Submission for OMB Review; Comment Request New proposed collection, Biospecimen and Physical Measures Formative Research Methodology Studies for the National Children's Study, 54474-54476 [2011-22456]
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Federal Register / Vol. 76, No. 170 / Thursday, September 1, 2011 / Notices
heading of this document. Received
comments may be seen in the Division
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and 4 p.m., Monday through Friday.
III. Paperwork Reduction Act of 1995
This guidance refers to previously
approved collections of information
found in FDA regulations. These
collections of information are subject to
review by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3520). The collections of information in
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under OMB control number 0910–0001;
the collections of information required
on Form FDA–356h have been approved
under OMB control number 0910–0338;
and the collections of information
required on Form FDA–3397 have been
approved under OMB control number
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IV. Electronic Access
Persons with access to the Internet
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Dated: August 25, 2011.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2011–22373 Filed 8–31–11; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review;
Comment Request New proposed
collection, Biospecimen and Physical
Measures Formative Research
Methodology Studies for the National
Children’s Study
Under the provisions of
Section (3507(a)(1)(D)) of the Paperwork
Reduction Act of 1995, the National
Institutes of Health has submitted to the
Office of Management and Budget
(OMB) a request to review and approve
the information collection listed below.
This proposed information collection
was previously published in the Federal
SUMMARY:
Register on April 27, 2011, pages
23609–23611, and allowed 60 days for
public comment. Two written
comments and two verbal comments
were received. The verbal comments
expressed support for the broad scope of
the study. The written comments were
identical and questioned the cost and
utility of the study. The purpose of this
notice is to allow an additional 30 days
for public comment. The National
Institutes of Health may not conduct or
sponsor, and the respondent is not
required to respond to, an information
collection that has been extended,
revised, or implemented on or after
October 1, 1995, unless it displays a
currently valid OMB control number.
Proposed Collection: Title:
Biospecimen and Physical Measures
Formative Research Methodology
Studies for the National Children’s
Study (NCS). Type of Information
Request: NEW. Need and Use of
Information Collection: The Children’s
Health Act of 2000 (Pub. L. 106–310)
states:
(a) PURPOSE.—It is the purpose of this
section to authorize the National Institute of
Child Health and Human Development* to
conduct a national longitudinal study of
environmental influences (including
physical, chemical, biological, and
psychosocial) on children’s health and
development.
(b) IN GENERAL.—The Director of the
National Institute of Child Health and
Human Development* shall establish a
consortium of representatives from
appropriate Federal agencies (including the
Centers for Disease Control and Prevention,
the Environmental Protection Agency) to—
(1) plan, develop, and implement a
prospective cohort study, from birth to
adulthood, to evaluate the effects of both
chronic and intermittent exposures on child
health and human development; and
(2) investigate basic mechanisms of
developmental disorders and environmental
factors, both risk and protective, that
influence health and developmental
processes.
(c) REQUIREMENT.—The study under
subsection (b) shall—
(1) incorporate behavioral, emotional,
educational, and contextual consequences to
enable a complete assessment of the physical,
chemical, biological, and psychosocial
environmental influences on children’s wellbeing;
(2) gather data on environmental
influences and outcomes on diverse
populations of children, which may include
the consideration of prenatal exposures; and
(3) consider health disparities among
children, which may include the
consideration of prenatal exposures.
To fulfill the requirements of the
Children’s Health Act, the results of
formative research tests will be used to
maximize the efficiency (measured by
scientific robustness, participant and
infrastructure burden, and cost) of
biospecimen and physical measurement
collection procedures, accompanying
questionnaires, storage and information
management processes, and assay
procedures, thereby informing data
collection methodologies for the
National Children’s Study (NCS)
Vanguard and Main Studies. With this
submission, the NCS seeks to obtain
OMB’s generic clearance to conduct
formative research featuring
biospecimen and physical measurement
collections.
