Statement of Organization, Functions, and Delegations of Authority; National Institutes of Health, 23817-23818 [2011-10318]
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23817
Federal Register / Vol. 76, No. 82 / Thursday, April 28, 2011 / Notices
June 30, 2011. We are requesting a
three-year clearance of this collection.
The 4040–0001 proposed collection
encompasses 14 forms.
There are four requested changes to
the SF 424 (R&R) Application for
Federal Assistance (Cover) and, there
are four requested changes to the R&R
Other Project Information form.
These changes to the instructions will
increase data quality and clarity for the
collection. Agencies will not be required
to collect all of the information in the
proposed data set. The agency will
identify the data that must be provided
by applicants through instructions that
will accompany the application forms.
ESTIMATED ANNUALIZED BURDEN TABLE FOR SF–424 R&R
Agency
DHS .......................
DOC ......................
DOD ......................
DOE ......................
DOI ........................
DOT .......................
ED .........................
HHS .......................
NARA ....................
NASA ....................
NRC ......................
NSF .......................
USAID ...................
USDA ....................
Total ...............
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Grant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Applicant
Average burden
on respondent per
response in hours
Total burden
hours
173
165
17,943
7,292
41
370
2,000
62,133
1
102
2
1,001
9
6,349
1
1
1
1
1
1
1
1
1
1
1
1
1
1
60
60
60
60
60
60
60
60
60
60
60
60
60
60
10,380
9,900
1,076,580
437,520
2,460
22,200
120,000
3,727,980
60
6,120
120
60,060
540
380,940
...............................................................
97,581
..............................
..............................
5,854,860
[FR Doc. 2011–10250 Filed 4–27–11; 8:45 am]
BILLING CODE 4151–AE–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Statement of Organization, Functions,
and Delegations of Authority; National
Institutes of Health
srobinson on DSKHWCL6B1PROD with NOTICES
Number of
responses per
respondent
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Mary Forbes,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
Part N, National Institutes of Health,
of the Statement of Organization,
Functions, and Delegations of Authority
for the Department of Health and
Human Services (40 FR 22859, May 27,
1975, as amended most recently at 66
FR 6617, January 22, 2001, and
redesignated from Part HN as Part N at
60 FR 56605, November 9, 1995), is
amended as set forth below to establish
the Division of the National Toxicology
Program (NTP) within the National
Institute of Environmental Health
Sciences (NIEHS).
Section N–V, Organization and
Functions, is amended as follows:
Immediately after the paragraph
headed ‘‘Office of Translational
Research’’ (N V4, formerly HN V4),
insert the following:
Division of the National Toxicology
Program (N V5, formerly HN V5). (1)
Provides toxicological evaluations on
substances of public health concern; (2)
develops and validates improved
toxicology methods (more sensitive,
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Number of annual
respondents
Type of respondent
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specific, and rapid); (3) develops
approaches and generates data to
strengthen the science base for risk
assessments; and (4) communicates
results with all stakeholders. Program
goals are achieved through a highly
integrated, cooperative research and
testing program carried out through inhouse research, research and
development contracts, cooperative
agreements, and other support
mechanisms.
Biomolecular Screening Branch (N
V52, formerly HN V52). (1) Develops
research and testing activities in high
and medium throughput screening
assays for rapid detection of biological
activities of significance to toxicology
and carcinogenesis, (2) carries out the
NTP automated screening assays with C.
elegans, (3) develops analysis tools and
approaches to allow an integrated
assessment of high throughput
screening endpoints and associations
with findings from traditional
toxicology and cancer models, and (4)
develops assays and approaches to
understand the genetic and epigenetic
bases for differences in susceptibility.
Cellular and Molecular Pathology
Branch (N V53, formerly HN V53).
Responsible for (1) managing,
evaluating, reviewing, and reporting all
pathology data generated through
conduct of NTP toxicity and
carcinogenicity studies; (2) establishing
standards, terminology, and diagnostic
criteria for rodent pathology; (3)
providing laboratory animal medicine
support for the NTP and Division of
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
Intramural Research (DIR); (4)
maintaining the NTP Archives; and (5)
managing pathology, toxicology, and
other contracts to support NTP and DIR
investigators. Staff veterinary scientists
provide collaborative pathology
diagnostic support for DIR investigators
and mentoring/training in toxicologic
pathology and laboratory animal
medicine.
