Submission for OMB Review; State Temporary Assistance for Needy Families Case Studies (New Collection), 33948-33949 [2019-15092]
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33948
Federal Register / Vol. 84, No. 136 / Tuesday, July 16, 2019 / Notices
TOTAL BURDEN ESTIMATES—Continued
[TANF, CW, Third Domain]
Previously
approved
respondents
for TANF
& CW
Instrument
Client interviews/focus groups .............................................
Client survey ........................................................................
Staff Survey .........................................................................
Total
number of
respondents
(TANF, CW,
EHS/HS)
48
600
120
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
with 3rd
domain
348
840
144
1
1
1
1
.25
.25
348
210
36
96
756
696
10,800
600
1
1
1
1
1
1
1
1
.25
.25
96
756
696
2,700
150
Evaluation
Administrator interviews/focus groups .................................
Staff interviews/focus groups ...............................................
Client interviews/focus groups .............................................
Client survey ........................................................................
Staff Survey .........................................................................
Estimated Total Burden Hours: 5,418.
Authority: 42 U.S.C. 1310.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019–15082 Filed 7–15–19; 8:45 am]
BILLING CODE 4184–07–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review; State
Temporary Assistance for Needy
Families Case Studies (New Collection)
Office of Planning, Research,
and Evaluation; Administration for
Children and Families; HHS.
ACTION: Request for public comment.
AGENCY:
The Office of Planning,
Research, and Evaluation (OPRE) is
proposing a data collection activity as
part of the State Temporary Assistance
for Needy Families (TANF) Case Studies
project. This study seeks to document
innovative employment and training
programs for low-income individuals
including TANF recipients and examine
the ways the programs provide or link
families to wraparound services. Over a
three-year period, the study will
conduct up to 12 comprehensive
qualitative case studies and up to 20
profiles of innovative programs to
showcase promising approaches.
DATES: Comments due within 30 days of
publication. OMB is required to make a
decision concerning the collection of
information between 30 and 60 days
after publication of this document in the
jspears on DSK30JT082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:33 Jul 15, 2019
Jkt 247001
48
96
96
6,000
120
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
directly to the following: Office of
Management and Budget, Paperwork
Reduction Project, Email: OIRA_
SUBMISSION@OMB.EOP.GOV. Attn:
Desk Officer for the Administration for
Children and Families.
Copies of the proposed collection may
be obtained by emailing
OPREinfocollection@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 State TANF Case
Studies project will involve several
phases including: (1) Identifying
innovative programs through a scan of
the field and engagement with
stakeholders; (2) visiting up to 12
selected programs to collect detailed
information and produce
comprehensive case studies of these
programs to enhance policymakers’ and
other stakeholders’ understanding of
promising programs helping lowincome individuals to succeed in the
labor force; and (3) gathering
information through telephone
interviews to produce up to 20 shorter
case studies. The proposed information
collection activities are: (1) Semi-
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
structured interviews with program and
partner administrators and frontline
staff; (2) in-depth interviews with
participants to better inform and
enhance understanding of client
experiences and perspectives; (3) a
guided case review with frontline staff
to capture information about client
characteristics as well as intensity,
frequency, duration, and sequencing of
services; and (4) an observation of
program services, such as case
management sessions, intakes and
referrals, services delivered in a
classroom setting, and work sites. The
study will take place over a three year
period.
Respondents: Respondents include
program administrators, frontline
program staff, and program participants.
Program administrators include staff
who administer and supervise the case
study program under review, TANF and
employment and training programs;
child care and other wraparound
supports; and other workforce programs
and partners such as community
colleges, adult basic education
providers, and employers; and state
decision makers, as appropriate.
Frontline program staff include intake
workers, case managers, job developers,
and other direct service providers who
work at TANF agencies and American
Job Centers, employment and training
providers such as community colleges,
and providers of wraparound supports,
such as child care subsidy frontline
staff. TANF and other low-income
program participants will also be
respondents. All participants will be
able to opt out of participating in the
data collection activities.
E:\FR\FM\16JYN1.SGM
16JYN1
33949
Federal Register / Vol. 84, No. 136 / Tuesday, July 16, 2019 / Notices
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
Instrument
Semi-structured program staff interview guide ....................
In-depth participant interview guide .....................................
Case review guide ...............................................................
Estimated Total Annual Burden
Hours: 91.
[FR Doc. 2019–15092 Filed 7–15–19; 8:45 am]
BILLING CODE 4184–09–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2014–N–1006]
Providing Regulatory Submissions in
Electronic Format—Certain Human
Pharmaceutical Product Applications
and Related Submissions Using the
Electronic Common Technical
Document Specifications (Revision 7);
Draft Guidance for Industry;
Availability
Food and Drug Administration,
HHS.
