Proposed Information Collection Activity; Extension of Assets for Independence (AFI) Performance Progress Report (PPR) (OMB #0970-0483), 24156-24157 [2019-10863]
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Federal Register / Vol. 84, No. 101 / Friday, May 24, 2019 / Notices
receiving access to the Medicare
eligibility information for the purpose of
conducting real-time 270/271 inquiry/
response transactions. Form Number:
CMS–10157 (OMB control number:
0938–0960); Frequency: Yearly; Affected
Public: Private Sector; Business or other
for profits, Not-for-Profits Institutions;
Number of Respondents: 1000; Total
Annual Responses: 1000; Total Annual
Hours: 250. (For policy questions
regarding this collection contact
Rupinder Singh at 410 786–7484.)
Dated: May 21, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
Statutory Authority: Social Security Act,
Title XI, Section 1110, 42 U.S.C. 1310.
Elizabeth Leo,
Senior Grants Policy Specialist, Division of
Grants Policy, Office of Administration.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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Administration for Children and
Families
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Proposed Information Collection
Activity; Extension of Assets for
Independence (AFI) Performance
Progress Report (PPR) (OMB #0970–
0483)
Administration for Children and
Families
[CFDA Number: 93.647]
Announcement of an Unsolicited
Single-Source Grant Award to the
Woodson Center in Washington, DC
Office of Community Services;
Administration for Children and
Families; HHS.
ACTION: Request for public comment.
AGENCY:
Office of Planning, Research
and Evaluation, Administration for
Children and Families, Department of
Health and Human Services.
ACTION: Notice of issuance.
AGENCY:
The Office of Community
Services (OCS), Administration for
Children and Families (ACF) is
requesting approval of a three-year
extension of the Assets for
Independence (AFI) Performance
Progress Report (PPR) Long Form and
AFI PPR Short Form (OMB #0970–0483,
expiration 8/31/2019). There are no
changes requested to the forms.
DATES: Comments due within 60 days of
publication. 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.
ADDRESSES: Copies of the proposed
collection of information can be
SUMMARY:
The Administration for
Children and Families (ACF), Office of
Planning, Research and Evaluation
announces the award of a grant in the
amount of $150,000 to the Woodson
Center of Washington, DC, to support an
environmental scan of models of service
for privately managed foster care.
DATES: The project period will be May
15, 2019, to November 14, 2019.
FOR FURTHER INFORMATION CONTACT:
Wendy DeCourcey, Senior Social
Science Analyst; Office of Planning,
Research and Evaluation; 330 C Street
SW, Washington, DC 20201. Telephone:
202–260–2039.
SUMMARY:
The
Woodson Center plans to complete an
environmental scan of privately
managed foster care systems in multiple
states. This environmental scan is
expected to inform future networking
efforts among similar organizations and
identification and dissemination of best
practices.
SUPPLEMENTARY INFORMATION:
obtained and comments may be
forwarded by emailing infocollection@
acf.hhs.gov. Alternatively, copies can
also be obtained by writing to the
Administration for Children and
Families, Office of Planning, Research,
and Evaluation, 330 C Street SW,
Washington, DC 20201, Attn: OPRE
Reports Clearance Officer. All requests,
emailed or written, should be identified
by the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: The Assets for
Independence (AFI) Act (Title IV of the
Community Opportunities,
Accountability, and Training and
Educational Services Act of 1998, Pub.
L. 105–285, [42 U.S.C. 604 note])
requires that organizations operating
AFI projects submit annual progress
reports.
This request is for approval and
extension of the current AFI PPR that
expires August 31, 2019. OCS will
continue to use the data collected in the
AFI PPR to prepare the annual AFI
Report to Congress, to evaluate and
monitor the performance of the AFI
program overall and of individual
projects, and to inform and support
technical assistance efforts. The AFI
PPR will continue to fulfill AFI Act
reporting requirements and program
purposes.
AFI program grantees are required to
submit Standard Form Performance
Progress Reports (SF–PPR)
semiannually: One time per year using
an abbreviated short form and one time
using a long form. Both data collection
instruments are available for review
online at: https://www.acf.hhs.gov/ocs/
resource/afi-ppr-long-form, https://
www.acf.hhs.gov/ocs/resource/afi-pprshort-form.
Note: This request does not affect
financial reporting requirements for AFI
grantees. The SF–425 will still be
required semiannually throughout the
grant project period with a final report
due 90 days after the grant project
period ends.