The results from these formative
research projects will inform the
feasibility (scientific robustness),
acceptability (burden to participants
and study logistics) and cost of NCS
Vanguard and Main Study biospecimen
collection procedures and physical
measurements in a manner that
minimizes public information collection
burden compared to burden anticipated
if these projects were incorporated
directly into either the NCS Vanguard or
Main Study. Frequency of Response:
Annual [As needed on an on-going and
concurrent basis]. Affected Public:
Members of the public, researchers,
practitioners, and other health
professionals. Type of Respondents:
Women of child-bearing age, infants,
children, fathers, health care facilities
and professionals, public health
professional organizations and
practitioners, and hospital
administrators. These include both
persons enrolled in the NCS Vanguard
Study and their peers who are not
participating in the NCS Vanguard
Study. Annual reporting burden: See
Table 1. The annualized cost to
respondents is estimated at: $600,000
(based on $10 per hour). There are no
Capital Costs to report. There are no
Operating or Maintenance Costs to
report.
srobinson on DSK4SPTVN1PROD with NOTICES
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN SUMMARY, BIOLOGICAL AND PHYSICAL MEASURES
Estimated
number of
respondents
Data collection activity
Type of respondent
Blood:
Adult ...........................................
NCS participants ..............................
VerDate Mar<15>2010
16:16 Aug 31, 2011
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PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
Estimated
number of
responses per
respondent
4,000
E:\FR\FM\01SEN1.SGM
1
01SEN1
Average
burden hours
per response
0.5
Estimated total
annual burden
hours
requested
2,000
54475
Federal Register / Vol. 76, No. 170 / Thursday, September 1, 2011 / Notices
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN SUMMARY, BIOLOGICAL AND PHYSICAL MEASURES—Continued
Data collection activity
Infant/Child .................................
Urine:
Adult ...........................................
Infant/Child .................................
Hair:
Adult ...........................................
Nails:
Adult ...........................................
Cervical Fluid:
Women .......................................
Breast Milk:
Women .......................................
Cord Blood:
Infant/ Child ................................
Meconium:
Infant/Child .................................
Placenta:
Infant ..........................................
Length:
Infant ..........................................
Height:
Child ...........................................
Weight:
Infant/Child .................................
Head Circumference:
Infant/Child .................................
Middle Upper Arm Circumference:
Infant/Child .................................
srobinson on DSK4SPTVN1PROD with NOTICES
Estimated
number of
respondents
Type of respondent
Ulnar Length:
Infant/Child .................................
Small, focused survey and instrument design and administration.
16:16 Aug 31, 2011
Average
burden hours
per response
Estimated total
annual burden
hours
requested
Members of NCS target population
(not NCS participants).
NCS participants ..............................
Members of NCS target population
(not NCS participants).
4,000
1
0.5
2,000
2,000
2,000
1
1
0.5
0.5
1,000
1,000
NCS participants ..............................
Members of NCS target population
(not NCS participants).
NCS participants ..............................
Members of NCS target population
(not NCS participants).
4,000
4,000
1
1
0.25
0.25
1,000
1,000
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
4,000
4,000
1
1
0.25
0.25
1,000
1,000
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
4,000
4,000
1
1
0.5
0.5
2,000
2,000
NCS participants ..............................
Members of NCS target population
(not NCS participants).
4,000
4,000
1
1
0.5
0.5
2,000
2,000
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
4,000
4,000
1
1
0.25
0.25
1000
1000
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
1
1
0.25
0.25
500
500
NCS participants ..............................
Members of NCS target population
(not NCS participants).
NCS participants ..............................
2,000
2,000
1
1
0.25
0.25
500
500
4,000
2
1
8,000
4,000
2
1
8,000
2,000
1
1
2,000
Members of NCS target population
(not NCS participants).
Health and Social Service Providers
VerDate Mar<15>2010
Estimated
number of
responses per
respondent
Jkt 223001
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
E:\FR\FM\01SEN1.SGM
01SEN1
54476
Federal Register / Vol. 76, No. 170 / Thursday, September 1, 2011 / Notices
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN SUMMARY, BIOLOGICAL AND PHYSICAL MEASURES—Continued
Data collection activity
Focus groups ....................................