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry entitled
‘‘Providing Regulatory Submissions in
Electronic Format—Certain Human
Pharmaceutical Product Applications
and Related Submissions Using the
eCTD Specifications (Revision 7).’’ FDA
has identified certain submission types
that FDA believes warrant an exemption
(Type III drug master files (DMFs)) or a
long-term waiver (certain positron
emission tomography (PET) drug
products and certain Type II DMFs
supporting PET drugs or noncommercial
submissions or applications) from the
requirement to submit to the Agency in
eCTD format. In addition, this guidance
outlines certain circumstances where
FDA may determine that a short-term
waiver from electronic common
technical document (eCTD) submission
requirements could be granted. This
guidance is a revision of the final
guidance issued on January 29, 2019,
and when finalized, will supersede that
guidance.
jspears on DSK30JT082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:33 Jul 15, 2019
Jkt 247001
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
67
8
8
Submit either electronic or
written comments on the draft guidance
by September 16, 2019 to ensure that
the Agency considers your comment on
this draft guidance before it begins work
on the final version of the guidance.
ADDRESSES: You may submit comments
on any guidance at any time as follows:
Mary B. Jones,
ACF/OPRE Certifying Officer.
ACTION:
200
24
24
DATES:
Authority: Sec. 413, Pub. L. 115–31.
AGENCY:
Annual
number of
respondents
1
1
2
Average
burden
hours per
response
1
1.5
.75
Annual
burden
hours
67
12
12
2014–N–1006 for ‘‘Providing Regulatory
Submissions in Electronic Format—
Certain Human Pharmaceutical Product
Applications and Related Submissions
Using the eCTD Specifications (Revision
7).’’ Received comments will be placed
in the docket and, except for those
submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://www.gpo.gov/
fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
E:\FR\FM\16JYN1.SGM
16JYN1
Agencies
[Federal Register Volume 84, Number 136 (Tuesday, July 16, 2019)]
[Notices]
[Pages 33948-33949]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-15092]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; State Temporary Assistance for Needy
Families Case Studies (New Collection)
AGENCY: Office of Planning, Research, and Evaluation; Administration
for Children and Families; HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Office of Planning, Research, and Evaluation (OPRE) is
proposing a data collection activity as part of the State Temporary
Assistance for Needy Families (TANF) Case Studies project. This study
seeks to document innovative employment and training programs for low-
income individuals including TANF recipients and examine the ways the
programs provide or link families to wraparound services. Over a three-
year period, the study will conduct up to 12 comprehensive qualitative
case studies and up to 20 profiles of innovative programs to showcase
promising approaches.
DATES: Comments due within 30 days of publication. 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.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent directly to the following: Office
of Management and Budget, Paperwork Reduction Project, Email:
[email protected]. Attn: Desk Officer for the Administration
for Children and Families.
Copies of the proposed collection may be obtained 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 State TANF Case Studies project will involve
several phases including: (1) Identifying innovative programs through a
scan of the field and engagement with stakeholders; (2) visiting up to
12 selected programs to collect detailed information and produce
comprehensive case studies of these programs to enhance policymakers'
and other stakeholders' understanding of promising programs helping
low-income individuals to succeed in the labor force; and (3) gathering
information through telephone interviews to produce up to 20 shorter
case studies. The proposed information collection activities are: (1)
Semi-structured interviews with program and partner administrators and
frontline staff; (2) in-depth interviews with participants to better
inform and enhance understanding of client experiences and
perspectives; (3) a guided case review with frontline staff to capture
information about client characteristics as well as intensity,
frequency, duration, and sequencing of services; and (4) an observation
of program services, such as case management sessions, intakes and
referrals, services delivered in a classroom setting, and work sites.
The study will take place over a three year period.
Respondents: Respondents include program administrators, frontline
program staff, and program participants. Program administrators include
staff who administer and supervise the case study program under review,
TANF and employment and training programs; child care and other
wraparound supports; and other workforce programs and partners such as
community colleges, adult basic education providers, and employers; and
state decision makers, as appropriate. Frontline program staff include
intake workers, case managers, job developers, and other direct service
providers who work at TANF agencies and American Job Centers,
employment and training providers such as community colleges, and
providers of wraparound supports, such as child care subsidy frontline
staff. TANF and other low-income program participants will also be
respondents. All participants will be able to opt out of participating
in the data collection activities.
[[Page 33949]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total number Annual number Number of Average
Instrument of of responses per burden hours Annual burden
respondents respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
Semi-structured program staff 200 67 1 1 67
interview guide................
In-depth participant interview 24 8 1 1.5 12
guide..........................
Case review guide............... 24 8 2 .75 12
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 91.
Authority: Sec. 413, Pub. L. 115-31.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019-15092 Filed 7-15-19; 8:45 am]
BILLING CODE 4184-09-P