Agency Information Collection Activities: Proposed Collection: Public Comment Request, 13378-13380 [2016-05684]
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Federal Register / Vol. 81, No. 49 / Monday, March 14, 2016 / Notices
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. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Form name
Number of
responses
per
respondent
Average
burden per
response
(in hours)
Total
responses
Total burden
hours
Direct Financial Support Program .......................................
Infrastructure Program .........................................................
Multipurpose or Hybrid Program ..........................................
618
149
790
1
1
1
618
149
790
3.117
4.57
4.285
1,926
681
3,385
Total ..............................................................................
1,557
........................
1,557
........................
5,992
Jackie Painter,
Director, Division of the Executive Secretariat.
[FR Doc. 2016–05602 Filed 3–11–16; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request
Health Resources and Services
Administration, HHS.
AGENCY:
ACTION:
Notice.
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects (Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995), the
Health Resources and Services
Administration (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 Information
Collection Request must be received
within 60 days of this notice.
DATES:
Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N39, Parklawn
Building, 5600 Fishers Lane, Rockville,
MD 20857.
jstallworth on DSK7TPTVN1PROD with NOTICES
ADDRESSES:
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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.
Information Collection Request Title:
Organ Procurement and Transplantation
Network and Scientific Registry of
Transplant Recipients Data System
OMB No. 0915–0157—Revision.
Abstract: Section 372 of the Public
Health Service (PHS) Act, as amended,
requires that the Secretary, by contract,
provide for the establishment and
operation of an Organ Procurement and
Transplantation Network (OPTN). This
is a request for revisions to current
OPTN data collection forms associated
with an individual’s clinical
characteristics at the time of
registration, transplant, and follow-up
after the transplant. These specific data
elements of the OPTN data system are
collected from transplant hospitals. The
information is used to indicate the
disease severity of transplant
candidates, to monitor compliance of
member organizations with OPTN rules
and requirements, to report periodically
on the clinical and scientific status of
organ donation and transplantation and
other purposes consistent with the law.
Data are used to: (1) Facilitate organ
placement and match donor organs with
recipients; (2) monitor compliance of
member organizations with federal laws
and regulations and with OPTN
requirements; (3) review and report
FOR FURTHER INFORMATION CONTACT:
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periodically to the public on the status
of organ donation and transplantation in
the United States; (4) provide data to
researchers and government agencies to
study the scientific and clinical status of
organ transplantation; and (5) perform
transplantation-related public health
surveillance including possible
transmission of donor disease. The
practical utility of the data collection is
further enhanced by requirements that
the OPTN data must be made available,
consistent with applicable laws, for use
by OPTN members, the Scientific
Registry of Transplant Recipients, the
Department of Health and Human
Services, and members of the public for
evaluation, research, patient
information, and other important
purposes.
Likely Respondents: 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.
E:\FR\FM\14MRN1.SGM
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Federal Register / Vol. 81, No. 49 / Monday, March 14, 2016 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Section/activity
Average
number of
responses per
respondent
Average
burden per
response
(in hours)
Total number
of responses
Total burden
hours
Deceased Donor Registration ..............................................
Living Donor Registration ....................................................
Living Donor Follow-up ........................................................
Donor Histocompatibility ......................................................
Recipient Histocompatibility .................................................
Heart Candidate Registration ..............................................
Heart Recipient Registration ............................................
Heart Follow Up (6 Month) ..................................................
Heart Follow Up (1–5 Year) .................................................
Heart Follow Up (Post 5 Year) ............................................
Heart Post-Transplant Malignancy Form .............................
Lung Candidate Registration ...............................................
Lung Recipient Registration .............................................
Lung Follow Up (6 Month) ................................................
Lung Follow Up (1–5 Year) ...............................................
Lung Follow Up (Post 5 Year) .............................................
Lung Post-Transplant Malignancy Form ..............................
Heart/Lung Candidate Registration .....................................
Heart/Lung Recipient Registration ...................................
Heart/Lung Follow Up (6 Month) ......................................