Cognitive interviews ..........................
srobinson on DSK4SPTVN1PROD with NOTICES
Total ...........................................
16:16 Aug 31, 2011
Estimated
number of
responses per
respondent
Average
burden hours
per response
Estimated total
annual burden
hours
requested
Community Stakeholders .................
NCS participants ..............................
Members of NCS target population
(not NCS participants).
Health and Social Service Providers
Community Stakeholders .................
NCS participants ..............................
Members of NCS target population
(not NCS participants).
2,000
2,000
2,000
1
1
1
1
1
1
2,000
2,000
2,000
2,000
2,000
500
500
1
1
1
1
1
1
2
2
2,000
2,000
1,000
1,000
...........................................................
113,000
........................
........................
60,000
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Whether the proposed collection of
information is necessary for the proper
performance of the function of the
agency, including whether the
information will have practical utility;
(2) The accuracy of the agency’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information collected; and (4) Ways to
minimize the burden of the collection of
information on those who are to
respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to Office of
Management and Budget, Office of
Information and Regulatory Affairs,
Attn: NIH Desk Officer, by E-mail to
OIRA_submission@omb.eop.gov, or by
fax to 202–395–6974. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and instruments, contact Ms.
Jamelle E. Banks, Public Health Analyst,
Office of Science Policy, Analysis and
Communication, National Institute of
Child Health and Human Development,
31 Center Drive Room 2A18, Bethesda,
Maryland, 20892, or call a non-toll free
number (301) 496–1877 or E-mail your
request, including your address to
banksj@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
VerDate Mar<15>2010
Estimated
number of
respondents
Type of respondent
Jkt 223001
received within 30 days of the date of
this publication.
Dated: August 25, 2011.
Jamelle E. Banks,
Public Health Analyst, Office of Science
Policy, Analysis and Communications,
National Institute of Child Health and Human
Development.
[FR Doc. 2011–22456 Filed 8–31–11; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Diabetes and
Digestive and Kidney Diseases; Notice
of Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; NIDDK Ancillary
Studies to Major Ongoing Clinical Studies:
DCCT/EDIC.
Date: September 30, 2011.
Time: 2 p.m. to 3 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892, (Telephone
Conference Call).
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
Contact Person: Najma Begum, PhD,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 749, 6707 Democracy Boulevard,
Bethesda, MD 20892–5452, (301) 594–8894,
begumn@niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; R24 Seeding.
Date: October 5, 2011.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Bethesda Marriott Suites, 6711
Democracy Boulevard, Bethesda, MD 20817.
Contact Person: D.G. Patel, PhD, Scientific
Review Officer, Review Branch, DEA,
NIDDK, National Institutes of Health, Room
756, 6707 Democracy Boulevard, Bethesda,
MD 20892–5452, (301) 594–7682,
pateldg@niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; Novel Therapies for
NIDDM P01.
Date: October 14, 2011.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Bethesda Marriott Suites, 6711
Democracy Boulevard, Bethesda, MD 20817.
Contact Person: D.G. Patel, PhD, Scientific
Review Officer, Review Branch, DEA,
NIDDK, National Institutes of Health, Room
756, 6707 Democracy Boulevard, Bethesda,
MD 20892–5452, (301) 594–7682,
pateldg@niddk.nih.gov.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; Fellowships in
Digestive Diseases and Nutrition.
Date: October 18, 2011.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hotel Kabuki, 1625 Post Street, San
Francisco, CA 94115.
