Department of Health and Human Services January 8, 2010 – Federal Register Recent Federal Regulation Documents

Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: E9-31301
Type: Notice
Date: 2010-01-08
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
Agency Information Collection Activities: Submission for OMB Review; Comment Request
Document Number: E9-31299
Type: Notice
Date: 2010-01-08
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2010-99
Type: Notice
Date: 2010-01-08
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2010-98
Type: Notice
Date: 2010-01-08
Agency: Department of Health and Human Services, National Institutes of Health
Eunice Kennedy Shriver National Institute of Child Health and Human Development; Notice of Meeting
Document Number: 2010-97
Type: Notice
Date: 2010-01-08
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Dental & Craniofacial Research; Notice of Closed Meeting
Document Number: 2010-96
Type: Notice
Date: 2010-01-08
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Allergy and Infectious Diseases; Notice of Meeting
Document Number: 2010-95
Type: Notice
Date: 2010-01-08
Agency: Department of Health and Human Services, National Institutes of Health
Draft Guidance for Industry on Planning for the Effects of High Absenteeism to Ensure Availability of Medically Necessary Drug Products; Availability
Document Number: 2010-87
Type: Notice
Date: 2010-01-08
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The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled ``Planning for the Effects of High Absenteeism to Ensure Availability of Medically Necessary Drug Products.'' The draft guidance encourages manufacturers of medically necessary drug products (MNPs) and components to develop contingency production plans in the event of an emergency that results in high absenteeism at one or more production facilities. The purpose of the draft guidance is to provide to industry considerations for developing such emergency plans, as well as to discuss the Center for Drug Evaluation and Research's (CDER's) intended approach to assist in avoiding drug product shortages that may have a negative impact on the national public health during such emergencies.
Certain Other Dosage Form New Animal Drugs; Sevoflurane
Document Number: 2010-47
Type: Rule
Date: 2010-01-08
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 approval of an abbreviated new animal drug application (ANADA) filed by Halocarbon Products Corp. The ANADA provides for the use of sevoflurane inhalant anesthetic in dogs.
Board of Scientific Counselors, National Center for Injury Prevention and Control, (BSC, NCIPC)
Document Number: 2010-22
Type: Notice
Date: 2010-01-08
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services, Alcohol, Tobacco, Firearms, and Explosives Bureau, Department of Justice
President's Advisory Council for Faith-based and Neighborhood Partnerships
Document Number: 2010-145
Type: Notice
Date: 2010-01-08
Agency: Department of Health and Human Services
Clinical Laboratory Improvement Advisory Committee (CLIAC)
Document Number: 2010-100
Type: Notice
Date: 2010-01-08
Agency: Centers for Disease Control and Prevention, Department of Health and Human Services, Alcohol, Tobacco, Firearms, and Explosives Bureau, Department of Justice
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