Proposed Information Collection Activity; Comment Request, 49817-49818 [2012-20207]
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49817
Federal Register / Vol. 77, No. 160 / Friday, August 17, 2012 / Notices
[FR Doc. 2012–20074 Filed 8–16–12; 8:45 am]
BILLING CODE 4120–01–C
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Federal Child Support Services
Portal Registration.
OMB No.: 0970–0370.
The purpose of the Federal Child
Support Services Portal Registration is
to collect information from an
authorized individual registering to use
the Federal Parent Locator Service
(FPLS) Child Support Services Portal.
This information collection is necessary
to authenticate the individual’s identity
and comply with the statutory
requirement that federal Office of Child
Support Enforcement (OCSE) establish
and implement safeguards to restrict
access to confidential information in the
FPLS to authorized persons. 42 U.S.C.
653(m)(2).
After identity is authenticated, secure
accounts will be created for authorized
users to view data for their respective
applications.
Respondents: Employers, Financial
Institutions, Insurers, State Agencies,
Local Access and Visitation Providers.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Registration Screen .........................................................................................
588
1
0.1
58.8
Estimated Total Annual Burden
Hours: 58.8
Additional Information: Copies of the
proposed collection may be obtained by
writing to The Administration for
Children and Families, Office of
Information Services, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
OMB Comment: 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, 725 17th Street NW.,
Washington, DC 20503, Attn: Desk
Officer for ACF.
Bob Sargis,
Reports Clearance, Officer.
[FR Doc. 2012–20164 Filed 8–16–12; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: DHHS/ACF/OPRE Head Start
Classroom-based Approaches and
Resources for Emotion and Social skill
promotion (CARES) project: Tracking
Participants.
OMB No.: 0970–0364.
Description: The Head Start
Classroom-based Approaches and
Resources for Emotion and Social skill
promotion (CARES) project is an
evaluation of three social emotional
program enhancements within Head
Start settings serving three- and fouryear-old children. This project focuses
on identifying the central features of
effective programs to provide the
information federal policy makers and
Head Start providers will need if they
are to increase Head Start’s capacity to
improve the social and emotional skills
and school readiness of preschool age
children. The Head Start CARES project
completed data collection for cohort (1)
4-year-olds and cohort (2) 3-year-olds in
spring of 2011 and cohort (2) 4-year-olds
in the spring of 2012.
ACF is proposing to collect
information necessary to identify
CARES study respondents’ current
location and follow-up with
respondents until the children reach
third grade. In support of an
examination of third grade outcomes,
information must be collected from
parents or guardians until the third
grade year. Therefore, in the spring of
2013 tracking of all children will be
necessary, in the spring of 2014 for the
three- and four-year-old children in
cohort 2 only, and in the spring of 2015
the three-year-olds in cohort 2 only. To
enable the opportunity to conduct data
collection in 3rd grade, complete
tracking information on the full sample,
both ages and cohorts, for all years until
third grade is necessary. In addition to
location and contact information, a
small set of additional items will
provide information on the parents’
perception of the children’s well-being.
Respondents: The respondents to the
tracking phone calls will be low-income
parents and their Head Start children.
This is a three-year information
collection request.
ANNUAL BURDEN ESTIMATES
Annual
number of
respondents
erowe on DSK2VPTVN1PROD with NOTICES
Instrument
Number of
responses per
respondent
Average
burden hours
per response
Estimated
annual
burden hours
Parent Survey Cohort 1–4 year olds ...............................................................
Parent Survey Cohort 2–4 year olds ...............................................................
Parent Survey Cohort 2–3 year olds ...............................................................
201
690
320
1
2
3
0.33
0.33
0.33
66
1380
106
Total ..........................................................................................................
........................
........................
........................
1552
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E:\FR\FM\17AUN1.SGM
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49818
Federal Register / Vol. 77, No. 160 / Friday, August 17, 2012 / Notices
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
Email address:
OPREinfocollection@acf.hhs.gov. All
requests should be identified by the title
of the information collection.
The Department specifically requests
comments on (a) whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
ACF Reports Clearance Officer.
[FR Doc. 2012–20207 Filed 8–16–12; 8:45 am]
BILLING CODE 4184–22–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0873]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Bar Code Label
Requirement for Human Drug and
Biological Products
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
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
erowe on DSK2VPTVN1PROD with NOTICES
SUMMARY:
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concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the bar code label requirements for
human drug and biological products.