Program Operations Branch (N V54,
formerly HN V54). (1) Provides
recommendations to the NTP for
scientific, administrative, and fiscal
procedures and requirements by which
NTP goals may be accomplished
through in-house and contract activities;
(2) provides resources for analytical
chemistry, toxicokinetics, and
evaluations of bioavailability and
biotransformation; (3) initiates the
contract award process and participates
with the NIEHS contracts office in the
review and award of the contract; (5)
manages toxicity and carcinogenicity
studies performed under contract and
monitors them for technical and fiscal
performance; (6) manages the receipt,
maintenance, tracking, and
dissemination of NTP documents and
data.
Toxicology Branch (N V55, formerly
HN V55). (1) Responsible for the design,
interpretation, review, and reporting of
general toxicology and carcinogenicity
studies, usually in rodent models, as
well as studies to evaluate targeted
effects on the immune system,
reproduction, development, and
interference with chromosomes and
E:\FR\FM\28APN1.SGM
28APN1
23818
Federal Register / Vol. 76, No. 82 / Thursday, April 28, 2011 / Notices
DNA for substances studied by the NTP;
(2) integrates information derived from
studies of absorption, metabolism,
distribution, and excretion of test
substances within the body and the
development of mathematical models
that utilize this information in the
extrapolation and prediction of findings
across different species and exposure
conditions; (3) oversees analysis and
development of models using
information derived from studies of
gene expression in different tissues; (4)
incorporates systems biology
approaches; (5) reports results from all
these specialized toxicology studies; (6)
develops new methodologies for
toxicological assessments; and (7)
provides guidance on the proper
utilization of new types of toxicology
information in hazard identification,
hazard characterization, and regulatory
decision-making.
NTP Laboratory (NTPL) (N V56,
formerly, HN V56). Responsible for
providing laboratory capabilities and
support for the performance of agentspecific, targeted research directly
related to specific substances nominated
to the NTP, issues of central importance
to programs of the NTP, or the
development of new methods to
advance the scientific programs of the
NTP.
Delegations of Authority Statement:
All delegations and redelegations of
authority to officers and employees of
NIH that were in effect immediately
prior to the effective date of this
reorganization and are consistent with
this reorganization shall continue in
effect, pending further redelegation.
Dated: April 20, 2011.
Francis S. Collins,
Director.
[FR Doc. 2011–10318 Filed 4–27–11; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–11–10GI]
Agency Forms Undergoing Paperwork
Reduction Act Review
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) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Evaluating Act Against AIDS Social
Marketing Campaign Phases Targeting
Consumers—New—National Center for
HIV/AIDS, Viral Hepatitis, STD and TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In response to the continued HIV
epidemic in our country, CDC has
launched Act Against AIDS (AAA), a 5year, multifaceted communication
campaign to reduce HIV incidence in
the United States. CDC plans to release
the campaign in phases, with some of
the phases running concurrently. Each
phase of the campaign will use mass
media and direct-to-consumer channels
to deliver HIV prevention and testing
messages. Some components of the
campaign will be designed to provide
basic education and increase awareness
of HIV/AIDS among the general public,
and others will be targeted to specific
subgroups or communities at greatest
risk of infection. The current study
addresses the need to assess the
effectiveness of these social marketing
messages aimed at increasing HIV
awareness and delivering HIV
prevention and testing messages among
at-risk populations.
This study will evaluate the AAA
social marketing campaign aimed at
increasing HIV/AIDS awareness,
increasing prevention behaviors, and
improving HIV testing rates among
consumers. The study will consist of a
quarterly tracking survey of AAA target
audiences to measure exposure to each
phase of the campaign and interventions
implemented under AAA. Each
extended survey will have a core set of
items asked in all rounds, as well as a
module of questions relating to specific
AAA activities and communication
initiatives that are occurring during a
given quarter. Each extended survey
sample will consist of 1,000
respondents selected from a
combination of sources, including a
national opt-in e-mail list sample and
respondent lists generated by
partnership organizations (e.g., the
National Urban League, the National
Medical Association). Participants will
self-administer the extended survey at
home on personal computers. The
research will include 12 data collections
over a 3-year period: four selfadministered quarterly extended
surveys per year over 3 years, with a
total of 12,000 respondents. There is no
cost to the respondents other than their
time. The total estimated annual burden
hours are 2667.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Form name
Individuals (male and female) aged 18 years
and older/Study Screener.
Individuals (male and female) aged 18 years
and older.
srobinson on DSKHWCL6B1PROD with NOTICES
Respondents
Study Screener ..............................................
20,000
1
2/60
Extended survey ............................................