Respondents: Assets for
Independence (AFI) program grantees.
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
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Instrument
AFI PPR Short Form .......................................................................................
AFI PPR Long Form ........................................................................................
Estimated Total Annual Burden
Hours: 623.5.
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145
145
Comments: The Department
specifically requests comments on (a)
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Annual
number of
responses per
respondent
1
1
Average
burden hours
per response
0.5
3.8
Annual
burden hours
72.5
551
whether the proposed collection of
information is necessary for the proper
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Federal Register / Vol. 84, No. 101 / Friday, May 24, 2019 / Notices
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.
Authority: Pub. L. 105–285, [42 U.S.C. 604
note].
Mary B. Jones,
ACF/OPRE Certifying Officer.
column, in the DATES section, the
sentence ‘‘The meeting will be held on
May 30, 2019, from 10 a.m. to 4 p.m.
and on May 31, 2019, from 8 a.m. to 4
p.m.’’ is changed to read as follows:
The meeting will be held on May 30,
2019, from 9 a.m. to 4 p.m. and on May
31, 2019, from 8 a.m. to 4 p.m.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14,
relating to the advisory committees.
Dated: May 21, 2019.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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Food and Drug Administration
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Docket No. FDA–2019–N–2037]
Electronic Nicotine Delivery System
Device and E-Liquid Manufacturer Site
Tours Program
Food and Drug Administration
[Docket No. FDA–2019–N–1281]
General and Plastic Surgery Devices
Panel of the Medical Devices Advisory
Committee; Amendment of Notice
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing an
amendment to the notice of meeting of
the General and Plastic Surgery Devices
Panel of the Medical Devices Advisory
Committee. This meeting was
announced in the Federal Register of
April 24, 2019. The amendment is being
made to reflect a change in the DATES
portion of the document. There are no
other changes.
FOR FURTHER INFORMATION CONTACT:
Patricio Garcia, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. G610, Silver Spring,
MD 20993, 301–796–6875,
Patricio.garcia@fda.hhs.gov; or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area). Please call the
Information Line for up-to-date
information on this meeting.
SUPPLEMENTARY INFORMATION: In the
Federal Register of April 24, 2019 (84
FR 17173), FDA announced that a
meeting of the General and Plastic
Surgery Devices Panel of the Medical
Devices Advisory Committee would be
held on May 30, 2019, from 10 a.m. to
4 p.m. On page 17173, in the third
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SUMMARY:
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AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA), Center for
Tobacco Products (CTP), is announcing
an invitation for participation in its
voluntary Electronic Nicotine Delivery
System (ENDS) Device and E-Liquid
Manufacturer Site Tours Program. This
program is intended to give CTP staff an
opportunity to visit facilities that
develop, manufacture, or test ENDS
devices or e-liquids (including pods or
cartridges) to gain a better
understanding of the processes involved
in the development, manufacturing, and
testing of ENDS devices and e-liquids.
The site tours in this program are not
intended as regulatory inspections. The
purpose of this document is to invite
ENDS device or e-liquid manufacturers
that can demonstrate assembly process
and present supply chain information,
and laboratories that conduct ENDS
aerosol and e-liquid testing, that are
interested in participating in the ENDS
Device and E-Liquid Manufacturer Site
Tours Program to submit requests to
CTP.
DATES: Submit either an electronic or
written request for participation in this
program by July 23, 2019. See section IV
of this document for information on
requests for participation.
ADDRESSES: If your facility is interested
in participating in a facility visit, please
submit a request either electronically to
SUMMARY:
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24157
https://www.regulations.gov or in
writing to the Dockets Management Staff
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Karla Price, Office of Science, Center for
Tobacco Products, Food and Drug
Administration, Document Control
Center, 10903 New Hampshire Ave.,
Bldg. 71, Rm. G335, Silver Spring, MD
20993–0002, 1–877–287–1373, email:
AskCTP@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On June 22, 2009, the Family
Smoking Prevention and Tobacco
Control Act (Pub. L. 111–31) (Tobacco
Control Act) was signed into law,
amending the Federal Food, Drug, and
Cosmetic Act (FD&C Act) by, among
other things, adding a new chapter
(chapter IX) granting FDA the authority
to regulate tobacco product
manufacturing, distribution, and
marketing. The Tobacco Control Act
provides FDA authority to regulate
cigarettes, cigarette tobacco, roll-yourown tobacco, smokeless tobacco, and
any other tobacco products that the
Agency by regulation deems to be
subject to the law.
