Department of Health and Human Services November 26, 2010 – Federal Register Recent Federal Regulation Documents

Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
Document Number: 2010-29824
Type: Notice
Date: 2010-11-26
Agency: Food and Drug Administration, Department of Health and Human Services
Blood Products Advisory Committee; Notice of Meeting
Document Number: 2010-29818
Type: Notice
Date: 2010-11-26
Agency: Food and Drug Administration, Department of Health and Human Services
Submission for OMB Review; Comment Request
Document Number: 2010-29779
Type: Notice
Date: 2010-11-26
Agency: Department of Health and Human Services, Administration for Children and Families, Children and Families Administration
Los Alamos Historical Document Retrieval and Assessment (LAHDRA) Project
Document Number: 2010-29778
Type: Notice
Date: 2010-11-26
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Advisory Committee to the Director (ACD), Centers for Disease Control and Prevention (CDC)-Ethics Subcommittee (ES)
Document Number: 2010-29774
Type: Notice
Date: 2010-11-26
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2010-29752
Type: Notice
Date: 2010-11-26
Agency: Department of Health and Human Services, National Institutes of Health
National Institute on Deafness and Other Communication Disorders; Notice of Closed Meeting
Document Number: 2010-29751
Type: Notice
Date: 2010-11-26
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meeting
Document Number: 2010-29749
Type: Notice
Date: 2010-11-26
Agency: Department of Health and Human Services, National Institutes of Health
Office of the Director, National Institutes of Health; Notice of Meeting
Document Number: 2010-29748
Type: Notice
Date: 2010-11-26
Agency: Department of Health and Human Services, National Institutes of Health
Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications
Document Number: 2010-29731
Type: Notice
Date: 2010-11-26
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is publishing a list of premarket approval applications (PMAs) that have been approved. This list is intended to inform the public of the availability of safety and effectiveness summaries of approved PMAs through the Internet and the Agency's Division of Dockets Management.
Agency Information Collection Activities: Submission for OMB Review; Comment Request
Document Number: 2010-29718
Type: Notice
Date: 2010-11-26
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
New Animal Drugs; Change of Sponsor's Name and Address
Document Number: 2010-29693
Type: Rule
Date: 2010-11-26
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect a change of sponsor's name from Belcher Pharmaceuticals, Inc., to Belcher Pharmaceuticals, LLC. The sponsor's mailing address will also be changed.
Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Adoption of Food and Drug Administration Food Code by Local, State and Tribal Governments
Document Number: 2010-29688
Type: Notice
Date: 2010-11-26
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing that a collection of information entitled ``Adoption of FDA Food Code by Local, State and Tribal Governments'' has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
Agency Information Collection Activities; Proposed Collection; Comment Request; Current Good Manufacturing Practice Regulations for Type A Medicated Articles
Document Number: 2010-29687
Type: Notice
Date: 2010-11-26
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 recordkeeping requirements for manufacturers of type A medicated articles.
Medicare Program; Quality Improvement Organization (QIO) Contracts: Solicitation of Proposals From In-State QIOs-Idaho, Maine, South Carolina, and Vermont
Document Number: 2010-28817
Type: Notice
Date: 2010-11-26
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
This notice fulfills the Secretary's obligation under section 1153(i) of the Social Security Act (the Act) to provide at least 6 months' advance notice of the expiration dates of contracts with out- of-State Quality Improvement Organizations (QIOs) before renewing any of those QIOs' contracts. It also specifies the period of time in which in-State QIOs may submit a proposal for those contracts.
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