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3326. Agency Information Collection Activities: Submission for OMB Review; Comment Request

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

Periodically, the Health Resources and Services Administration (HRSA) publishes abstracts of information collection requests under review by the Office of Management and Budget (OMB), in compliance with the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request a copy of the clearance requests submitted to OMB for review, call the

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Health Resources and Services Administration

3327. National Advisory Council on Migrant Health; Notice of Meeting

NOTICES: Migrant Health National Advisory Council,

In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92463), notice is hereby given of the following meeting:

Name: National Advisory Council on Migrant Health.

Dates and Times: February 5, 2007, 8:30 a.m. to 5 p.m.;February 6, 2007, 8:30 a.m. to 5 p.m.

Place: 5600 Fishers Lane, Potomac Room, 3rd Floor,

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Health Resources and Services Administration

3328. Conventional Foods Being Marketed as ``Functional Foods''; Extension of Comment Period

PROPOSED RULES: Food labeling—; Conventional foods being marketed as functional foods; hearing,

The Food and Drug Administration (FDA) is extending to March 5, 2007, the comment period for the notice of public hearing that appeared in the Federal Register of October 25, 2006 (71 FR 62400). In the notice of public hearing, FDA requested comments on how the agency should regulate conventional foods marketed as ``functional foods'' under its
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3329. Agency Information Collection Activities; Proposed Collection; Comment Request; Threshold of Regulation for

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3330. International Conference on Harmonisation; Draft Guidance on E15 Terminology in Pharmacogenomics; Availability

NOTICES: International Conference on Harmonisation—; Pharmacogenomics; E15 terminology,

The Food and Drug Administration (FDA) is announcing the availability of a draft guidance entitled ``E15 Terminology in Pharmacogenomics.'' The draft guidance was prepared under the auspices of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The draft guidance
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3331. Notice of Meeting of the Advisory Committee on Minority Health

NOTICES: Minority Health Advisory Committee,

As stipulated by the Federal Advisory Committee Act, the Department of Health and Human Services (DHHS) is hereby giving notice that the Advisory Committee on Minority Health (ACMH) will hold a meeting. This meeting is open to the public. Preregistration is required for both public attendance and comment. Any individual who wishes to attend the
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Health and Human Services Department

3332. Agency Information Collection Activities: Submission for OMB Review; Comment Request

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

Periodically, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish a summary of information collection requests under OMB review, in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these documents, call the SAMHSA Reports Clearance Officer on (240) 2761243.

Proposed

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Substance Abuse and Mental Health Services Administration

3333. Submission for OMB Review; Comment Request

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

Title: Evaluation of the Community Healthy Marriage Initiative.

OMB No.: No collection.

Description: The administration for Children and Families, United States Department of Health and Human Services, is conducting a demonstration and evaluation called Community Healthy Marriage Initiative (CHMI). Demonstration programs will be funded

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Children and Families Administration

3334. Proposed Information Collection Activity; Comment Request

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

Proposed Projects:

Title: Evaluation of the Refugee Social Service (RSS) and Targeted Assistant Formula Grant (TAG) Programs: Data Collection.

OMB No.: 09700296.

Description: The Office of Refugee Resettlement (ORR) within the U.S. Department of Health and Human Services (HHS) funds the Refugee Social Services (RSS) and Targeted

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Children and Families Administration

3335. Submission for OMB Review; Comment Request

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

Title: DHHS/ACF/ASPE/DOL Enhanced Services for the HardtoEmploy Demonstration and Evaluation: Rhode Island 15Month Survey Amendment.

OMB No. 09700276.

Description: The Enhanced Services for the HardtoEmploy Demonstration and Evaluation Project (HtE) seeks to learn what works in this area to date and is explicitly designed to build on

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Children and Families Administration

3336. New Animal Drugs For Use in Animal Feeds; Monensin

RULES: Monensin,

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Elanco Animal Health. The supplemental NADA revises the concentration of monensin in Type C medicated feeds used for improved feed efficiency, and for the prevention and control of
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3337. Agency Forms Undergoing Paperwork Reduction Act Review

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 6395960 or send an email

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention

3338. Agency Forms Undergoing Paperwork Reduction Act Review

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 6395960 or send an email

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention

3339. National Center for Environmental Health/Agency for Toxic Substances and Disease Registry

NOTICES: National Center for Environmental Health/Agency for Toxic Substances and Disease Registry—; Scientific Counselors Board,

The Health Department Subcommittee of the Board of Scientific Counselors (BSC), Centers for Disease Control and Prevention (CDC), National Center for Environmental Health (NCEH)/Agency for Toxic Substances and Disease Registry (ATSDR): Teleconference Meeting.