Contact Person: Thomas A. Tatham, PhD,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes of Health,
Room 760, 6707 Democracy Boulevard,
Bethesda, MD 20892–5452, (301) 594–3993.
tathamt@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.847, Diabetes,
E:\FR\FM\01SEN1.SGM
01SEN1
]]>Agencies
[Federal Register Volume 76, Number 170 (Thursday, September 1, 2011)]
[Notices]
[Pages 54474-54476]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-22456]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; Comment Request New proposed
collection, Biospecimen and Physical Measures Formative Research
Methodology Studies for the National Children's Study
SUMMARY: Under the provisions of Section (3507(a)(1)(D)) of the
Paperwork Reduction Act of 1995, the National Institutes of Health has
submitted to the Office of Management and Budget (OMB) a request to
review and approve the information collection listed below. This
proposed information collection was previously published in the Federal
Register on April 27, 2011, pages 23609-23611, and allowed 60 days for
public comment. Two written comments and two verbal comments were
received. The verbal comments expressed support for the broad scope of
the study. The written comments were identical and questioned the cost
and utility of the study. The purpose of this notice is to allow an
additional 30 days for public comment. The National Institutes of
Health may not conduct or sponsor, and the respondent is not required
to respond to, an information collection that has been extended,
revised, or implemented on or after October 1, 1995, unless it displays
a currently valid OMB control number.
Proposed Collection: Title: Biospecimen and Physical Measures
Formative Research Methodology Studies for the National Children's
Study (NCS). Type of Information Request: NEW. Need and Use of
Information Collection: The Children's Health Act of 2000 (Pub. L. 106-
310) states:
(a) PURPOSE.--It is the purpose of this section to authorize the
National Institute of Child Health and Human Development* to conduct
a national longitudinal study of environmental influences (including
physical, chemical, biological, and psychosocial) on children's
health and development.
(b) IN GENERAL.--The Director of the National Institute of Child
Health and Human Development* shall establish a consortium of
representatives from appropriate Federal agencies (including the
Centers for Disease Control and Prevention, the Environmental
Protection Agency) to--
(1) plan, develop, and implement a prospective cohort study,
from birth to adulthood, to evaluate the effects of both chronic and
intermittent exposures on child health and human development; and
(2) investigate basic mechanisms of developmental disorders and
environmental factors, both risk and protective, that influence
health and developmental processes.
(c) REQUIREMENT.--The study under subsection (b) shall--
(1) incorporate behavioral, emotional, educational, and
contextual consequences to enable a complete assessment of the
physical, chemical, biological, and psychosocial environmental
influences on children's well-being;
(2) gather data on environmental influences and outcomes on
diverse populations of children, which may include the consideration
of prenatal exposures; and
(3) consider health disparities among children, which may
include the consideration of prenatal exposures.
To fulfill the requirements of the Children's Health Act, the
results of formative research tests will be used to maximize the
efficiency (measured by scientific robustness, participant and
infrastructure burden, and cost) of biospecimen and physical
measurement collection procedures, accompanying questionnaires, storage
and information management processes, and assay procedures, thereby
informing data collection methodologies for the National Children's
Study (NCS) Vanguard and Main Studies. With this submission, the NCS
seeks to obtain OMB's generic clearance to conduct formative research
featuring biospecimen and physical measurement collections.
The results from these formative research projects will inform the
feasibility (scientific robustness), acceptability (burden to
participants and study logistics) and cost of NCS Vanguard and Main
Study biospecimen collection procedures and physical measurements in a
manner that minimizes public information collection burden compared to
burden anticipated if these projects were incorporated directly into
either the NCS Vanguard or Main Study. Frequency of Response: Annual
[As needed on an on-going and concurrent basis]. Affected Public:
Members of the public, researchers, practitioners, and other health
professionals. Type of Respondents: Women of child-bearing age,
infants, children, fathers, health care facilities and professionals,
public health professional organizations and practitioners, and
hospital administrators. These include both persons enrolled in the NCS
Vanguard Study and their peers who are not participating in the NCS
Vanguard Study. Annual reporting burden: See Table 1. The annualized
cost to respondents is estimated at: $600,000 (based on $10 per hour).
There are no Capital Costs to report. There are no Operating or
Maintenance Costs to report.
