Agency Information Collection Activities; Proposed Collection; Comment Request; Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery, 57193-57194 [2015-24066]
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Federal Register / Vol. 80, No. 183 / Tuesday, September 22, 2015 / Notices
(19) Notice of Rights Handout and Notice
of Rights and Provision of Services: Care
providers are required to provide to all UC
under the Flores v. Reno Settlement
Agreement.
(20) Legal Service Provider List for UC: List
of organizations who offer free legal
representation and help for UC with State
and Federal courts, immigration hearings,
and appeals. Required under the Flores
Settlement Agreement.
(21) URM Application: Certain populations
of children and youth in ORR custody may
become eligible for the Unaccompanied
Refugee Minors Program, which is a State
administered foster care program. In such
instances the care provider facility or other
interested party may complete this
application form on behalf of the child.
(22) Withdrawal of Application or
Declination of Placement Form: If a youth
who has submitted an application for the
URM Program wishes to withdraw this
application, or if he or she has been offered
placement and wishes to decline this
placement, the youth must complete this
form.
(23) Standard Shelter Tour Request: Used
by members of the public and the media to
submit to care providers in order to tour a
shelter facility.
57193
Respondents
UC in ORR care and custody (they are
generally referred to ORR from the DHS)
and who are then referred to ORR’s
Network of Care Providers.
Staff in ORR’s Care Provider Network,
including those in shelter care, secure
and staff secure care, foster care, and
residential treatment centers.
Approved sponsors of UC released
from ORR care.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
tkelley on DSK3SPTVN1PROD with NOTICES
UC Portal Capacity Report .....................................................
Further Assessment Swift Track (FAST) Placement Tool .....
Placement Authorization Form ...............................................
Notice of Placement in Secure or Staff Secure Facility .........
Initial Intakes Form .................................................................
UC Assessment ......................................................................
Individual Service Plan ...........................................................
UC Case Review Form ...........................................................
New Sponsor Form .................................................................
Transfer Request and Tracking Form ....................................
Long Term Foster Care Placement Memo .............................
Travel Request Form for UC Long Term Foster Care ...........
Notice of Transfer to ICE Chief Counsel and Change of Address.
Care Provider Release Checklist ............................................
Release Request ....................................................................
Discharge Notification .............................................................
Verification of Release ............................................................
Child Advocate Referral and Appointment Form ....................
Notice of Rights Handout and Notice of Rights and Provision of Services.
Legal Service Provider List for UC .........................................
URM Application .....................................................................
Withdrawal of Application or Declination of Placement Form
Standard Shelter Tour Request ..............................................
Estimated Total Annual Burden
Hours: 172,636.
In compliance with the requirements
of Section 506(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: infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
VerDate Sep<11>2014
17:39 Sep 21, 2015
Jkt 235001
Number of
responses
per
respondent
Average burden hours per
response
50
2,320
58,000
2,320
58,000
58,000
58,000
58,000
55,200
1,000
279
20
2,320
1
1
1
1
1
1
1
1
1
1
1
1
1
.16/hour ......................................
.25/hour ......................................
.1/hour ........................................
.1/hour ........................................
.25/hour ......................................
.50/hour ......................................
.25 ..............................................
.50/hour ......................................
.25/hour ......................................
.25/hour ......................................
.1/hour ........................................
.25/hour ......................................
.1/hour ........................................
8
580
5,800
232
14,500
29,000
14,500
29,000
13,800
250
28
5
232
55,200
55,200
716
55,200
250
58,000
1
3
1
1
1
1
.1 ................................................
.25 hour ......................................
.25/hour ......................................
.1/hour ........................................
.50 ..............................................
.1/hour ........................................
5,520
41,400
179
5,520
125
5,800
58,000
350
10
60
1
1
1
1
.1 ................................................
1 .................................................
.1/hour ........................................
.1/hour ........................................
5,800
350
1
6
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
PO 00000
Total burden
hours
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2015–23978 Filed 9–21–15; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Generic Clearance
for the Collection of Qualitative
Feedback on Agency Service Delivery
Administration for Community
Living, HHS.
AGENCY:
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57194
Federal Register / Vol. 80, No. 183 / Tuesday, September 22, 2015 / Notices
60-Day notice of submission of
information collection approval from
the Office of Management and Budget
and request for comments.
ACTION:
As part of a Federal
Government-wide effort to streamline
the process to seek feedback from the
public on service delivery, the
Administration for Community Living
proposes to submitted a Generic
Information Collection Request (Generic
ICR): ‘‘Generic Clearance for the
Collection of Qualitative Feedback on
Agency Service Delivery’’ to OMB for
approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et.
seq.).
DATES: Submit written or electronic
comments on the collection of
information by November 23, 2015.
ADDRESSES: Submit electronic
comments on the collection of
information to: Susan Jenkins at
Susan.Jenkins@aoa.hhs.gov.
Submit written comments on the
collection of information to
Administration for Community Living,
Washington, DC 20201, Attn. Susan
Jenkins.
