Agency Information Collection Activities; Proposed Collection; Comment Request; Chronic Disease Self-Management Education Program Standardized Data Collection, 17214-17215 [2013-06390]
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Federal Register / Vol. 78, No. 54 / Wednesday, March 20, 2013 / Notices
Office of Child Support Enforcement,
was established pursuant to the
Personal Responsibility and Work
Opportunity Reconciliation Act of 1996.
42 U.S.C. 653(i)(1). In accordance with
section 453A(g)(2) of the Social Security
Act, employers are required to report
information pertaining to newly hired
employees to their state directory of
new hires (SDNH) and, within three
days of receiving employer information,
states are required to transmit SDNH
information to the NDNH. States are
also required to transmit wage and
unemployment compensation claims
information to the NDNH on a quarterly
basis. Federal agencies are required to
report new hires and quarterly wage
information directly to the NDNH.
The information maintained in the
NDNH is collected electronically and
assists states administering child
support programs locate parents and
enforce child support orders.
Additionally, Congress authorized
specific state and federal agencies to
receive NDNH information for
authorized purposes to assist in
administering certain programs.
Respondents: Employers, State Child
Support Enforcement Agencies, and
State Workforce Agencies.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Number of
responses per
respondent
New Hire: Employers Reporting Manually .................................................
1 5,294,970
2 1.98
New Hire: Employers Reporting Electronically ..........................................
3 635,162
4 76.40
New Hire: States ........................................................................................
54
6 193,947.41
Quarterly Wage & Unemployment Compensation .....................................
53
8 27
Multistate Employers’ Notification Form .....................................................
4,632
1
Total ....................................................................................................
........................
........................
Average burden
hours per
response
Total burden
hours
.025 hours (1.5
minutes).
.00028 hours (1
second) 5.
.016667 hours (1
minute) 7.
.00028 hours (2
minutes).
.050 hours (3 minutes).
262,101.02
.............................
450,477
13,587.39
174,556.16
.40
231.60
1 Eighty-nine
percent of all employers report manually (based on SSA’s experience).
the ‘‘Employers’’ tiers, ‘‘response’’ is defined as the number of new hire reports. Only 18 percent of all new hire reports are reported
manually and 82 percent are reported electronically (based on OCSE’s experience).
3 Eleven percent of all employers report electronically (based on SSA’s experience).
4 ‘‘Response’’ is defined as the number of new hire reports. Eighty-two percent of new hire reports are reported electronically (based on
OCSE’s experience).
5 Based on the assumption that employers reporting new hires electronically transmit their reports in a batch file, thus significantly reducing the
per-response burden.
6 Based on the average number of reports per transmission and the average burden per new hire report that are submitted manually. Reports
submitted electronically are automated. The average number of reports per transmission is calculated by dividing 10,473,160 (total number of
manual new hire reports) by 54 (total number of states).
7 The average burden per new hire report is estimated to be one minute.
8 ‘‘Response’’ is defined here as the number of transmissions to the NDNH. States are required to transmit quarterly wage and unemployment
compensation data four times a year.
2 For
Additional Information
Copies of the proposed collection may
be obtained 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. All
requests should be identified by the title
of the information collection. Email
address: infocollection@acf.hhs.gov.
Office of Management and Budget,
Paperwork Reduction Project, Fax:
202–395–7285, Email:
OIRA_SUBMISSION@OMB.EOP.GOV.
Attn: Desk Officer for the
Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
Estimated Total Annual Burden
Hours: 450,477 hours.
srobinson on DSK4SPTVN1PROD with NOTICES
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:
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18:04 Mar 19, 2013
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[FR Doc. 2013–06326 Filed 3–19–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Chronic Disease
Self-Management Education Program
Standardized Data Collection
Administration on Aging
(AoA), Administration for Community
Living (ACL), HHS.
AGENCY:
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ACTION:
Notice.
SUMMARY: The Administration on Aging
(AoA), now part of the Administration
for Community Living, is announcing
that the proposed collection of
information listed below has been
submitted to the Office of Management
and Budget (OMB) for review and
clearance under the Paperwork
Reduction Act of 1995.
DATES: Submit written comments on the
collection of information by April 19,
2013.
ADDRESSES: OIRA_submission@omb.
eop.gov or by fax to 202.395.5806. Attn:
OMB Desk Officer for ACL, Office of
Information and Regulatory Affairs,
OMB.
FOR FURTHER INFORMATION CONTACT:
Michele Boutaugh, 404–987–3411 or
Michele.boutaugh@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, the
Administration on Aging (now part of
the Administration for Community
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Federal Register / Vol. 78, No. 54 / Wednesday, March 20, 2013 / Notices
Living) has submitted the following
proposed collection of information to
OMB for review and clearance.
The ‘‘Empowering Older Adults and
Adults with Disabilities through
Chronic Disease Self-Management
Education (CDSME) Programs’’
cooperative agreement program is
financed through 2012 Prevention and
Public Health Funds. The proposed data
collection is necessary for monitoring
grant program operations and outcomes.