On May 10, 2016, FDA published a
final rule entitled ‘‘Deeming Tobacco
Products To Be Subject to the Federal
Food, Drug, and Cosmetic Act, as
Amended by the Family Smoking
Prevention and Tobacco Control Act;
Restrictions on the Sale and Distribution
of Tobacco Products and Required
Warning Statements for Tobacco
Products’’ (81 FR 28974), which became
effective on August 8, 2016. Under this
rule, all products, such as ENDS, that
meet the statutory definition of ‘‘tobacco
product’’ set forth in section 201(rr) of
the FD&C Act (21 U.S.C. 321(rr)),
including components and parts, but
excluding accessories of newly deemed
products, are now subject to chapter IX
of the FD&C Act.
CTP’s Office of Science is conducting
the ENDS Device and E-Liquid
Manufacturer Site Tours Program to
provide its staff an opportunity to visit
facilities that develop, manufacture, or
test ENDS devices or e-liquids
(including pods or cartridges). The
ENDS device and e-liquid facilities are
regulated by FDA if they, among other
things, manufacture products that meet
the statutory definition of a ‘‘tobacco
product’’ set forth in section 201(rr) of
the FD&C Act. The site tours will aid the
Agency in gaining a better
understanding of the processes involved
in developing, manufacturing, and
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]]>Agencies
[Federal Register Volume 84, Number 101 (Friday, May 24, 2019)]
[Notices]
[Pages 24156-24157]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-10863]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Extension of Assets for
Independence (AFI) Performance Progress Report (PPR) (OMB #0970-0483)
AGENCY: Office of Community Services; Administration for Children and
Families; HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Office of Community Services (OCS), Administration for
Children and Families (ACF) is requesting approval of a three-year
extension of the Assets for Independence (AFI) Performance Progress
Report (PPR) Long Form and AFI PPR Short Form (OMB #0970-0483,
expiration 8/31/2019). There are no changes requested to the forms.
DATES: Comments due within 60 days of publication. 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.
ADDRESSES: Copies of the proposed collection of information can be
obtained and comments may be forwarded by emailing
[email protected]. Alternatively, copies can also be obtained
by writing to the Administration for Children and Families, Office of
Planning, Research, and Evaluation, 330 C Street SW, Washington, DC
20201, Attn: OPRE Reports Clearance Officer. All requests, emailed or
written, should be identified by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: The Assets for Independence (AFI) Act (Title IV of the
Community Opportunities, Accountability, and Training and Educational
Services Act of 1998, Pub. L. 105-285, [42 U.S.C. 604 note]) requires
that organizations operating AFI projects submit annual progress
reports.
This request is for approval and extension of the current AFI PPR
that expires August 31, 2019. OCS will continue to use the data
collected in the AFI PPR to prepare the annual AFI Report to Congress,
to evaluate and monitor the performance of the AFI program overall and
of individual projects, and to inform and support technical assistance
efforts. The AFI PPR will continue to fulfill AFI Act reporting
requirements and program purposes.
AFI program grantees are required to submit Standard Form
Performance Progress Reports (SF-PPR) semiannually: One time per year
using an abbreviated short form and one time using a long form. Both
data collection instruments are available for review online at: https://www.acf.hhs.gov/ocs/resource/afi-ppr-long-form, https://www.acf.hhs.gov/ocs/resource/afi-ppr-short-form.
Note: This request does not affect financial reporting requirements
for AFI grantees. The SF-425 will still be required semiannually
throughout the grant project period with a final report due 90 days
after the grant project period ends.
Respondents: Assets for Independence (AFI) program grantees.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Annual number Average burden
Instrument Total number of responses hours per Annual burden
of respondents per respondent response hours
----------------------------------------------------------------------------------------------------------------
AFI PPR Short Form.............................. 145 1 0.5 72.5
AFI PPR Long Form............................... 145 1 3.8 551
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 623.5.
Comments: The Department specifically requests comments on (a)
whether the proposed collection of information is necessary for the
proper
[[Page 24157]]
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.
Authority: Pub. L. 105-285, [42 U.S.C. 604 note].
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019-10863 Filed 5-23-19; 8:45 am]
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