FOR FURTHER INFORMATION CONTACT:
Susan Jenkins at 202.357.3591.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Title:
Generic Clearance for the Collection of
Qualitative Feedback on Agency Service
Delivery.
Abstract: The information collection
activity will garner qualitative customer
and stakeholder feedback in an efficient,
timely manner, in accordance with the
Administration’s commitment to
improving service delivery. By
qualitative feedback we mean
information that provides useful
insights on perceptions and opinions,
but are not statistical surveys that yield
quantitative results that can be
generalized to the population of study.
This feedback will provide insights into
customer or stakeholder perceptions,
experiences and expectations, provide
an early warning of issues with service,
or focus attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
Feedback collected under this generic
clearance will provide useful
information, but it will not yield data
that can be generalized to the overall
population. This type of generic
tkelley on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:39 Sep 21, 2015
Jkt 235001
clearance for qualitative information
will not be used for quantitative
information collections that are
designed to yield reliably actionable
results, such as monitoring trends over
time or documenting program
performance. Such data uses require
more rigorous designs that address: the
target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
sample size, the expected response rate,
methods for assessing potential nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior
fielding the study. Depending on the
degree of influence the results are likely
to have, such collections may still be
eligible for submission for other generic
mechanisms that are designed to yield
quantitative results.
Dated: September 17, 2015.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
[FR Doc. 2015–24066 Filed 9–21–15; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0114]
Agency Information Collection
Activities; Proposed Collection;
Submission for Office of Management
and Budget Review; Request for
Samples and Protocols
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
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 October 22,
2015.
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:
202–395–7285, or emailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
SUMMARY:
PO 00000
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Fmt 4703
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OMB control number 0910–0206. Also
include the FDA docket number found
in brackets in the heading of this
document.
FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002,
PRAStaff@fda.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
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 21 CFR 610.2, the Center for
Biologics Evaluation and Research
(CBER) or the Center for Drugs
Evaluation and Research may at any
time require manufacturers of licensed
biological products to submit to FDA
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:
21 CFR 660.6 (Antibody to Hepatitis B
Surface Antigen); 21 CFR 660.36
(Reagent Red Blood Cells); and 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
E:\FR\FM\22SEN1.SGM
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]]>Agencies
[Federal Register Volume 80, Number 183 (Tuesday, September 22, 2015)]
[Notices]
[Pages 57193-57194]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-24066]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; Generic Clearance for the Collection of Qualitative
Feedback on Agency Service Delivery
AGENCY: Administration for Community Living, HHS.
[[Page 57194]]
ACTION: 60-Day notice of submission of information collection approval
from the Office of Management and Budget and request for comments.
-----------------------------------------------------------------------
SUMMARY: As part of a Federal Government-wide effort to streamline the
process to seek feedback from the public on service delivery, the
Administration for Community Living proposes to submitted a Generic
Information Collection Request (Generic ICR): ``Generic Clearance for
the Collection of Qualitative Feedback on Agency Service Delivery'' to
OMB for approval under the Paperwork Reduction Act (PRA) (44 U.S.C.
3501 et. seq.).
DATES: Submit written or electronic comments on the collection of
information by November 23, 2015.
ADDRESSES: Submit electronic comments on the collection of information
to: Susan Jenkins at Susan.Jenkins@aoa.hhs.gov.
Submit written comments on the collection of information to
Administration for Community Living, Washington, DC 20201, Attn. Susan
Jenkins.
FOR FURTHER INFORMATION CONTACT: Susan Jenkins at 202.357.3591.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Title:
Generic Clearance for the Collection of Qualitative Feedback on Agency
Service Delivery.
Abstract: The information collection activity will garner
qualitative customer and stakeholder feedback in an efficient, timely
manner, in accordance with the Administration's commitment to improving
service delivery. By qualitative feedback we mean information that
provides useful insights on perceptions and opinions, but are not
statistical surveys that yield quantitative results that can be
generalized to the population of study. This feedback will provide
insights into customer or stakeholder perceptions, experiences and
expectations, provide an early warning of issues with service, or focus
attention on areas where communication, training or changes in
operations might improve delivery of products or services. These
collections will allow for ongoing, collaborative and actionable
communications between the Agency and its customers and stakeholders.
It will also allow feedback to contribute directly to the improvement
of program management.
Feedback collected under this generic clearance will provide useful
information, but it will not yield data that can be generalized to the
overall population. This type of generic clearance for qualitative
information will not be used for quantitative information collections
that are designed to yield reliably actionable results, such as
monitoring trends over time or documenting program performance. Such
data uses require more rigorous designs that address: the target
population to which generalizations will be made, the sampling frame,
the sample design (including stratification and clustering), the
precision requirements or power calculations that justify the proposed
sample size, the expected response rate, methods for assessing
potential non-response bias, the protocols for data collection, and any
testing procedures that were or will be undertaken prior fielding the
study. Depending on the degree of influence the results are likely to
have, such collections may still be eligible for submission for other
generic mechanisms that are designed to yield quantitative results.
Dated: September 17, 2015.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2015-24066 Filed 9-21-15; 8:45 am]
BILLING CODE 4154-01-P
