Department of Health and Human Services May 15, 2009 – Federal Register Recent Federal Regulation Documents

National Advisory Committee on Rural Health and Human Services; Notice of Meeting
Document Number: E9-11441
Type: Notice
Date: 2009-05-15
Agency: Department of Health and Human Services, Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB Review; Comment Request
Document Number: E9-11424
Type: Notice
Date: 2009-05-15
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: E9-11422
Type: Notice
Date: 2009-05-15
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
Agency Forms Undergoing Paperwork Act Review
Document Number: E9-11379
Type: Notice
Date: 2009-05-15
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services
Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: E9-11377
Type: Notice
Date: 2009-05-15
Agency: Department of Health and Human Services, Substance Abuse and Mental Health Services Administration
Current List of Laboratories Which Meet Minimum Standards To Engage in Urine Drug Testing for Federal Agencies
Document Number: E9-11374
Type: Notice
Date: 2009-05-15
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).
New Animal Drugs; Gentamicin and Betamethasone Spray
Document Number: E9-11368
Type: Rule
Date: 2009-05-15
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 the original approval of an abbreviated new animal drug application (ANADA) filed by American Pharmaceuticals and Cosmetics, Inc. The ANADA provides for the veterinary prescription use of gentamicin sulfate and betamethasone valerate topical spray in dogs.
Proposed Information Collection Activity; Comment Request
Document Number: E9-11364
Type: Notice
Date: 2009-05-15
Agency: Department of Health and Human Services, Administration for Children and Families, Children and Families Administration
Small Entity Compliance Guide: Health Claims; Calcium and Osteoporosis, and Calcium, Vitamin D, and Osteoporosis; Availability
Document Number: E9-11320
Type: Notice
Date: 2009-05-15
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing the availability of a guidance for industry entitled ``Food Labeling: Health Claims; Calcium and Osteoporosis, and Calcium, Vitamin D, and OsteoporosisSmall Entity Compliance Guide.'' The small entity compliance guide (SECG) is being issued for a final rule published in the Federal Register of September 29, 2008, as corrected on November 12, 2008, and it is intended to set forth in plain language the legal requirements of the regulation and to help small businesses understand the regulation.
Request for Nominations for Voting Consumer Representative Members on Public Advisory Committees
Document Number: E9-11319
Type: Notice
Date: 2009-05-15
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is requesting nominations for voting consumer representatives to serve on the Food Advisory Committee. This advisory committee is under the purview of the Center for Food Safety and Applied Nutrition (CFSAN).
Pediatric Advisory Committee; Notice of Meeting
Document Number: E9-11317
Type: Notice
Date: 2009-05-15
Agency: Food and Drug Administration, Department of Health and Human Services
Hospital Preparedness Program (HPP)
Document Number: E9-11307
Type: Notice
Date: 2009-05-15
Agency: Office of the Secretary, Department of Health and Human Services
This notice sets forth the Secretary's decision to require Hospital Preparedness Program [HPP] cooperative agreement recipients to contribute non-Federal matching funds starting with the FY 2009 funding cycle and each year thereafter. The amount of the cost sharing requirement in FY 2009 will be five percent of the award amount and in FY 2010 and each year thereafter the amount of match will be ten percent of the award amount.
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