4,000
1
30/60
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Agencies
[Federal Register Volume 76, Number 82 (Thursday, April 28, 2011)]
[Notices]
[Pages 23817-23818]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-10318]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Statement of Organization, Functions, and Delegations of
Authority; National Institutes of Health
Part N, National Institutes of Health, of the Statement of
Organization, Functions, and Delegations of Authority for the
Department of Health and Human Services (40 FR 22859, May 27, 1975, as
amended most recently at 66 FR 6617, January 22, 2001, and redesignated
from Part HN as Part N at 60 FR 56605, November 9, 1995), is amended as
set forth below to establish the Division of the National Toxicology
Program (NTP) within the National Institute of Environmental Health
Sciences (NIEHS).
Section N-V, Organization and Functions, is amended as follows:
Immediately after the paragraph headed ``Office of Translational
Research'' (N V4, formerly HN V4), insert the following:
Division of the National Toxicology Program (N V5, formerly HN V5).
(1) Provides toxicological evaluations on substances of public health
concern; (2) develops and validates improved toxicology methods (more
sensitive, specific, and rapid); (3) develops approaches and generates
data to strengthen the science base for risk assessments; and (4)
communicates results with all stakeholders. Program goals are achieved
through a highly integrated, cooperative research and testing program
carried out through in-house research, research and development
contracts, cooperative agreements, and other support mechanisms.
Biomolecular Screening Branch (N V52, formerly HN V52). (1)
Develops research and testing activities in high and medium throughput
screening assays for rapid detection of biological activities of
significance to toxicology and carcinogenesis, (2) carries out the NTP
automated screening assays with C. elegans, (3) develops analysis tools
and approaches to allow an integrated assessment of high throughput
screening endpoints and associations with findings from traditional
toxicology and cancer models, and (4) develops assays and approaches to
understand the genetic and epigenetic bases for differences in
susceptibility.
Cellular and Molecular Pathology Branch (N V53, formerly HN V53).
Responsible for (1) managing, evaluating, reviewing, and reporting all
pathology data generated through conduct of NTP toxicity and
carcinogenicity studies; (2) establishing standards, terminology, and
diagnostic criteria for rodent pathology; (3) providing laboratory
animal medicine support for the NTP and Division of Intramural Research
(DIR); (4) maintaining the NTP Archives; and (5) managing pathology,
toxicology, and other contracts to support NTP and DIR investigators.
Staff veterinary scientists provide collaborative pathology diagnostic
support for DIR investigators and mentoring/training in toxicologic
pathology and laboratory animal medicine.
Program Operations Branch (N V54, formerly HN V54). (1) Provides
recommendations to the NTP for scientific, administrative, and fiscal
procedures and requirements by which NTP goals may be accomplished
through in-house and contract activities; (2) provides resources for
analytical chemistry, toxicokinetics, and evaluations of
bioavailability and biotransformation; (3) initiates the contract award
process and participates with the NIEHS contracts office in the review
and award of the contract; (5) manages toxicity and carcinogenicity
studies performed under contract and monitors them for technical and
fiscal performance; (6) manages the receipt, maintenance, tracking, and
dissemination of NTP documents and data.
Toxicology Branch (N V55, formerly HN V55). (1) Responsible for the
design, interpretation, review, and reporting of general toxicology and
carcinogenicity studies, usually in rodent models, as well as studies
to evaluate targeted effects on the immune system, reproduction,
development, and interference with chromosomes and
[[Page 23818]]
DNA for substances studied by the NTP; (2) integrates information
derived from studies of absorption, metabolism, distribution, and
excretion of test substances within the body and the development of
mathematical models that utilize this information in the extrapolation
and prediction of findings across different species and exposure
conditions; (3) oversees analysis and development of models using
information derived from studies of gene expression in different
tissues; (4) incorporates systems biology approaches; (5) reports
results from all these specialized toxicology studies; (6) develops new
methodologies for toxicological assessments; and (7) provides guidance
on the proper utilization of new types of toxicology information in
hazard identification, hazard characterization, and regulatory
decision-making.
NTP Laboratory (NTPL) (N V56, formerly, HN V56). Responsible for
providing laboratory capabilities and support for the performance of
agent-specific, targeted research directly related to specific
substances nominated to the NTP, issues of central importance to
programs of the NTP, or the development of new methods to advance the
scientific programs of the NTP.
Delegations of Authority Statement: All delegations and
redelegations of authority to officers and employees of NIH that were
in effect immediately prior to the effective date of this
reorganization and are consistent with this reorganization shall
continue in effect, pending further redelegation.
Dated: April 20, 2011.
Francis S. Collins,
Director.
[FR Doc. 2011-10318 Filed 4-27-11; 8:45 am]
BILLING CODE 4140-01-P