Proposed Collection; Comment Request; Parental Knowledge, Attitudes, and Behaviors Related to Pediatric Cardiovascular Health, 37713-37714 [E9-18071]
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37713
Federal Register / Vol. 74, No. 144 / Wednesday, July 29, 2009 / Notices
Seleda Perryman,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. E9–18016 Filed 7–28–09; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: State Plan for Foster Care and
Adoption Assistance—Title IV–E.
OMB No.: 0980–0141.
Description: A title IV–E plan is
required by section 471 part IV–E of the
Social Security Act (the Act) for each
public child welfare agency requesting
Federal funding for foster care, adoption
assistance and guardianship assistance
under the Act. The title IV–E plan
provides assurances the programs will
be administered in conformity with the
specific requirements stipulated in title
IV–E. The plan must include all
applicable State statutory, regulatory, or
policy references and citations for each
requirement as well as supporting
documentation. A title IV–E agency may
use the pre-print format prepared by the
Children’s Bureau of the Administration
for Children and Families or a different
format, on the condition that the format
used includes all of the title IV–E State
plan requirements of the law.
Public Law 110–351, the Fostering
Connections to Success and Increasing
Adoptions Act of 2008, created a new
title IV–E plan option to provide a
Guardianship Assistance Program for
relatives of children in foster care
(section 471(a)(28) of the Act). The
Guardianship Assistance program was
made effective for States upon
enactment of Public Law 110–351
(October 7, 2008).
Effective October 1, 2009, Public Law
110–351 will allow Tribes, Tribal
organizations and Tribal consortia to
directly operate title IV–E programs for
foster care maintenance payments,
adoption assistance and kinship
guardianship assistance.
The law also made a number of other
changes to title IV–E plan requirements
and eligibility criteria. The law’s
provisions expanding the scope of the
title IV–E program necessitates a
revision of the preprint.
Respondents: State and Territorial
Agencies (State Agencies) administering
or supervising the administration of the
title IV–E programs and Federallyrecognized Tribes, Tribal organizations
and Tribal consortia administering title
IV–E programs.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Title IV–E Plan .................................................................................................
33
1
16
528
Dated: July 23, 2009.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E9–17934 Filed 7–28–09; 8:45 am]
Estimated Total Annual Burden
Hours: 528.
Additional Information
BILLING CODE 4184–01–P
OMB Comment
mstockstill on DSKH9S0YB1PROD with NOTICES
Copies of the proposed collection may
be obtained by writing to the
Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the title of the information
collection. E-mail address:
infocollection@acf.hhs.gov.
SUMMARY: In compliance with the
requirement of section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
for opportunity for public comment on
proposed data collection projects, the
National Heart, Lung, and Blood
Institute (NHLBI), the National
Institutes of Health (NIH) will publish
periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
Proposed Collection: Describe the
proposed information collection activity
as follows. Include: Title: Parental
Knowledge, Attitudes, and Behaviors
Related to Pediatric Cardiovascular
Health; Type of Information Collection
Request: New; Need and Use of
OMB is required to make a decision
concerning the collection of information
between 30 and 60 days after
publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication. Written comments and
recommendations for the proposed
information collection should be sent
directly to the following: Office of
Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7245,
Attn: Desk Officer for the
Administration for Children and
Families.
VerDate Nov<24>2008
18:30 Jul 28, 2009
Jkt 217001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; Parental Knowledge,
Attitudes, and Behaviors Related to
Pediatric Cardiovascular Health
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Information Collection: Coinciding with
the release of the Integrated Pediatric
Cardiovascular Risk Reduction
Guidelines, the National Heart, Lung,
and Blood Institute (NHLBI) will
conduct a national public awareness
campaign to help parents understand
that risk for cardiovascular disease
(CVD) begins in childhood, and to
engage them in encouraging healthy
habits in their children to promote heart
health and reduce their children’s CVD
risk now and as they grow. Currently,
little is known about parental
knowledge, attitudes, and behaviors
related to heart health in children.