Heart/Lung Follow Up (1–5 Year) .....................................
Heart/Lung Follow Up (Post 5 Year) ...................................
Heart/Lung Post-Transplant Malignancy Form ....................
Liver Candidate Registration ...............................................
Liver Recipient Registration .............................................
Liver Follow-up (6 Month—5 Year) .....................................
Liver Follow-up (Post 5 Year) ..............................................
Liver Recipient Explant Pathology Form .............................
Liver Post-Transplant Malignancy .......................................
Intestine Candidate Registration ..........................................
Intestine Recipient Registration .......................................
Intestine Follow Up (6 Month—5 Year) ...............................
Intestine Follow Up (Post 5 Year) .......................................
Intestine Post-Transplant Malignancy Form ........................
Kidney Candidate Registration ............................................
Kidney Recipient Registration ..........................................
Kidney Follow-Up (6 Month—5 Year) ..................................
Kidney Follow-up (Post 5 Year) ...........................................
Kidney Post-Transplant Malignancy Form ...........................
Pancreas Candidate Registration ....................................
Pancreas Recipient Registration ......................................
Pancreas Follow-up (6 Month—5 Year) ...........................
Pancreas Follow-up (Post 5 Year) ......................................
Pancreas Post-Transplant Malignancy Form ......................
Kidney/Pancreas Candidate Registration .......................
Kidney/Pancreas Recipient Registration .........................
Kidney/Pancreas Follow-up (6 Month—5 Year) ..............
Kidney/Pancreas Follow-up (Post 5 Year) ..........................
Kidney/Pancreas Post-Transplant Malignancy Form ..........
VCA Candidate Registration ................................................
VCA Recipient Registration .................................................
VCA Recipient Follow Up ....................................................
58
307
307
154
154
132
132
132
132
132
132
70
70
70
70
70
70
69
69
69
69
69
69
141
141
141
141
141
141
40
40
40
40
40
238
238
238
238
238
141
141
141
141
141
141
141
141
141
141
23
23
23
158.2
20.6
60.7
96.7
173.5
30.5
19.9
17
73.9
115.2
11
39.6
28.3
26.2
99.4
65.6
1.5
0.7
0.4
0.3
1.5
3.1
0.2
89.2
48.8
231.1
256.5
12.3
13.2
4.4
3.4
13.3
13.5
0.6
162.6
71.8
379.5
346.7
18.1
3.4
1.8
8.2
13.5
0.8
9.6
5.2
26.9
48.2
1.6
1.7
1.7
1.7
9175.6
6324.2
18634.9
14891.8
26719
4026
2626.8
2244
9754.8
15206.4
1452
2772
1981
1834
6958
4592
105
48.3
27.6
20.7
103.5
213.9
13.8
12577.2
6880.8
32585.1
36166.5
1734.3
1861.2
176
136
532
540
24
38698.8
17088.4
90321
82514.6
4307.8
479.4
253.8
1156.2
1903.5
112.8
1353.6
733.2
3792.9
6796.2
225.6
39.1
39.1
39.1
1.1
1.8
1.3
0.2
0.4
0.9
1.2
0.4
0.9
0.5
0.9
0.9
1.2
0.5
1.1
0.6
0.4
1.1
1.3
0.8
1.1
0.6
0.4
0.8
1.2
1
0.5
0.6
0.8
1.3
1.8
1.5
0.4
1
0.8
1.2
0.9
0.5
0.8
0.6
1.2
0.5
0.5
0.6
0.6
1.2
0.5
0.6
0.4
0.4
1.3
1
10093.2
11383.6
24225.4
2978.4
10687.6
3623.4
3152.2
897.6
8779.3
7603.2
1306.8
2494.8
2377.2
917.0
7653.8
2755.2
42.0
53.1
35.9
16.6
113.9
128.3
5.5
10061.8
8257.0
32585.1
18083.3
1040.6
1489.0
228.8
244.8
798.0
216.0
24.0
30959.0
20506.1
81288.9
41257.3
3446.2
287.6
304.6
578.1
951.8
67.7
812.2
879.8
1896.5
4077.7
90.2
15.6
50.8
39.1
Total .............................................................................
