Department of Health and Human Services April 13, 2007 – Federal Register Recent Federal Regulation Documents

Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: E7-7004
Type: Notice
Date: 2007-04-13
Agency: Office of the Secretary, Department of Health and Human Services
Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: E7-7003
Type: Notice
Date: 2007-04-13
Agency: Office of the Secretary, Department of Health and Human Services
Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: E7-7002
Type: Notice
Date: 2007-04-13
Agency: Office of the Secretary, Department of Health and Human Services
Agency Information Collection Activities: Submission For OMB Review; Comment Request
Document Number: E7-6992
Type: Notice
Date: 2007-04-13
Agency: Department of Health and Human Services, Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection: Comment Request
Document Number: E7-6991
Type: Notice
Date: 2007-04-13
Agency: Department of Health and Human Services, Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection; Comment Request
Document Number: E7-6990
Type: Notice
Date: 2007-04-13
Agency: Centers for Medicare & Medicaid Services, Department of Health and Human Services
Supplements and Other Changes to an Approved Application; Public Meeting; Reopening of Comment Period
Document Number: E7-6985
Type: Notice
Date: 2007-04-13
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is reopening until May 18, 2007, the comment period for a notice of public meeting that published in the Federal Register of January 5, 2007 (72 FR 574). In the notice, FDA announced a February 7, 2007, meeting to solicit input on issues that the agency should consider if it decides to propose revisions to its regulations regarding chemistry, manufacturing, and controls (CMC) supplements and other changes to approved marketing applications for human drugs. FDA is reopening the comment period in light of continued public interest in this topic.
National Vaccine Injury Compensation Program; List of Petitions Received
Document Number: E7-6984
Type: Notice
Date: 2007-04-13
Agency: Department of Health and Human Services, Health Resources and Services Administration
The Health Resources and Services Administration (HRSA) is publishing this notice of petitions received under the National Vaccine Injury Compensation Program (``the Program''), as required by Section 2112(b)(2) of the Public Health Service (PHS) Act, as amended. While the Secretary of Health and Human Services is named as the respondent in all proceedings brought by the filing of petitions for compensation under the Program, the United States Court of Federal Claims is charged by statute with responsibility for considering and acting upon the petitions.
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adoption of the Food and Drug Administration Food Code by Local, State, and Tribal Governments
Document Number: E7-6983
Type: Notice
Date: 2007-04-13
Agency: Food and Drug Administration, Department of Health and Human Services
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.
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