Department of Health and Human Services April 9, 2015 – Federal Register Recent Federal Regulation Documents

Food and Drug Administration Science Forum 2015; Public Workshop
Document Number: 2015-08156
Type: Notice
Date: 2015-04-09
Agency: Food and Drug Administration, Department of Health and Human Services
Proposed Collection; 60-Day Comment Request: United States and Global Human Influenza Surveillance in at-Risk Settings
Document Number: 2015-08149
Type: Notice
Date: 2015-04-09
Agency: Department of Health and Human Services, National Institutes of Health
In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. Written comments and/or suggestions from the public and affected agencies are invited on one or more of the following points: (1) Whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) The accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) Ways to enhance the quality, utility, and clarity of the information to be collected; and (4) Ways to minimize the burden of the collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology.
Agency Forms Undergoing Paperwork Reduction Act Review; Withdrawal
Document Number: 2015-08139
Type: Notice
Date: 2015-04-09
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Due to an information collection request oversight, the Centers for Disease Control and Prevention (CDC) requests immediate publication withdrawal of the 30-Day Federal Register Notice (FRN) entitled ``Agency Forms Undergoing Paperwork Reduction Act Review'' concerning the Public Health Associate Program (PHAP) Alumni Assessment.
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2015-08133
Type: Notice
Date: 2015-04-09
Agency: Department of Health and Human Services, National Institutes of Health
National Institute on Aging; Notice of Closed Meetings
Document Number: 2015-08132
Type: Notice
Date: 2015-04-09
Agency: Department of Health and Human Services, National Institutes of Health
National Cancer Institute; Notice of Closed Meetings
Document Number: 2015-08131
Type: Notice
Date: 2015-04-09
Agency: Department of Health and Human Services
National Cancer Institute Amended; Notice of Meeting
Document Number: 2015-08130
Type: Notice
Date: 2015-04-09
Agency: Department of Health and Human Services, National Institutes of Health
National Eye Institute; Notice of Meeting
Document Number: 2015-08129
Type: Notice
Date: 2015-04-09
Agency: Department of Health and Human Services, National Institutes of Health
Amendments to Registration of Food Facilities
Document Number: 2015-08018
Type: Proposed Rule
Date: 2015-04-09
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA or we) is proposing to amend its regulation for registration of food facilities that requires domestic and foreign facilities that manufacture/process, pack, or hold food for human or animal consumption in the United States to register with FDA. This proposed rule would amend and update FDA's registration regulations and is part of our implementation of the FDA Food Safety Modernization Act (FSMA), which added new provisions for the registration of food facilities. Moreover, a number of provisions in FSMA apply only to facilities required to register, including hazard analysis and risk-based preventive controls and mandatory recall authority. The proposed amendments will further enhance FDA's capabilities with respect to responding to food safety issues, and in addition, provide FDA with information that we can use to focus and better utilize our limited inspection resources.
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