* 457
........................
471411.4
........................
359889.5
jstallworth on DSK7TPTVN1PROD with NOTICES
* Total number of OPTN transplant hospitals as of October 23, 2015. Number of respondents for transplant candidate or recipient forms is
based on number of organ specific programs associated with each form.
** Bold entries represent those forms being modified during this submission.
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E:\FR\FM\14MRN1.SGM
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13380
Federal Register / Vol. 81, No. 49 / Monday, March 14, 2016 / Notices
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
technology to minimize the information
collection burden.
Jackie Painter,
Director, Division of the Executive Secretariat.
[FR Doc. 2016–05684 Filed 3–11–16; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS–OS–0990–new–
60D]
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, announces plans
to submit a new Information Collection
SUMMARY:
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting the ICR to
OMB, OS seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on the ICR must be
received on or before May 13, 2016.
ADDRESSES: Submit your comments to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–6162.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 690–6162.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
document identifier HHS–OS–0990–
new–60D for reference.
Information Collection Request Title:
Sustainability study of federally-funded
programs designed to prevent or delay
teen pregnancy (TPP Sustainability
Study).
Abstract: The Office of Adolescent
Health (OAH), U.S. Department of
Health and Human Services (HHS) is
requesting approval by OMB on a new
collection. The TPP Sustainability
Study is a key piece of OAH’s broad and
ongoing effort to comprehensively
evaluate all of its teen pregnancy
prevention funding efforts which
consist of: (1) The Teen Pregnancy
Prevention Program (TPP); the (2)
Pregnancy Assistance Fund (PAF); and
the Communitywide program funded
through OAH and the Centers for
Disease Control (CDC).
The proposed information request
includes instruments that will collect
data on: (1) Whether and how federallyfunded programs have been sustained;
(2) factors affecting program
sustainability; (3) methods and
strategies employed by grantees to
sustain programs; (4) support and
technical assistance that grantees
received related to sustaining the
programs; and (5) key lessons learned
based on the outcomes of these efforts.
The data will be analyzed and
incorporated into study deliverables
that clearly describe grantees’
sustainability efforts for all audiences
and highlight key challenges, successes,
and lessons learned for future funding
and program implementation.
The data will be used for the study
team to identify key factors in program
sustainability, the strategies that either
worked or did not work in sustaining
programs over time, and the types of
support and assistance grantees required
in order to sustain programs. Collecting
this data is crucial to closing an existing
gap in OAH knowledge about how to
support the sustainability efforts of
current and future grantees, including
the 2015–2020 TPP grantee cohort and
the 2013–2016 PAF cohort.
Likely Respondents: Program
administrators at 117 grantee
organizations.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Form name
Average
burden per
response
(in hours)
Number of
responses per
respondent
Total burden
hours
39
17
1
2
0.41
1.5
16.0
51.0
Total ........................................................................................................
jstallworth on DSK7TPTVN1PROD with NOTICES
Grantee Survey ..............................................................................................
In-Depth Interview Master Topic Guide .........................................................
56
........................
..........................
66.0
OS 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
technology to minimize the information
collection burden.
Terry S. Clark,
Asst Collection Clearance Officer.
[FR Doc. 2016–05603 Filed 3–11–16; 8:45 am]
BILLING CODE 4168–11–P
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Earliest Anticipated Start Date: June
1, 2016.
Indian Health Service
I. Funding Opportunity Description
Office of Urban Indian Health
Programs; 4-in-1 Grant Programs;
Announcement Type: New and
Competing Continuation Funding
Announcement Number: HHS–2016–
IHS–UIHP2–0001; Catalogue of Federal
Domestic Assistance Number: 93.193
Key Dates
Application Deadline Date: May 15,
2016.
Review Period: May 23, 2016–May 27,
2016.
