Agency Information Collection Activities: Submission for OMB Review; Comment Request, 55584-55585 [2010-22665]
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55584
Federal Register / Vol. 75, No. 176 / Monday, September 13, 2010 / Notices
Number of
respondents
Application
Total ..........................................................................
E-mail comments to
paperwork@hrsa.gov or mail the HRSA
Reports Clearance Officer, Room 10–33,
Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments
should be received within 60 days of
this notice.
Dated: September 3, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–22662 Filed 9–10–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources
and Services Administration (HRSA)
publishes abstracts of information
collection requests under review by the
Office of Management and Budget
(OMB), in compliance with the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35). To request a copy of
the clearance requests submitted to
mstockstill on DSKB9S0YB1PROD with NOTICES
10
Number of
respondents
Jkt 220001
1
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Responses per
respondent
58
58
58
58
308
308
156
156
127
68
51
127
127
241
241
241
129
129
129
143
143
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143
44
44
44
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Fmt 4703
216
12
161
168
39
50
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196
35
42
2
36
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183
83
742
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58
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14
7
85
7
3
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7
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28
Sfmt 4703
Hours per
response
10
Proposed Project: Organ Procurement
and Transplantation Network and
Scientific Registry of Transplant
Recipients Data System (OMB No.
0915–0157)—Extension
Section 372 of the Public Health
Service (PHS) Act requires that the
Secretary, by contract, provide for the
establishment and operation of an Organ
Procurement and Transplantation
Network (OPTN). The OPTN, among
other responsibilities, operates and
maintains a national waiting list of
individuals requiring organ transplants,
maintains a computerized system for
matching donor organs with transplant
candidates on the waiting list, and
operates a 24-hour system to facilitate
matching organs with individuals
included in the list.
Data for the OPTN data system are
collected from transplant hospitals,
organ procurement organizations, and
tissue-typing laboratories. The
information is used to indicate the
Deceased Donor Registration ......................................
Death referral data .......................................................
Death Notification Referral—Eligible ...........................
Death Notification Referral—Imminent ........................
Living Donor Registration ............................................
Living Donor Follow-up ................................................
Donor Histocompatibility ..............................................
Recipient Histocompatibility .........................................
Heart Candidate Registration ......................................
Lung Candidate Registration .......................................
Heart/Lung Candidate Registration .............................
Thoracic Registration ...................................................
Thoracic Follow-up .......................................................
Kidney Candidate Registration ....................................
Kidney Registration ......................................................
Kidney Follow-up* ........................................................
Liver Candidate Registration .......................................
Liver Registration .........................................................
Liver Follow-up .............................................................
Kidney/Pancreas Candidate Registration ....................
Kidney/Pancreas Registration ......................................
Kidney/Pancreas Follow-up .........................................
Pancreas Candidate Registration ................................
Pancreas Registration ..................................................
Pancreas Follow-up .....................................................
Intestine Candidate Registration ..................................
Intestine Registration ...................................................
Intestine Follow-up .......................................................
17:21 Sep 10, 2010
Total
responses
OMB for review, e-mail
paperwork@hrsa.gov or call the HRSA
Reports Clearance Office on (301) 443–
1129.
The following request has been
submitted to the Office of Management
and Budget for review under the
Paperwork Reduction Act of 1995:
Form
VerDate Mar<15>2010
Responses per
respondent
6.5
Total burden
hours
60
disease severity of transplant
candidates, to monitor compliance of
member organizations with OPTN rules
and requirements, and to report
periodically on the clinical and
scientific status of organ donation and
transplantation in this country. Data are
used to develop transplant, donation
and allocation policies, to determine if
institutional members are complying
with policy, to determine memberspecific performance, to ensure patient
safety when no alternative sources of
data exist and to fulfill the requirements
of the OPTN Final Rule. 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 others for evaluation,
research, patient information, and other
important purposes.
No revisions of the 29 data collection
forms are proposed at this time;
however, the OPTN is currently
undergoing a review of the forms and
expects to submit proposed revisions
within the next year.
