Department of Health and Human Services March 1, 2010 – Federal Register Recent Federal Regulation Documents

Agency Information Collection Activities: Submission for OMB Review; Comment Request
Document Number: 2010-4186
Type: Notice
Date: 2010-03-01
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
National Cancer Institute; Amended Notice of Meeting
Document Number: 2010-4184
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Diabetes and Digestive and Kidney Diseases; Notice of Closed Meetings
Document Number: 2010-4183
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Diabetes and Digestive and Kidney Diseases; Notice of Closed Meeting
Document Number: 2010-4181
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services, National Institutes of Health
Office of Dietary Supplements (ODS) 2010-2014 Strategic Plan
Document Number: 2010-4180
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services, National Institutes of Health
The Office of Dietary Supplements (ODS) at the National Institutes of Health (NIH) has completed a strategic planning process resulting in the development of the ODS Strategic Plan for 2010-2014, entitled Strengthening Knowledge and Understanding of Dietary Supplements. The strategic plan is available in pdf format on the ODS Web site: https://ods.od.nih.gov/pubs/strategicplan/StrategicPlan2010- 2014.pdf.
Center for Scientific Review; Notice of Closed Meeting
Document Number: 2010-4178
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services, National Institutes of Health
Agency Forms Undergoing Paperwork Reduction Act Review
Document Number: 2010-4177
Type: Notice
Date: 2010-03-01
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Proposed Data Collections Submitted for Public Comment and Recommendations
Document Number: 2010-4164
Type: Notice
Date: 2010-03-01
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Determination of Regulatory Review Period for Purposes of Patent Extension; FIRMAGON
Document Number: 2010-4159
Type: Notice
Date: 2010-03-01
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) has determined the regulatory review period for FIRMAGON and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of an application to the Director of Patents and Trademarks, Department of Commerce, for the extension of a patent which claims that human drug product.
Meeting of the Advisory Committee on Minority Health
Document Number: 2010-4123
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services
As stipulated by the Federal Advisory Committee Act, the Department of Health and Human Services (DHHS) is hereby giving notice that the Advisory Committee on Minority Health (ACMH) will hold a meeting. This meeting is open to the public. Preregistration is required for both public attendance and comment. Any individual who wishes to attend the meeting and/or participate in the public comment session should e-mail acmh@osophs.dhhs.gov.
Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: 2010-4117
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services, Substance Abuse and Mental Health Services Administration
Administration on Aging Agency Information Collection Activities; Proposed Collection; Comment Request; Extension of a Currently Approved Information Collection; Program Announcement and Grant Application Instructions Template for the Older Americans Act Title IV Discretionary Grant Program
Document Number: 2010-4112
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services
The Administration on Aging (AoA) 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 requirements relating to the standard Program Announcement and Grant Application Instructions template for Older Americans Act Title IV Discretionary Grant Program.
Measuring Progress on Food Safety: Current Status and Future Directions; Public Workshop
Document Number: 2010-4110
Type: Notice
Date: 2010-03-01
Agency: Food and Drug Administration, Department of Health and Human Services
Draft Guidance for Industry on Non-Inferiority Clinical Trials; Availability
Document Number: 2010-4109
Type: Notice
Date: 2010-03-01
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 for industry entitled ``Non- Inferiority Clinical Trials.'' This draft guidance provides sponsors and review staff in the Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) with the agency's interpretation of the underlying principles involved in the use of non-inferiority (NI) study designs to provide evidence of the effectiveness of a drug or therapeutic biologic product. The draft guidance offers advice on when NI studies can be interpretable, how to choose the NI margin, and how to analyze the results.
Agency Information Collection Activities; Proposed Collection; Comment Request; Pretesting of Tobacco Communications
Document Number: 2010-4098
Type: Notice
Date: 2010-03-01
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, and to allow 60 days for public comment in response to the notice. This notice solicits comments on pretesting of tobacco communications.
Agency Information Collection Activities; Proposed Collection; Comment Request; Human Tissue Intended for Transplantation
Document Number: 2010-4066
Type: Notice
Date: 2010-03-01
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 requirements relating to FDA regulations for human tissue intended for transplantation.
Current List of Laboratories Which Meet Minimum Standards To Engage in Urine Drug Testing for Federal Agencies
Document Number: 2010-3973
Type: Notice
Date: 2010-03-01
Agency: Department of Health and Human Services, Substance Abuse and Mental Health Services Administration
The Department of Health and Human Services (HHS) notifies Federal agencies of the laboratories currently certified to meet the standards of Subpart C of the Mandatory Guidelines for Federal Workplace Drug Testing Programs (Mandatory Guidelines). The Mandatory Guidelines were first published in the Federal Register on April 11, 1988 (53 FR 11970), and subsequently revised in the Federal Register on June 9, 1994 (59 FR 29908), on September 30, 1997 (62 FR 51118), and on April 13, 2004 (69 FR 19644).
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.