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Statutory Authority
The Indian Health Service (IHS) is
accepting competitive grant applications
for the FY 2016 4-in-1 Title V Programs.
This program is authorized under the
Snyder Act, 25 U.S.C. 13, Public Law
67–85, and Title V of the Indian Health
Care Improvement Act (IHCIA), Public
Law 94–437, as amended, specifically
the provisions codified at 25 U.S.C.
1652, 1653, and 1660a. This program is
described in the Catalog of Federal
E:\FR\FM\14MRN1.SGM
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]]>Agencies
[Federal Register Volume 81, Number 49 (Monday, March 14, 2016)]
[Notices]
[Pages 13378-13380]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-05684]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request
AGENCY: Health Resources and Services Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects (Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995), the Health Resources and Services
Administration (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 Information Collection Request must be received
within 60 days of this notice.
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance Officer, Room 14N39, Parklawn
Building, 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.
Information Collection Request Title: Organ Procurement and
Transplantation Network and Scientific Registry of Transplant
Recipients Data System OMB No. 0915-0157--Revision.
Abstract: Section 372 of the Public Health Service (PHS) Act, as
amended, requires that the Secretary, by contract, provide for the
establishment and operation of an Organ Procurement and Transplantation
Network (OPTN). This is a request for revisions to current OPTN data
collection forms associated with an individual's clinical
characteristics at the time of registration, transplant, and follow-up
after the transplant. These specific data elements of the OPTN data
system are collected from transplant hospitals. The information is used
to indicate the disease severity of transplant candidates, to monitor
compliance of member organizations with OPTN rules and requirements, to
report periodically on the clinical and scientific status of organ
donation and transplantation and other purposes consistent with the
law. Data are used to: (1) Facilitate organ placement and match donor
organs with recipients; (2) monitor compliance of member organizations
with federal laws and regulations and with OPTN requirements; (3)
review and report periodically to the public on the status of organ
donation and transplantation in the United States; (4) provide data to
researchers and government agencies to study the scientific and
clinical status of organ transplantation; and (5) perform
transplantation-related public health surveillance including possible
transmission of donor disease. The practical utility of the data
collection is further enhanced by requirements that the OPTN data must
be made available, consistent with applicable laws, for use by OPTN
members, the Scientific Registry of Transplant Recipients, the
Department of Health and Human Services, and members of the public for
evaluation, research, patient information, and other important
purposes.
Likely Respondents: 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.
[[Page 13379]]
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average Average
Number of number of Total number burden per Total burden
Section/activity respondents responses per of responses response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Deceased Donor Registration..... 58 158.2 9175.6 1.1 10093.2
Living Donor Registration....... 307 20.6 6324.2 1.8 11383.6
Living Donor Follow-up.......... 307 60.7 18634.9 1.3 24225.4
Donor Histocompatibility........ 154 96.7 14891.8 0.2 2978.4
Recipient Histocompatibility.... 154 173.5 26719 0.4 10687.6
Heart Candidate Registration.... 132 30.5 4026 0.9 3623.4
Heart Recipient Registration.... 132 19.9 2626.8 1.2 3152.2
Heart Follow Up (6 Month)....... 132 17 2244 0.4 897.6
Heart Follow Up (1-5 Year)...... 132 73.9 9754.8 0.9 8779.3
Heart Follow Up (Post 5 Year)... 132 115.2 15206.4 0.5 7603.2
Heart Post-Transplant Malignancy 132 11 1452 0.9 1306.8
Form...........................
Lung Candidate Registration..... 70 39.6 2772 0.9 2494.8
Lung Recipient Registration..... 70 28.3 1981 1.2 2377.2
Lung Follow Up (6 Month)........ 70 26.2 1834 0.5 917.0
Lung Follow Up (1-5 Year)....... 70 99.4 6958 1.1 7653.8
Lung Follow Up (Post 5 Year).... 70 65.6 4592 0.6 2755.2
Lung Post-Transplant Malignancy 70 1.5 105 0.4 42.0
Form...........................
