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NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-09
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
NOTICES: Migrant Health National Advisory Council,
Published: 2007-01-09
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,
PROPOSED RULES: Food labeling—; Conventional foods being marketed as functional foods; hearing,
Published: 2007-01-08
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
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-08
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
NOTICES: International Conference on Harmonisation—; Pharmacogenomics; E15 terminology,
Published: 2007-01-08
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availability of a draft guidance entitled ``E15 Terminology in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 The draft guidance was prepared under the auspices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The draft guidance
NOTICES: Minority Health Advisory Committee,
Published: 2007-01-08
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
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-08
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
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-08
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
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-08
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
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-08
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
RULES: Monensin,
Published: 2007-01-08
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
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-05
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
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-05
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
NOTICES: National Center for Environmental Health/Agency for Toxic Substances and Disease Registry—; Scientific Counselors Board,
Published: 2007-01-05
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.
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-05
NOTICES: Agency information collection activities; proposals, submissions, and approvals,
Published: 2007-01-05
NOTICES: Hospital inpatient prospective payment systems and 2007 FY rates; correction,
Published: 2007-01-05
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.
PROPOSED RULES: Food labeling—; Calcium, vitamin D, and osteoporosis; nutrient content claims,
Published: 2007-01-05
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
PROPOSED RULES: Nutrient content claims; general principles; withdrawn in part,
Published: 2007-01-05
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
NOTICES: Supplements; chemistry, manufacturing, controls, and changes to approved marketing applications,
Published: 2007-01-05
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
RULES: Clomipramine tablets,
Published: 2007-01-04
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.
NOTICES: National Institute of Nursing Research,
Published: 2007-01-04
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
RULES: Dexmedetomidine,
Published: 2007-01-04
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.
RULES: Dirlotapide solution,
Published: 2007-01-04
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.
RULES: Doxapram,
Published: 2007-01-04
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