Table 1--Estimated Annual Reporting Burden Summary, Biological and Physical Measures
----------------------------------------------------------------------------------------------------------------
Estimated Estimated
Type of Estimated number of Average burden total annual
Data collection activity respondent number of responses per hours per burden hours
respondents respondent response requested
----------------------------------------------------------------------------------------------------------------
Blood:
Adult..................... NCS participants 4,000 1 0.5 2,000
[[Page 54475]]
Members of NCS 4,000 1 0.5 2,000
target
population (not
NCS
participants).
Infant/Child.............. NCS participants 2,000 1 0.5 1,000
Members of NCS 2,000 1 0.5 1,000
target
population (not
NCS
participants).
Urine:
Adult..................... NCS participants 4,000 1 0.25 1,000
Members of NCS 4,000 1 0.25 1,000
target
population (not
NCS
participants).
Infant/Child.............. NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Hair:
Adult..................... NCS participants 4,000 1 0.25 1,000
Members of NCS 4,000 1 0.25 1,000
target
population (not
NCS
participants).
Nails:
Adult..................... NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Cervical Fluid:
Women..................... NCS participants 4,000 1 0.5 2,000
Members of NCS 4,000 1 0.5 2,000
target
population (not
NCS
participants).
Breast Milk:
Women..................... NCS participants 4,000 1 0.5 2,000
Members of NCS 4,000 1 0.5 2,000
target
population (not
NCS
participants).
Cord Blood:
Infant/ Child............. NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Meconium:
Infant/Child.............. NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Placenta:
Infant.................... NCS participants 4,000 1 0.25 1000
Members of NCS 4,000 1 0.25 1000
target
population (not
NCS
participants).
Length:
Infant.................... NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Height:
Child..................... NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Weight:
Infant/Child.............. NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Head Circumference:
Infant/Child.............. NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Middle Upper Arm
Circumference:
Infant/Child.............. NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Ulnar Length:
Infant/Child.............. NCS participants 2,000 1 0.25 500
Members of NCS 2,000 1 0.25 500
target
population (not
NCS
participants).
Small, focused survey and NCS participants 4,000 2 1 8,000
instrument design and
administration.
Members of NCS 4,000 2 1 8,000
target
population (not
NCS
participants).
Health and 2,000 1 1 2,000
Social Service
Providers.
[[Page 54476]]
Community 2,000 1 1 2,000
Stakeholders.
Focus groups.................. NCS participants 2,000 1 1 2,000
Members of NCS 2,000 1 1 2,000
target
population (not
NCS
participants).
Health and 2,000 1 1 2,000
Social Service
Providers.
Community 2,000 1 1 2,000
Stakeholders.
Cognitive interviews.......... NCS participants 500 1 2 1,000
Members of NCS 500 1 2 1,000
target
population (not
NCS
participants).
Total..................... ................ 113,000 .............. .............. 60,000
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies are invited on one or more of the
following points: (1) Whether the proposed collection of information is
necessary for the proper performance of the function of the agency,
including whether the information will have practical utility; (2) The
accuracy of the agency's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (3) Ways to enhance the quality, utility, and
clarity of the information collected; and (4) Ways to minimize the
burden of the collection of information on those who are to respond,
including the use of appropriate automated, electronic, mechanical, or
other technological collection techniques or other forms of information
technology.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to Office of Management and Budget, Office of Information and
Regulatory Affairs, Attn: NIH Desk Officer, by E-mail to OIRA_submission@omb.eop.gov, or by fax to 202-395-6974. To request more
information on the proposed project or to obtain a copy of the data
collection plans and instruments, contact Ms. Jamelle E. Banks, Public
Health Analyst, Office of Science Policy, Analysis and Communication,
National Institute of Child Health and Human Development, 31 Center
Drive Room 2A18, Bethesda, Maryland, 20892, or call a non-toll free
number (301) 496-1877 or E-mail your request, including your address to
banksj@mail.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30 days
of the date of this publication.
Dated: August 25, 2011.
Jamelle E. Banks,
Public Health Analyst, Office of Science Policy, Analysis and
Communications, National Institute of Child Health and Human
Development.
[FR Doc. 2011-22456 Filed 8-31-11; 8:45 am]
BILLING CODE 4140-01-P
