency Information Collection Request; 30-Day Public Comment Request, Grants.gov
Document Number: 2016-15982
Type: Notice
Date: 2016-07-19
Agency: Department of Health and Human Services