Heart/Lung Candidate 69 0.7 48.3 1.1 53.1
Registration...................
Heart/Lung Recipient 69 0.4 27.6 1.3 35.9
Registration...................
Heart/Lung Follow Up (6 Month).. 69 0.3 20.7 0.8 16.6
Heart/Lung Follow Up (1-5 Year). 69 1.5 103.5 1.1 113.9
Heart/Lung Follow Up (Post 5 69 3.1 213.9 0.6 128.3
Year)..........................
Heart/Lung Post-Transplant 69 0.2 13.8 0.4 5.5
Malignancy Form................
Liver Candidate Registration.... 141 89.2 12577.2 0.8 10061.8
Liver Recipient Registration.... 141 48.8 6880.8 1.2 8257.0
Liver Follow-up (6 Month--5 141 231.1 32585.1 1 32585.1
Year)..........................
Liver Follow-up (Post 5 Year)... 141 256.5 36166.5 0.5 18083.3
Liver Recipient Explant 141 12.3 1734.3 0.6 1040.6
Pathology Form.................
Liver Post-Transplant Malignancy 141 13.2 1861.2 0.8 1489.0
Intestine Candidate Registration 40 4.4 176 1.3 228.8
Intestine Recipient Registration 40 3.4 136 1.8 244.8
Intestine Follow Up (6 Month--5 40 13.3 532 1.5 798.0
Year)..........................
Intestine Follow Up (Post 5 40 13.5 540 0.4 216.0
Year)..........................
Intestine Post-Transplant 40 0.6 24 1 24.0
Malignancy Form................
Kidney Candidate Registration... 238 162.6 38698.8 0.8 30959.0
Kidney Recipient Registration... 238 71.8 17088.4 1.2 20506.1
Kidney Follow-Up (6 Month--5 238 379.5 90321 0.9 81288.9
Year)..........................
Kidney Follow-up (Post 5 Year).. 238 346.7 82514.6 0.5 41257.3
Kidney Post-Transplant 238 18.1 4307.8 0.8 3446.2
Malignancy Form................
Pancreas Candidate Registration. 141 3.4 479.4 0.6 287.6
Pancreas Recipient Registration. 141 1.8 253.8 1.2 304.6
Pancreas Follow-up (6 Month--5 141 8.2 1156.2 0.5 578.1
Year)..........................
Pancreas Follow-up (Post 5 Year) 141 13.5 1903.5 0.5 951.8
Pancreas Post-Transplant 141 0.8 112.8 0.6 67.7
Malignancy Form................
Kidney/Pancreas Candidate 141 9.6 1353.6 0.6 812.2
Registration...................
Kidney/Pancreas Recipient 141 5.2 733.2 1.2 879.8
Registration...................
Kidney/Pancreas Follow-up (6 141 26.9 3792.9 0.5 1896.5
Month--5 Year).................
Kidney/Pancreas Follow-up (Post 141 48.2 6796.2 0.6 4077.7
5 Year)........................
Kidney/Pancreas Post-Transplant 141 1.6 225.6 0.4 90.2
Malignancy Form................
VCA Candidate Registration...... 23 1.7 39.1 0.4 15.6
VCA Recipient Registration...... 23 1.7 39.1 1.3 50.8
VCA Recipient Follow Up......... 23 1.7 39.1 1 39.1
-------------------------------------------------------------------------------
Total....................... * 457 .............. 471411.4 .............. 359889.5
----------------------------------------------------------------------------------------------------------------
* Total number of OPTN transplant hospitals as of October 23, 2015. Number of respondents for transplant
candidate or recipient forms is based on number of organ specific programs associated with each form.
** Bold entries represent those forms being modified during this submission.
[[Page 13380]]
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 technology to
minimize the information collection burden.
Jackie Painter,
Director, Division of the Executive Secretariat.
[FR Doc. 2016-05684 Filed 3-11-16; 8:45 am]
BILLING CODE 4165-15-P
