Agency Information Collection Activities: Proposed Collection; Comment Request, 22835-22836 [2017-10085]
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Federal Register / Vol. 82, No. 95 / Thursday, May 18, 2017 / Notices
22835
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
Number of
respondents
Number of
responses per
respondent
Avgerage
burden per
response
(in hours)
...........................................................
........................
........................
........................
Type of respondents
Total ...........................................
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2017–10090 Filed 5–17–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10506]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. 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 or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
July 17, 2017.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
jstallworth on DSK7TPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
13:43 May 17, 2017
Jkt 241001
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10506 Conditions of
Participation for Community Mental
Health Centers and Supporting
Regulations
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.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
Total burden
(in hours)
225
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
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Conditions of
Participation for Community Mental
Health Centers and Supporting
Regulations; Use: On June 17, 2011, we
proposed for the first time new
conditions of participation (CoPs) for
community mental health centers
(CMHCs). We finalized it in the final
rule that published October 29, 2013 (78
FR 64604), with an effective date 12months after publication of the final
rule. These CoPs which are based on
criteria prescribed in law and are
standards designed to ensure that each
facility has properly trained staff to
provide the appropriate safe physical
environment for patients. These
particular standards reflect comparable
standards developed by industry
organizations such as the Joint
Commission. The primary users of this
information will be State agency
surveyors, CMS and CMHCs for the
purpose of ensuring compliance with
Medicare CoPs as well as ensuring the
quality of care provided by CMHCs to
patients. Form Number: CMS–10506
(OMB Control number: 0938–1245);
Frequency: Occasionally; Affected
Public: Private sector—Business or other
for-profits and Not-for-profit
organizations; Number of Respondents:
68; Total Annual Responses: 18,586;
Total Annual Hours: 2,091. (For policy
questions regarding this collection
contact Mary Rossi-Coajou at 410–786–
6051.)
E:\FR\FM\18MYN1.SGM
18MYN1
22836
Federal Register / Vol. 82, No. 95 / Thursday, May 18, 2017 / Notices
Dated: May 15, 2017.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2017–10085 Filed 5–17–17; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: Scientific
Registry of Transplant Recipients
Information Collection Effort for
Potential Donors for Living Organ
Donation—New
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services (HHS).
AGENCY:
ACTION:
To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call the HRSA Information Collection
Clearance Officer at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference, pursuant to Section
3506(c)(2)(A), the Paperwork Reduction
Act of 1995.
Information Collection Request Title:
Scientific Registry of Transplant
Recipients Information Collection Effort
for Potential Donors for Living Organ
Donation—New.
Abstract: The Scientific Registry of
Transplant Recipients (SRTR) is
administered under contract with
HRSA, an agency of HHS. HHS is
authorized to establish and maintain
mechanisms to evaluate the long-term
effects associated with living donations
(42 U.S.C. 273a) and is required to
submit to Congress an annual report on
the long-term health effects of living
donation (42 U.S.C. 273b). The SRTR
contractor will establish a pilot living
donor registry in which 14 transplant
programs will register all potential
living donors who provide informed
consent to participate in the pilot
registry. The SRTR’s authority to collect
information concerning potential living
donors is set forth in the Organ
Procurement and Transplantation
Network final rule requiring Organ
Procurement Organizations and
transplant hospitals to submit to the
SRTR, as appropriate, information
regarding ‘‘donors of organs’’ and ‘‘other
information that the Secretary deems
appropriate’’ 42 CFR 121.11(b)(2).
Need and Proposed Use of the
Information: The transplant programs
will submit health information collected
FOR FURTHER INFORMATION CONTACT:
Notice.
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects of the Paperwork Reduction Act
of 1995, HRSA announces plans to
submit an Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting the ICR to
OMB, HRSA seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
SUMMARY:
Comments on this ICR should be
received no later than July 17, 2017.
DATES:
Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N39, 5600 Fishers
Lane, Rockville, MD 20857.
ADDRESSES:
at the time of donation evaluation
through a secure web-based data
collection tool developed by the
contractor. The SRTR contractor will
maintain contact with registry
participants and collect data on longterm health outcomes through surveys.
