Department of Health and Human Services September 20, 2011 – Federal Register Recent Federal Regulation Documents

Center for Scientific Review Amended Notice of Meeting
Document Number: 2011-24144
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, National Institutes of Health
Eunice Kennedy Shriver National Institute of Child Health & Human Development Notice of Closed Meeting
Document Number: 2011-24136
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Dental and Craniofacial Research; Notice of Closed Meetings
Document Number: 2011-24135
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2011-24134
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, National Institutes of Health
National Heart, Lung, and Blood Institute Notice of Closed Meetings
Document Number: 2011-24133
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Mental Health Notice of Closed Meetings
Document Number: 2011-24132
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review Notice of Closed Meetings
Document Number: 2011-24130
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, National Institutes of Health
National Advisory Council on Migrant Health; Notice of Meeting
Document Number: 2011-24127
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB Review; Comment Request
Document Number: 2011-24121
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services, Health Resources and Services Administration
Animal Generic Drug User Fee Act; Public Meeting; Request for Comments
Document Number: 2011-24083
Type: Notice
Date: 2011-09-20
Agency: Food and Drug Administration, Department of Health and Human Services
Animal Drug User Fee Act; Public Meeting; Request for Comments
Document Number: 2011-24082
Type: Notice
Date: 2011-09-20
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing a public meeting on the Animal Drug User Fee Act (ADUFA). FDA invites public comment on the ADUFA program and suggestions regarding the features FDA should propose for the next ADUFA program. Date and Time: The meeting will be held on November 7, 2011, from 9 a.m. to 12 noon. Location: The meeting will be held at the Food and Drug Administration, 7519 Standish Pl., 3d floor, Rm. A, Rockville, MD 20855. If you require special accommodations, please contact Patricia Arnwine (see Contact Person) at least 7 days before the meeting. Contact Person: Donal Parks, Food and Drug Administration, Center for Veterinary Medicine, 7519 Standish Pl., Rockville, MD 20855, 240- 276-8688, FAX: 240-276-9744, Donal.Parks@fda.hhs.gov, or Patricia Arnwine, Food and Drug Administration, Center for Veterinary Medicine, 7519 Standish Pl., Rockville, MD 20855, 240-276-9724, FAX: 240-276- 9744, Patricia.Arnwine@fda.hhs.gov. Comments: Regardless of attendance at the meeting, interested persons may submit either electronic or written comments regarding this document. Submit electronic comments to https://www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA- 305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Identify comments with the docket number found in brackets in the heading of this document. Comments received by October 26, 2011, will be taken into consideration before the public meeting. Transcripts: Transcripts of the meeting will be available for review at the Division of Dockets Management and on the Internet at https://www.fda.gov/ForIndustry/UserFees/AnimalDrugUserFeeActA DUFA/ ucm042891.htm approximately 30 days after the meeting.
Performance Review Board Members
Document Number: 2011-24039
Type: Notice
Date: 2011-09-20
Agency: Department of Health and Human Services
Magnetic Resonance Imaging Safety; Public Workshop
Document Number: 2011-24030
Type: Notice
Date: 2011-09-20
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing a public workshop entitled: ``Magnetic Resonance Imaging (MRI) Safety Public Workshop.'' The purpose of the public workshop is to discuss factors affecting the safe use of magnetic resonance imaging (MRI) and approaches to mitigate risks. The overall goal is to discuss strategies to minimize patient and staff risk in the MRI environment.
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