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, 22836-22837 [2017-10040]
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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
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13:43 May 17, 2017
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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
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use of automated collection techniques
or other forms of information
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22837
Federal Register / Vol. 82, No. 95 / Thursday, May 18, 2017 / Notices
technology to minimize the information
collection burden.
Jason E. Bennett,
Director, Division of the Executive Secretariat.
[FR Doc. 2017–10040 Filed 5–17–17; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission to OMB for
Review and Approval; Public Comment
Request; Ryan White HIV/AIDS
Program Part F Dental Services
Report, OMB No. 0915-0151—
Extension
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995,
HRSA has submitted an Information
Collection Request (ICR) to the Office of
Management and Budget (OMB) for
review and approval. Comments
submitted during the first public review
of this ICR will be provided to OMB.
OMB will accept further comments from
the public during the review and
approval period.
DATES: Comments on this ICR should be
received no later than June 19, 2017.
ADDRESSES: Submit your comments,
including the ICR Title, to the desk
officer for HRSA, either by email to
OIRA_submission@omb.eop.gov or by
fax to 202–395–5806.
FOR FURTHER INFORMATION CONTACT: To
request a copy of the clearance requests
submitted to OMB for review, email the
HRSA Information Collection Clearance
Officer at paperwork@hrsa.gov or call
(301) 443–1984.
SUMMARY:
When
submitting comments or requesting
information, please include the
information request collection title for
reference, in compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995.
Information Collection Request Title:
Ryan White HIV/AIDS Program Part F
Dental Services Report, OMB No. 0915–
0151—Extension.
Abstract: The Dental Reimbursement
Program (DRP) and the CommunityBased Dental Partnership Program
(CBDPP) under Part F of the Ryan White
HIV/AIDS Program (RWHAP) offer
funding to accredited dental schools
and other accredited dental education
programs to support the provision of
oral health services for people living
with HIV as well as the education and
training of oral health providers in HIV
oral health care. Institutions eligible for
these RWHAP Part F funds are
accredited schools of dentistry and
other accredited dental education
programs, such as dental hygiene
programs or those sponsored by a school
of dentistry, a hospital, or a public or
private institution that offers
postdoctoral training in the specialties
of dentistry, advanced education in
general dentistry, or a dental general
practice residency. The Dental Services
Report (DSR) collects data on program
information, client demographics, oral
health services, funding, and training.
Awards are authorized under section
2692(b) of the Public Health Service Act
(42 U.S.C. 300ff–111(b)).
Need and Proposed Use of the
Information: The primary purpose of
collecting this information annually is
to verify applicant eligibility and
determine reimbursement amounts for
DRP applicants, as well as to document
the program accomplishments of CBDPP
grant recipients. This information also
allows HRSA to learn about (1) the
extent of the involvement of dental
schools and programs in treating
SUPPLEMENTARY INFORMATION:
patients with HIV, (2) the number and
characteristics of clients who receive
RWHAP-supported oral health services,
(3) the types and frequency of the
provision of these services, (4) the nonreimbursed costs of oral health care
provided to patients living with HIV,
and (5) the scope of grant recipients’
community-based collaborations and
training of providers. In addition to
meeting the goal of accountability to
Congress, clients, public and
community groups, and the general
public, information collected in the DSR
is critical for HRSA, state and local
grantees, and individual providers to
help assess the status of existing HIVrelated health service delivery systems.
Likely Respondents: Accredited
schools of dentistry and other
accredited dental education programs,
such as dental hygiene programs or
those sponsored by a school of
dentistry, a hospital, or a public or
private institution that offers
postdoctoral training in the specialties
of dentistry, advanced education in
general dentistry, or a dental general
practice residency.
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 review instructions; to
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; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. As this ICR is an extension,
the total burden hours are unchanged.
The total annual burden hours
estimated for this ICR are summarized
in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total
responses
Total burden
hours
Type of respondent
Dental Services Report .......
jstallworth on DSK7TPTVN1PROD with NOTICES
Form name
DRP ....................................
CBDPP ...............................
56
12
1
1
56
12
45
35
2,520
420
Total .............................
.............................................
68
........................
68
........................
2,940
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]]>Agencies
[Federal Register Volume 82, Number 95 (Thursday, May 18, 2017)]
[Notices]
[Pages 22836-22837]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-10040]
-----------------------------------------------------------------------
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
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: 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.
DATES: Comments on this ICR should be received no later than July 17,
2017.
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance Officer, Room 14N39, 5600 Fishers
Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: 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 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 long-term 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
----------------------------------------------------------------------------------------------------------------
Average number Average burden
Form name Number of of responses Total number per response Total burden
respondents per respondent of responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Potential Living Donor 14 55 770 1 770
Registration form..............
Potential Living Donor Follow-up 776 1 776 .50 388
form...........................
-------------------------------------------------------------------------------
Total....................... * 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 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 use of automated
collection techniques or other forms of information
[[Page 22837]]
technology to minimize the information collection burden.
Jason E. Bennett,
Director, Division of the Executive Secretariat.
[FR Doc. 2017-10040 Filed 5-17-17; 8:45 am]
BILLING CODE 4165-15-P