The data collection will also include
outcomes of evaluation including
reasons for non-donation. The goal of
the pilot registry is to develop data
collection tools and survey instruments
that can be used to expand the registry
to include most, if not all, living donor
transplant programs in the United States
over time. Monitoring and reporting of
long-term health outcomes of living
donors post donation will provide
useful information to transplant
programs in their future donor selection
process and will aid potential living
donors in their decision to pursue living
donation.
Likely Respondents: Potential living
donors, transplant programs, medical
and scientific organizations, and public
organizations.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose, or provide the information
requested. This includes the time
needed to: (1) Review instructions;
develop, acquire, install, and utilize
technology and systems for the purpose
of collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; (2) train
personnel to respond to a request for
collection of information; (3) search data
sources; (4) complete and review the
collection of information; and (5) to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this Information
Collection Request are summarized in
the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Average
number of
responses per
respondent
Average
burden per
response
(in hours)
Total
number of
responses
Total
burden
hours
14
776
55
1
770
776
1
.50
770
388
Total ..............................................................................
jstallworth on DSK7TPTVN1PROD with NOTICES
Potential Living Donor Registration form .............................
Potential Living Donor Follow-up form ................................
* 790
........................
1,546
........................
1,158
* Number of respondents for potential living donor registration forms is based on the number of programs participating in the pilot registry.
Number of respondents for potential living donor follow-up forms is based on the number of potential living donors evaluated at the 14 participating programs in 2015.
HRSA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
VerDate Sep<11>2014
13:43 May 17, 2017
Jkt 241001
functions; (2) the accuracy of the
estimated burden; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4) the
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
use of automated collection techniques
or other forms of information
E:\FR\FM\18MYN1.SGM
18MYN1
Agencies
[Federal Register Volume 82, Number 95 (Thursday, May 18, 2017)]
[Notices]
[Pages 22835-22836]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-10085]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-10506]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. 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 or reinstatement of an
existing collection of information) and to allow 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our burden estimates or any other aspect of this
collection of information, including the necessity and utility of the
proposed information collection for the proper performance of the
agency's functions, the accuracy of the estimated burden, ways to
enhance the quality, utility, and clarity of the information to be
collected, and the use of automated collection techniques or other
forms of information technology to minimize the information collection
burden.
DATES: Comments must be received by July 17, 2017.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number. To be assured consideration, comments and
recommendations must be submitted in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) that are accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ___, Room C4-26-05, 7500 Security Boulevard, Baltimore,
Maryland 21244-1850.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS' Web site address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: Reports Clearance Office at (410) 786-
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-10506 Conditions of Participation for Community Mental Health
Centers and Supporting Regulations
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. The term
``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. Section 3506(c)(2)(A) of the PRA requires federal agencies
to publish a 60-day notice in the Federal Register concerning each
proposed collection of information, including each proposed extension
or reinstatement of an existing collection of information, before
submitting the collection to OMB for approval. To comply with this
requirement, CMS is publishing this notice.
Information Collection
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Conditions of
Participation for Community Mental Health Centers and Supporting
Regulations; Use: On June 17, 2011, we proposed for the first time new
conditions of participation (CoPs) for community mental health centers
(CMHCs). We finalized it in the final rule that published October 29,
2013 (78 FR 64604), with an effective date 12-months after publication
of the final rule. These CoPs which are based on criteria prescribed in
law and are standards designed to ensure that each facility has
properly trained staff to provide the appropriate safe physical
environment for patients. These particular standards reflect comparable
standards developed by industry organizations such as the Joint
Commission. The primary users of this information will be State agency
surveyors, CMS and CMHCs for the purpose of ensuring compliance with
Medicare CoPs as well as ensuring the quality of care provided by CMHCs
to patients. Form Number: CMS-10506 (OMB Control number: 0938-1245);
Frequency: Occasionally; Affected Public: Private sector--Business or
other for-profits and Not-for-profit organizations; Number of
Respondents: 68; Total Annual Responses: 18,586; Total Annual Hours:
2,091. (For policy questions regarding this collection contact Mary
Rossi-Coajou at 410-786-6051.)
[[Page 22836]]
Dated: May 15, 2017.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2017-10085 Filed 5-17-17; 8:45 am]
BILLING CODE 4120-01-P