Serving as a baseline for evaluation of
NHLBI’s outreach activities related to
the campaign, this study seeks to learn
the following: (a) Parents’ awareness of
cardiovascular disease risk factors in
children and knowledge of what to do
for risk reduction, (b) parents’ level of
efficacy toward taking action to promote
cardiovascular health and reduce risk
factors, and (c) parents’ behaviors
related to cardiovascular health. The
findings will provide valuable
information that will enable NHLBI to
identify the gaps in knowledge and
awareness and target specific
information in communications with
parents. NHLBI will also be able to
determine parents’ efficacy related to
the actions needed to promote their
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37714
Federal Register / Vol. 74, No. 144 / Wednesday, July 29, 2009 / Notices
children’s heart health, allocating
resources for the campaign to provide
support to overcome perceived barriers;
Frequency of Response: One-time
survey; Affected Public: Individuals or
households; and Type of Respondents:
Parents and caregivers of children ages
0–7. The annual reporting burden is as
follows: Estimated Number of
Respondents: 1,175; Estimated Number
of Responses per Respondent: 1;
Average Burden Hours per Response:
.167; and Estimated Total Annual
Burden Hours Requested: 196.23. There
are no Capital Costs, Operating Costs
and/or Maintenance Costs to report.
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies should
address one or more of the following
points: (1) Evaluate 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) Evaluate 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) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) 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.
mstockstill on DSKH9S0YB1PROD with NOTICES
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact: Amy Pianalto,
National Heart, Lung, and Blood
Institute, NIH, 31 Center Drive, Building
31A, Room 4A10, Bethesda, MD 20892;
or call non-toll-free number 301–594–
2093 or e-mail request, including your
address, to pianaltoa@nhlbi.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60-days of the date of
this publication.
Dated: July 21, 2009.
Amy Pianalto,
Office of Communications and Legislative
Activities, NHLBI, National Institutes of
Health.
[FR Doc. E9–18071 Filed 7–28–09; 8:45 am]
BILLING CODE 4140–01–P
VerDate Nov<24>2008
18:30 Jul 28, 2009
Jkt 217001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0097]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Request for
Samples and Protocols
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: 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.
DATES: Fax written comments on the
collection of information by August 28,
2009.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–6974, or e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0206. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of Information
Management (HFA–710), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–796–3794.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Request for Samples and Protocols—
(OMB Control Number 0910–0206)—
Extension
Under section 351 of the Public
Health Service Act (42 U.S.C. 262), FDA
has the responsibility to issue
regulations that prescribe standards
designed to ensure the safety, purity,
and potency of biological products and
to ensure that the biologics licenses for
such products are only issued when a
product meets the prescribed standards.
Under § 610.2 (21 CFR 610.2), the
Center for Biologics Evaluation and
Research (CBER) or the Center for Drug
Evaluation and Research may at any
time require manufacturers of licensed
biological products to submit to FDA
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samples of any lot along with the
protocols showing the results of
applicable tests prior to distributing the
lot of the product. In addition to § 610.2,
there are other regulations that require
the submission of samples and protocols
for specific licensed biological products:
§§ 660.6 (21 CFR 660.6) (Antibody to
Hepatitis B Surface Antigen); 660.36 (21
CFR 660.36) (Reagent Red Blood Cells);
and 660.46 (21 CFR 660.46) (Hepatitis B
Surface Antigen). Section 660.6(a)
provides requirements for the frequency
of submission of samples from each lot
of Antibody to Hepatitis B Surface
Antigen product, and § 660.6(b)
provides the requirements for the
submission of a protocol containing
specific information along with each
required sample. For § 660.6 products
subject to official release by FDA, one
sample from each filling of each lot is
required to be submitted along with a
protocol consisting of a summary of the
history of manufacture of the product,
including all results of each test for
which test results are requested by
CBER. After official release is no longer
required, one sample along with a
protocol is required to be submitted at
90-day intervals. In addition, samples,
which must be accompanied by a
protocol, may at any time be required to
be submitted to CBER if continued
evaluation is deemed necessary.