In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L.

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Disease Control and Prevention

3340. Agency Information Collection Activities: Proposed Collection; Comment Request

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Medicare & Medicaid Services

3341. Agency Information Collection Activities: Submission for OMB Review; Comment Request

NOTICES: Agency information collection activities; proposals, submissions, and approvals,

DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Medicare & Medicaid Services

3342. Medicare Program; Changes to the Hospital Inpatient Prospective Payment Systems and Fiscal Year 2007 Rates; Final

NOTICES: Hospital inpatient prospective payment systems and 2007 FY rates; correction,

This document corrects wage index and technical errors that appeared in the notice published in the Federal Register on October 11, 2006 entitled ``Medicare Program; Hospital Inpatient Prospective Payment Systems and Fiscal Year 2007 Rates.
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Centers for Medicare & Medicaid Services

3343. Food Labeling: Health Claims; Calcium and Osteoporosis, and Calcium, Vitamin D, and Osteoporosis

PROPOSED RULES: Food labeling—; Calcium, vitamin D, and osteoporosis; nutrient content claims,

The Food and Drug Administration (FDA) is proposing to amend the regulation authorizing a health claim on the relationship between calcium and a reduced risk of osteoporosis to: Include vitamin D so that, in addition to claims for calcium and osteoporosis, additional claims can be made for calcium and vitamin D and osteoporosis; eliminate the
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3344. Food Labeling: Nutrient Content Claims, General Principles; Health Claims, General Requirements and Other Specific

PROPOSED RULES: Nutrient content claims; general principles; withdrawn in part,

The Food and Drug Administration (FDA) is announcing that it is withdrawing certain proposed amendments of a proposed rule that published in the Federal Register of December 21, 1995 (60 FR 66206), related to the calcium and osteoporosis health claim (21 CFR 101.72). FDA is taking action in response to a health claim petition submitted by The
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3345. Supplements and Other Changes to an Approved Application; Public Meeting

NOTICES: Supplements; chemistry, manufacturing, controls, and changes to approved marketing applications,

The Food and Drug Administration (FDA) is announcing a public meeting to solicit comments on issues that FDA should consider when developing revisions to its regulations regarding chemistry, manufacturing, and controls (CMC) supplements and other changes to approved marketing applications for human drugs. FDA is evaluating how it could revise its
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3346. Oral Dosage Form New Animal Drugs; Clomipramine Tablets

RULES: Clomipramine tablets,

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Novartis Animal Health US, Inc. The supplemental NADA adds a 5milligram tablet size of clomipramine hydrochloride, used in dogs for treatment of separation anxiety.
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3347. National Institute of Nursing Research; Notice of Meeting

NOTICES: National Institute of Nursing Research,

Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. Appendix 2), notice is hereby given of a meeting of the National Institute of Nursing Research.

The meeting will be open to the public as indicated below, with attendance limited to space available. Individuals who plan to attend and need special

DEPARTMENT OF HEALTH AND HUMAN SERVICES : National Institutes of Health

3348. Implantation or Injectable Dosage Form New Animal Drugs; Dexmedetomidine

RULES: Dexmedetomidine,

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an original new animal drug application (NADA) filed by Orion Corp. The NADA provides for veterinary prescription use of dexmedetomidine hydrochloride injectable solution as a sedative, analgesic, and preanesthetic in dogs.
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3349. Oral Dosage Form New Animal Drugs; Dirlotapide

RULES: Dirlotapide solution,

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a new animal drug application (NADA) filed by Pfizer, Inc. The NADA provides for the veterinary prescription use of dirlotapide solution in dogs for the management of obesity.
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

3350. Implantation or Injectable Dosage Form New Animal Drugs; Doxapram

RULES: Doxapram,

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 Modern Veterinary Therapeutics, LLC. The ANADA provides for the use of doxapram hydrochloride injectable solution in dogs, cats, and horses to stimulate respiration during and after
DEPARTMENT OF HEALTH AND HUMAN SERVICES : Food and Drug Administration

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