DATES: Submit either electronic or
written comments on the collection of
information by October 16, 2012.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT: Ila
Mizrachi, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
7726, ila.mizrachi@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
Agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
Agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’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 to be collected; and (4)
ways to minimize the burden of the
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collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Bar Code Label Requirement for
Human Drug and Biological Products—
(OMB Control Number 0910–0537)—
Extension
In the Federal Register of February
26, 2004 (69 FR 9120), we issued
regulations that required human drug
product and biological product labels to
have bar codes. The rule required bar
codes on most human prescription drug
products and on over-the-counter (OTC)
drug products that are dispensed under
an order and commonly used in health
care facilities. The rule also required
machine-readable information on blood
and blood components. For human
prescription drug products and OTC
drug products that are dispensed under
an order and commonly used in health
care facilities, the bar code must contain
the National Drug Code number for the
product. For blood and blood
components, the rule specifies the
minimum contents of the machinereadable information in a format
approved by the Center for Biologics
Evaluation and Research Director as
blood centers have generally agreed
upon the information to be encoded on
the label. The rule is intended to help
reduce the number of medication errors
in hospitals and other health care
settings by allowing health care
professionals to use bar code scanning
equipment to verify that the right drug
(in the right dose and right route of
administration) is being given to the
right patient at the right time.
Most of the information collection
burden resulting from the final rule, as
calculated in table 1 of the final rule (69
FR at 9149), was a one-time burden that
does not occur after the rule’s
compliance date of April 26, 2006. In
addition, some of the information
collection burden estimated in the final
rule is now covered in other OMBapproved information collection
packages for FDA. However, parties may
continue to seek an exemption from the
bar code requirement under certain,
limited circumstances. Section
201.25(d) (21 CFR 201.25(d)) requires
submission of a written request for an
exemption and describes the contents of
such requests. Based on the number of
exemption requests we have received,
we estimate that approximately 2
exemption requests may be submitted
annually, and that each exemption
request will require 24 hours to
complete. This would result in an
annual reporting burden of 48 hours.
E:\FR\FM\17AUN1.SGM
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]]>Agencies
[Federal Register Volume 77, Number 160 (Friday, August 17, 2012)]
[Notices]
[Pages 49817-49818]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-20207]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Title: DHHS/ACF/OPRE Head Start Classroom-based Approaches and
Resources for Emotion and Social skill promotion (CARES) project:
Tracking Participants.
OMB No.: 0970-0364.
Description: The Head Start Classroom-based Approaches and
Resources for Emotion and Social skill promotion (CARES) project is an
evaluation of three social emotional program enhancements within Head
Start settings serving three- and four-year-old children. This project
focuses on identifying the central features of effective programs to
provide the information federal policy makers and Head Start providers
will need if they are to increase Head Start's capacity to improve the
social and emotional skills and school readiness of preschool age
children. The Head Start CARES project completed data collection for
cohort (1) 4-year-olds and cohort (2) 3-year-olds in spring of 2011 and
cohort (2) 4-year-olds in the spring of 2012.
ACF is proposing to collect information necessary to identify CARES
study respondents' current location and follow-up with respondents
until the children reach third grade. In support of an examination of
third grade outcomes, information must be collected from parents or
guardians until the third grade year. Therefore, in the spring of 2013
tracking of all children will be necessary, in the spring of 2014 for
the three- and four-year-old children in cohort 2 only, and in the
spring of 2015 the three-year-olds in cohort 2 only. To enable the
opportunity to conduct data collection in 3rd grade, complete tracking
information on the full sample, both ages and cohorts, for all years
until third grade is necessary. In addition to location and contact
information, a small set of additional items will provide information
on the parents' perception of the children's well-being.
Respondents: The respondents to the tracking phone calls will be
low-income parents and their Head Start children. This is a three-year
information collection request.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Annual number Number of Average Estimated
Instrument of responses per burden hours annual burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
Parent Survey Cohort 1-4 year olds.............. 201 1 0.33 66
Parent Survey Cohort 2-4 year olds.............. 690 2 0.33 1380
Parent Survey Cohort 2-3 year olds.............. 320 3 0.33 106
---------------------------------------------------------------
Total....................................... .............. .............. .............. 1552
----------------------------------------------------------------------------------------------------------------
[[Page 49818]]
In compliance with the requirements of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Planning, Research and Evaluation, 370 L'Enfant Promenade SW.,
Washington, DC 20447, Attn: ACF Reports Clearance Officer. Email
address: OPREinfocollection@acf.hhs.gov. All requests should be
identified by the title of the information collection.
The Department specifically requests comments on (a) whether the
proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
ACF Reports Clearance Officer.
[FR Doc. 2012-20207 Filed 8-16-12; 8:45 am]
BILLING CODE 4184-22-P
