Department of Health and Human Services August 16, 2005 – Federal Register Recent Federal Regulation Documents
Results 1 - 25 of 25
Notice of Hearing: Reconsideration of Disapproval of Maryland State Plan Amendment (05-06)
This notice announces an administrative hearing to be held on September 15, 2005, at 12 noon, in the Virginia Room 229, 150 S. Independence Mall, West, Suite 216, Philadelphia, Pennsylvania 19106, to reconsider our decision to disapprove Maryland's State Plan Amendment (SPA) 05-06.
Vision 2006-A Conversation With the American Public; Notice of Public Meetings on Specific Food and Drug Administration Issues; Request for Comments
The Food and Drug Administration (FDA) is announcing a series of public meetings entitled ``Vision 2006A Conversation With the American Public,'' in three cities. This forum will be an open format in which consumers can interact directly with the agency's leadership to discuss what is on the public's mind. It will also be an opportunity for the agency to update the public on current agency programs, engage the public in discussion, and obtain consumer input on specific issues. We may use the public input we receive to evaluate and to propose modifications, if necessary, to our programs and activities.
Irradiation in the Production, Processing, and Handling of Food
The Food and Drug Administration (FDA) is amending the food additive regulations to provide for the safe use of ionizing radiation for control of Vibrio species and other foodborne pathogens in fresh or frozen molluscan shellfish (e.g., oysters, mussels, clams, etc.). This action is in response to a petition filed by the National Fisheries Institute and the Louisiana Department of Agriculture and Forestry.
Epidemiologic Study of Inflammatory Bowel Disease; Notice of Intent To Fund Single Eligibility Award
Turtles Intrastate and Interstate Requirements
The Food and Drug Administration (FDA) is amending its regulation regarding the intrastate and interstate distribution of turtles to reflect a change in responsibility for administering the provisions of the regulations from FDA's Center for Food Safety and Applied Nutrition (CFSAN) to FDA's Center for Veterinary Medicine (CVM). FDA is taking this action to enable the agency to more effectively administer the provisions of this regulation.
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; MedWatch: Food and Drug Administration Medical Products Reporting Program
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
This site is protected by reCAPTCHA and the Google
Privacy Policy and
Terms of Service apply.