Section 660.36(a) requires, after each
routine establishment inspection by
FDA, the submission of samples from a
lot of final Reagent Red Blood Cell
product along with a protocol
containing specific information. Section
660.36(a)(2) requires that a protocol
contain information including, but not
limited to, manufacturing records,
certain test records, and identity test
results. Section 660.36(b) requires a
copy of the antigenic constitution
matrix specifying the antigens present
or absent to be submitted to the CBER
Director at the time of initial
distribution of each lot. Section
660.46(a) contains requirements as to
the frequency of submission of samples
from each lot of Hepatitis B Surface
Antigen product, and § 660.46(b)
contains the requirements as to the
submission of a protocol containing
specific information along with each
required sample. For § 660.46 products
subject to official release by FDA, one
sample from each filling of each lot is
required to be submitted along with a
protocol consisting of a summary of the
history of manufacture of the product,
including all results of each test for
which test results are requested by
CBER. After notification of official
release is received, one sample along
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]]>Agencies
[Federal Register Volume 74, Number 144 (Wednesday, July 29, 2009)]
[Notices]
[Pages 37713-37714]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-18071]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment Request; Parental Knowledge,
Attitudes, and Behaviors Related to Pediatric Cardiovascular Health
SUMMARY: In compliance with the requirement of section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995, for opportunity for public comment
on proposed data collection projects, the National Heart, Lung, and
Blood Institute (NHLBI), the National Institutes of Health (NIH) will
publish periodic summaries of proposed projects to be submitted to the
Office of Management and Budget (OMB) for review and approval.
Proposed Collection: Describe the proposed information collection
activity as follows. Include: Title: Parental Knowledge, Attitudes, and
Behaviors Related to Pediatric Cardiovascular Health; Type of
Information Collection Request: New; Need and Use of Information
Collection: Coinciding with the release of the Integrated Pediatric
Cardiovascular Risk Reduction Guidelines, the National Heart, Lung, and
Blood Institute (NHLBI) will conduct a national public awareness
campaign to help parents understand that risk for cardiovascular
disease (CVD) begins in childhood, and to engage them in encouraging
healthy habits in their children to promote heart health and reduce
their children's CVD risk now and as they grow. Currently, little is
known about parental knowledge, attitudes, and behaviors related to
heart health in children. Serving as a baseline for evaluation of
NHLBI's outreach activities related to the campaign, this study seeks
to learn the following: (a) Parents' awareness of cardiovascular
disease risk factors in children and knowledge of what to do for risk
reduction, (b) parents' level of efficacy toward taking action to
promote cardiovascular health and reduce risk factors, and (c) parents'
behaviors related to cardiovascular health. The findings will provide
valuable information that will enable NHLBI to identify the gaps in
knowledge and awareness and target specific information in
communications with parents. NHLBI will also be able to determine
parents' efficacy related to the actions needed to promote their
[[Page 37714]]
children's heart health, allocating resources for the campaign to
provide support to overcome perceived barriers; Frequency of Response:
One-time survey; Affected Public: Individuals or households; and Type
of Respondents: Parents and caregivers of children ages 0-7. The annual
reporting burden is as follows: Estimated Number of Respondents: 1,175;
Estimated Number of Responses per Respondent: 1; Average Burden Hours
per Response: .167; and Estimated Total Annual Burden Hours Requested:
196.23. There are no Capital Costs, Operating Costs and/or Maintenance
Costs to report.
Request for Comments: Written comments and/or suggestions from the
public and affected agencies should address one or more of the
following points: (1) Evaluate 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) Evaluate 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) Enhance the
quality, utility, and clarity of the information to be collected; and
(4) 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.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact: Amy Pianalto, National Heart, Lung, and Blood
Institute, NIH, 31 Center Drive, Building 31A, Room 4A10, Bethesda, MD
20892; or call non-toll-free number 301-594-2093 or e-mail request,
including your address, to pianaltoa@nhlbi.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 60-days
of the date of this publication.
Dated: July 21, 2009.
Amy Pianalto,
Office of Communications and Legislative Activities, NHLBI, National
Institutes of Health.
[FR Doc. E9-18071 Filed 7-28-09; 8:45 am]
BILLING CODE 4140-01-P