The annual estimate of burden is as
follows:
Total
responses
Hours per
response
12,528
696
9338
9744
12,012
15,400
20,436
30,576
4,445
2,856
102
4,572
40,640
44,103
20,003
178,822
14,061
7,482
66,951
2,002
1,001
12,155
1,001
429
2,860
308
220
1,232
E:\FR\FM\13SEN1.SGM
13SEN1
0.7500
10.0000
0.2000
0.5000
0.6500
0.5000
0.1000
0.2000
0.5000
0.5000
0.5000
0.7500
0.6500
0.5000
0.7500
0.5500
0.5000
0.6500
0.5000
0.5000
0.9000
0.8500
0.5000
0.7500
0.6500
0.5000
0.9000
0.8500
Total burden
hours
9,396.0000
6,960.0000
1,867.6000
4,872.0000
7,807.8000
7,700.0000
2,043.6000
6,115.2000
2,222.5000
1,428.0000
51.0000
3,429.0000
26,416.0000
22,051.5000
15,002.2500
98,352.1000
7,030.5000
4,863.3000
33,475.5000
1,001.0000
900.9000
10,331.7500
500.5000
321.7500
1,859.0000
154.0000
198.0000
1,047.2000
Federal Register / Vol. 75, No. 176 / Monday, September 13, 2010 / Notices
Number of
respondents
Form
Responses per
respondent
Total
responses
Hours per
response
55585
Total burden
hours
Post Transplant Malignancy ........................................
684
10
6,840
0.2000
1,368.0000
Total ......................................................................
463
............................
522,815
........................
278,765.9500
* Includes an estimated 2,500 kidney transplant patients transplanted prior to the initiation of the data system.
Written comments and
recommendations concerning the
proposed information collection should
be sent within 30 days of this notice to
the desk officer for HRSA, either by email to OIRA_submission@omb.eop.gov
or by fax to 202–395–6974. Please direct
all correspondence to the ‘‘attention of
the desk officer for HRSA.’’
Dated: September 3, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–22665 Filed 9–10–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; Generic Clearance for
Surveys of Customers and Partners of
the Office of Extramural Research of
the National Institutes of Health
In compliance with the
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
for opportunity for public comment on
proposed data collection projects, the
Office of Extramural Research (OER),
the National Institutes of Health (NIH)
will publish periodic summaries of
proposed projects to be submitted to the
Office of Management and Budget
(OMB) for review and approval.
Proposed Collection: Title: Generic
Clearance for Surveys of Customers and
Partners of the Office of Extramural
Research of the National Institutes of
Health. Type of Information Collection
Request: NEW. Need and Use of
Information Collection: OER develops,
coordinates the implementation of, and
evaluates NIH-wide policies and
procedures for the award of extramural
funds . To move forward with our
initiatives to ensure success in
accomplishing the NIH mission, input
from partners and customers is
essential. Quality management
principles have been integrated into
OER’s culture and these surveys will
provide customer satisfaction input on
various elements of OER’s business
processes. The approximately 14 (10
quantitative and 4 qualitative) customer
mstockstill on DSKB9S0YB1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
17:21 Sep 10, 2010
Jkt 220001
satisfaction surveys that will be
conducted under this generic clearance
will gather and measure customer and
partner satisfaction with OER processes
and operations. The data collected from
these surveys will provide the feedback
to track and gauge satisfaction with
NIH’s statutorily mandated operations
and processes. OER/OD/NIH will
present data and outcomes from these
surveys to inform the NIH staff, officers,
leadership, advisory committees, and
other decision-making bodies as
appropriate. Based on feedback from
these stakeholders, OER/OD/NIH will
formulate improvement plans and take
action when necessary. Frequency of
Response: 1 Response. Affected Public:
Individuals. Type of Respondents:
Science professionals (applicants,
reviewers, Institutional Officials), adult
science trainees, and the general public.
The annual reporting burden is as
follows:
Quantitative surveys:
Estimated Number of Respondents
per Survey: 9,820; Estimated Number of
Responses per Respondent: 1; Average
Burden Hours per Response: 0.25;
Estimated Total Annual Burden Hours
Requested per Quantitative Survey:
2,455; Estimated Total Annual Burden
Hours Requested for 10 Quantitative
Surveys: 24,550.
Qualitative surveys:
Estimated Number of Respondents
per Survey: 30; Estimated Number of
Responses per Respondent: 1; Average
Burden Hours per Response: 1.0;
Estimated Total Annual Burden Hours
Requested per Qualitative Survey: 30;
Estimated Total Annual Burden Hours
Requested for 4 Qualitative Surveys:
120.