AoA proposes to gather information to
monitor grantee progress, record
location of sites where workshops are
held which will allow mapping of the
delivery infrastructure, and document
participant attendance and demographic
and health characteristics. The proposed
Participant Survey requests the
participants’ gender, zip code and
birthdate to allow for potential Medicare
claims matching and an analysis of
changes in health care utilization post
participation.
In response to the 60-day Federal
Register notice related to this proposed
data collection and published on July
23, 2013, four sets of comments were
received. Concern was expressed about
the collection of sensitive personal
information. Most of the remaining
comments provided suggestions for
enhancing the quality and clarity of the
information to be collected. The
comments resulted in some revisions to
the proposed data collection tools. The
originally proposed data collection
tools, the comments with responses and
a revised set of data collection tools may
be found on the AoA Web site at:
https://www.aoa.gov/AoARoot/
AoA_Programs/Tools_Resources/
collection_tools.aspx.
ACL estimates the burden of this
collection of information as 440 hours
for State Governments, 1050 hours for
local agency staff, and 2,500 hours for
individuals—Total burden is 3,990
hours per year.
Dated: March 15, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
[FR Doc. 2013–06390 Filed 3–19–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0242]
Agency Information Collection
Activities: Proposed Collection;
Comment Request; Current Good
Manufacturing Practice for Positron
Emission Tomography Drugs
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: 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 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 information collection contained in
FDA’s regulations on current good
manufacturing practice (CGMP) for
positron emission tomography (PET)
drugs.
DATES: Submit either electronic or
written comments on the collection of
information by May 20, 2013.
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
S. Mizrachi, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., P150–
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.
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17215
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
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Current Good Manufacturing Practice
for Positron Emission Tomography
Drugs—(OMB Control Number 0910–
0667)—Extension
Positron emission tomography is a
medical imaging modality involving the
use of a unique type of
radiopharmaceutical drug product.
FDA’s CGMP regulations at 21 CFR part
212 are intended to ensure that PET
drug products meet the requirements of
the Federal Food, Drug, and Cosmetic
Act (the FD&C Act) regarding safety,
identity, strength, quality, and purity.
The CGMP requirements for PET drugs
are issued under the provisions of the
Food and Drug Administration
Modernization Act (FDAMA). These
CGMP requirements are designed to take
into account the unique characteristics
of PET drugs, including their short halflives and the fact that most PET drugs
are produced at locations that are very
close to the patients to whom the drugs
are administered.
The CGMP regulations are intended to
ensure that approved PET drugs meet
the requirements of the FD&C Act as to
safety, identity, strength, quality, and
purity. The regulations address the
following matters: Personnel and
resources; quality assurance; facilities
and equipment; control of components,
in-process materials, and finished
products; production and process
controls; laboratory controls; acceptance
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]]>Agencies
[Federal Register Volume 78, Number 54 (Wednesday, March 20, 2013)]
[Notices]
[Pages 17214-17215]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-06390]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; Chronic Disease Self-Management Education Program
Standardized Data Collection
AGENCY: Administration on Aging (AoA), Administration for Community
Living (ACL), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration on Aging (AoA), now part of the
Administration for Community Living, is announcing that the proposed
collection of information listed below has been submitted to the Office
of Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Submit written comments on the collection of information by
April 19, 2013.
ADDRESSES: OIRA_submission@omb.eop.gov or by fax to 202.395.5806.
Attn: OMB Desk Officer for ACL, Office of Information and Regulatory
Affairs, OMB.
FOR FURTHER INFORMATION CONTACT: Michele Boutaugh, 404-987-3411 or
Michele.boutaugh@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, the
Administration on Aging (now part of the Administration for Community
[[Page 17215]]
Living) has submitted the following proposed collection of information
to OMB for review and clearance.
The ``Empowering Older Adults and Adults with Disabilities through
Chronic Disease Self-Management Education (CDSME) Programs''
cooperative agreement program is financed through 2012 Prevention and
Public Health Funds. The proposed data collection is necessary for
monitoring grant program operations and outcomes. AoA proposes to
gather information to monitor grantee progress, record location of
sites where workshops are held which will allow mapping of the delivery
infrastructure, and document participant attendance and demographic and
health characteristics. The proposed Participant Survey requests the
participants' gender, zip code and birthdate to allow for potential
Medicare claims matching and an analysis of changes in health care
utilization post participation.
In response to the 60-day Federal Register notice related to this
proposed data collection and published on July 23, 2013, four sets of
comments were received. Concern was expressed about the collection of
sensitive personal information. Most of the remaining comments provided
suggestions for enhancing the quality and clarity of the information to
be collected. The comments resulted in some revisions to the proposed
data collection tools. The originally proposed data collection tools,
the comments with responses and a revised set of data collection tools
may be found on the AoA Web site at: https://www.aoa.gov/AoARoot/AoA_Programs/Tools_Resources/collection_tools.aspx.
ACL estimates the burden of this collection of information as 440
hours for State Governments, 1050 hours for local agency staff, and
2,500 hours for individuals--Total burden is 3,990 hours per year.
Dated: March 15, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2013-06390 Filed 3-19-13; 8:45 am]
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