Agency Information Collection Activities; Proposed Collection; Comment Request; the National Maltreatment Reporting System, 15309-15310 [2016-06342]
Download as PDF
15309
Federal Register / Vol. 81, No. 55 / Tuesday, March 22, 2016 / Notices
Prevention and the Agency for Toxic
Substances and Disease Registry.
Claudette Grant,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2016–06348 Filed 3–21–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection;
Comment Request; the National
Maltreatment Reporting System
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) 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 requirements
relating to the National Maltreatment
Reporting System (NAMRS). The
proposed collection of information tools
may be found in the NAMRS section of
the ACL Web site.
DATES: Submit written or electronic
comments on the collection of
information by: May 23, 2016.
ADDRESSES: Submit electronic
comments on the collection of
information to Stephanie Whittier
Eliason at stephanie.whittiereliason@
acl.hhs.gov.
Submit written comments on the
collection of information to:
Administration for Community Living,
Attention: Stephanie Whittier Eliason,
330 C St SW., Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT:
Stephanie Whittier Eliason at
202.795.7467.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
asabaliauskas on DSK3SPTVN1PROD with NOTICES
SUMMARY:
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 request
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, ACL is publishing notice
of the proposed collection of
information set forth in this document.
Authority
This data collection effort is in
response to the Elder Justice Act of
2009, which amended title XX of the
Social Security Act (42.U.S.C. 13976 et
seq.). These provisions require that the
Secretary of HHS ‘‘collects and
disseminates data annually relating to
the abuse, exploitation, and neglect of
elders in coordination with the
Department of Justice’’ (Sec.
2041(a)(1)(B)), and ‘‘conducts research
related to the provision of adult
protective services’’ (Sec. 2041(a)(1)(D)).
Furthermore, the Elder Justice
Coordinating Council (EJCC) included
as its third recommendation for
increasing federal involvement in
addressing elder abuse, neglect, and
exploitation: Develop a national adult
protective services (APS) system based
upon standardized data collection and a
core set of service provision standards
and best practices.
Background
From 2013–2015, ACL, in partnership
with the U.S. Department of Health &
Human Services’ Office of the Assistant
Secretary for Planning and Evaluation
(ASPE), developed and pilot tested
NAMRS. When implemented, NAMRS
will be the first comprehensive, national
reporting system for APS programs.
NAMRS is intended to collect
quantitative and qualitative data on the
practices and policies of adult
protective services (APS) agencies, as
well as the outcomes of investigations
Number of
respondents
Instrument
Agency Component .........................................................................................
Key Indicators Component ..............................................................................
VerDate Sep<11>2014
17:34 Mar 21, 2016
Jkt 238001
PO 00000
Frm 00090
Fmt 4703
Sfmt 4703
into the maltreatment of older adults
and adults with disabilities.
In developing NAMRS, ACL and
ASPE convened key stakeholders to
identify data elements that are the most
critical for a national system. More than
40 state administrators, researchers,
service providers, and other
stakeholders provided input in focus
group conference calls. Additionally,
more than 30 state representatives from
25 different states met in three in-person
working sessions to discuss the uses of
collected data and the key
functionalities.
A pilot version of NAMRS was tested
in nine (9) diverse states, and refined
based on feedback from the pilot and
additional stakeholder engagement. A
full discussion on the background of
NAMRS, including the development of
the system, the public engagement
process, and the pilot testing can be
found in the NAMRS section of the ACL
Web site.
Proposed Collection Effort
NAMRS has been developed as a
voluntary system to collect annually
both summary and de-identified caselevel data on APS investigations.
NAMRS consists of three components:
(1) ACL proposes to collect
descriptive data on state agency policies
and practices from all states through the
‘‘Agency Component,’’ and
(2) Case-level, non-identifiable data
on persons who receive an investigation
by APS in response to an allegation of
abuse, neglect, or exploitation through
the ‘‘Case Component.’’
(3) For states that are unable to submit
a case-level file through the ‘‘Case
Component,’’ a ‘‘Key Indicators
Component’’ will be available for them
to submit data on a smaller set of core
items.
ACL will provide technical assistance
to states to assist in the preparation of
their data submissions. Respondents
will be state APS agencies and APS
agencies in the District of Columbia,
Puerto Rico, Guam, Northern Marianas
Islands, Virgin Islands, and American
Samoa. No personally identifiable
information will be collected. ACL has
calculated the following burden
estimates (information on how the
estimates were calculated is available in
the NAMRS section of the ACL Web
site):
Number of
responses per
respondent
56
31
E:\FR\FM\22MRN1.SGM
1
1
22MRN1
Average
burden hours
per response
13
40
Total burden
hours
728
1,240
15310
Federal Register / Vol. 81, No. 55 / Tuesday, March 22, 2016 / Notices
Number of
responses per
respondent
Number of
respondents
Instrument
Average
burden hours
per response
Total burden
hours
Case Component .............................................................................................
25
1
150
3,750
Estimated Total Annual Burden Hours .....................................................
........................
........................
........................
5,718
With respect to the collection of
information via NAMRS, ACL
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. The
proposed collection of information tools
may be found in the NAMRS section of
the ACL Web site.
Dated: March 16, 2016.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
[FR Doc. 2016–06342 Filed 3–21–16; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2015–D–2104]
Assessment of RadiofrequencyInduced Heating in the Magnetic
Resonance Environment for MultiConfiguration Passive Medical
Devices; Guidance for Industry and
Food and Drug Administration Staff;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of the
guidance entitled ‘‘Assessment of
Radiofrequency-Induced Heating in the
Magnetic Resonance (MR) Environment
for Multi-Configuration Passive Medical
Devices.’’ FDA is confronted with an
increasing number of premarket
submissions that include an MR
asabaliauskas on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:34 Mar 21, 2016
Jkt 238001
Conditional labeling claim for
multiconfiguration passive medical
devices. The assessment of
radiofrequency (RF)-induced heating of
such devices, typically comprised of
many parts, strongly depends on the
specific device geometry and can
therefore lead to a prohibitively large
number of test cases. This guidance
provides an approach to reduce the
number of possible device
configurations to a manageable number,
and it provides guidance on how to
assess the RF-induced device heating for
an individual configuration.
DATES: Submit either electronic or
written comments on this guidance at
any time. General comments on Agency
guidance documents are welcome at any
time.
ADDRESSES: You may submit comments
as follows:
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): Division of
PO 00000
Frm 00091
Fmt 4703
Sfmt 4703
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Division of Dockets
Management, 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–
2015–D–2104 for ‘‘Assessment of
Radiofrequency-Induced Heating in the
Magnetic Resonance (MR) Environment
for Multi-Configuration Passive Medical
Devices.’’ 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
Division of Dockets Management
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 Division of Dockets
Management. 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.fda.gov/
E:\FR\FM\22MRN1.SGM
22MRN1
Agencies
[Federal Register Volume 81, Number 55 (Tuesday, March 22, 2016)]
[Notices]
[Pages 15309-15310]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-06342]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; the National Maltreatment Reporting System
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) 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
requirements relating to the National Maltreatment Reporting System
(NAMRS). The proposed collection of information tools may be found in
the NAMRS section of the ACL Web site.
DATES: Submit written or electronic comments on the collection of
information by: May 23, 2016.
ADDRESSES: Submit electronic comments on the collection of information
to Stephanie Whittier Eliason at stephanie.whittiereliason@acl.hhs.gov.
Submit written comments on the collection of information to:
Administration for Community Living, Attention: Stephanie Whittier
Eliason, 330 C St SW., Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT: Stephanie Whittier Eliason at
202.795.7467.
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 request 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, ACL is publishing notice of the proposed collection
of information set forth in this document.
Authority
This data collection effort is in response to the Elder Justice Act
of 2009, which amended title XX of the Social Security Act (42.U.S.C.
13976 et seq.). These provisions require that the Secretary of HHS
``collects and disseminates data annually relating to the abuse,
exploitation, and neglect of elders in coordination with the Department
of Justice'' (Sec. 2041(a)(1)(B)), and ``conducts research related to
the provision of adult protective services'' (Sec. 2041(a)(1)(D)).
Furthermore, the Elder Justice Coordinating Council (EJCC) included as
its third recommendation for increasing federal involvement in
addressing elder abuse, neglect, and exploitation: Develop a national
adult protective services (APS) system based upon standardized data
collection and a core set of service provision standards and best
practices.
Background
From 2013-2015, ACL, in partnership with the U.S. Department of
Health & Human Services' Office of the Assistant Secretary for Planning
and Evaluation (ASPE), developed and pilot tested NAMRS. When
implemented, NAMRS will be the first comprehensive, national reporting
system for APS programs. NAMRS is intended to collect quantitative and
qualitative data on the practices and policies of adult protective
services (APS) agencies, as well as the outcomes of investigations into
the maltreatment of older adults and adults with disabilities.
In developing NAMRS, ACL and ASPE convened key stakeholders to
identify data elements that are the most critical for a national
system. More than 40 state administrators, researchers, service
providers, and other stakeholders provided input in focus group
conference calls. Additionally, more than 30 state representatives from
25 different states met in three in-person working sessions to discuss
the uses of collected data and the key functionalities.
A pilot version of NAMRS was tested in nine (9) diverse states, and
refined based on feedback from the pilot and additional stakeholder
engagement. A full discussion on the background of NAMRS, including the
development of the system, the public engagement process, and the pilot
testing can be found in the NAMRS section of the ACL Web site.
Proposed Collection Effort
NAMRS has been developed as a voluntary system to collect annually
both summary and de-identified case-level data on APS investigations.
NAMRS consists of three components:
(1) ACL proposes to collect descriptive data on state agency
policies and practices from all states through the ``Agency
Component,'' and
(2) Case-level, non-identifiable data on persons who receive an
investigation by APS in response to an allegation of abuse, neglect, or
exploitation through the ``Case Component.''
(3) For states that are unable to submit a case-level file through
the ``Case Component,'' a ``Key Indicators Component'' will be
available for them to submit data on a smaller set of core items.
ACL will provide technical assistance to states to assist in the
preparation of their data submissions. Respondents will be state APS
agencies and APS agencies in the District of Columbia, Puerto Rico,
Guam, Northern Marianas Islands, Virgin Islands, and American Samoa. No
personally identifiable information will be collected. ACL has
calculated the following burden estimates (information on how the
estimates were calculated is available in the NAMRS section of the ACL
Web site):
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Agency Component................................ 56 1 13 728
Key Indicators Component........................ 31 1 40 1,240
[[Page 15310]]
Case Component.................................. 25 1 150 3,750
---------------
Estimated Total Annual Burden Hours......... .............. .............. .............. 5,718
----------------------------------------------------------------------------------------------------------------
With respect to the collection of information via NAMRS, ACL
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. The proposed collection of
information tools may be found in the NAMRS section of the ACL Web
site.
Dated: March 16, 2016.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2016-06342 Filed 3-21-16; 8:45 am]
BILLING CODE 4154-01-P