Based on an estimated 10 quantitative
and 4 qualitative surveys per year:
Estimated Total Combined Annual
Hours of Burden Requested in Each of
3 years: 24,670.
Estimated Total Combined Cost to
Respondents: $728,326.
Based on an estimated 10 quantitative
and 4 qualitative surveys per year over
3 years:
Estimated Total Hours of Burden to
Respondents for 2011, 2012, and 2013
Combined: 74,010.
Estimated Total Cost to Respondents
for 2011, 2012, and 2013 Combined:
$2,184,978.
PO 00000
Frm 00047
Fmt 4703
Sfmt 9990
There are no Capital Costs to report.
There are no Operating or Maintenance
Costs to report.
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Whether the proposed collection of
information is necessary for the proper
performance of the function of the
agency, including whether the
information will have practical utility;
(2) The accuracy of the agency’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
Ways to minimize the burden of the
collection of information on those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
To
request more information on the
proposed generic clearance or to obtain
a copy of example data collection
instruments, contact Dr. Gwynne
Jenkins, Special Assistant to the
Director, Office of Extramural Programs,
OER, NIH, 6705 Rockledge Drive, Suite
350, Bethesda, MD 20892, or call nontoll-free number (301) 496–9232 or
E-mail your request, including your
address to: OEPMailbox@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60-days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT:
Dated: August 30, 2010.
Sherry Mills,
Director, Office of Extramural Programs.
[FR Doc. 2010–22712 Filed 9–10–10; 8:45 am]
BILLING CODE 4140–01–P
E:\FR\FM\13SEN1.SGM
13SEN1
Agencies
[Federal Register Volume 75, Number 176 (Monday, September 13, 2010)]
[Notices]
[Pages 55584-55585]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-22665]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources and Services Administration
(HRSA) publishes abstracts of information collection requests under
review by the Office of Management and Budget (OMB), in compliance with
the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request
a copy of the clearance requests submitted to OMB for review, e-mail
paperwork@hrsa.gov or call the HRSA Reports Clearance Office on (301)
443-1129.
The following request has been submitted to the Office of
Management and Budget for review under the Paperwork Reduction Act of
1995:
Proposed Project: Organ Procurement and Transplantation Network and
Scientific Registry of Transplant Recipients Data System (OMB No. 0915-
0157)--Extension
Section 372 of the Public Health Service (PHS) Act requires that
the Secretary, by contract, provide for the establishment and operation
of an Organ Procurement and Transplantation Network (OPTN). The OPTN,
among other responsibilities, operates and maintains a national waiting
list of individuals requiring organ transplants, maintains a
computerized system for matching donor organs with transplant
candidates on the waiting list, and operates a 24-hour system to
facilitate matching organs with individuals included in the list.
Data for the OPTN data system are collected from transplant
hospitals, organ procurement organizations, and tissue-typing
laboratories. The information is used to indicate the disease severity
of transplant candidates, to monitor compliance of member organizations
with OPTN rules and requirements, and to report periodically on the
clinical and scientific status of organ donation and transplantation in
this country. Data are used to develop transplant, donation and
allocation policies, to determine if institutional members are
complying with policy, to determine member-specific performance, to
ensure patient safety when no alternative sources of data exist and to
fulfill the requirements of the OPTN Final Rule. 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 others for evaluation,
research, patient information, and other important purposes.
No revisions of the 29 data collection forms are proposed at this
time; however, the OPTN is currently undergoing a review of the forms
and expects to submit proposed revisions within the next year.
The annual estimate of burden is as follows:
----------------------------------------------------------------------------------------------------------------
Number of Responses per Total Hours per Total burden
Form respondents respondent responses response hours
----------------------------------------------------------------------------------------------------------------
Deceased Donor Registration. 58 216 12,528 0.7500 9,396.0000
Death referral data......... 58 12 696 10.0000 6,960.0000
Death Notification Referral-- 58 161 9338 0.2000 1,867.6000
Eligible...................
Death Notification Referral-- 58 168 9744 0.5000 4,872.0000
Imminent...................
Living Donor Registration... 308 39 12,012 0.6500 7,807.8000
Living Donor Follow-up...... 308 50 15,400 0.5000 7,700.0000
Donor Histocompatibility.... 156 131 20,436 0.1000 2,043.6000
Recipient Histocompatibility 156 196 30,576 0.2000 6,115.2000
Heart Candidate Registration 127 35 4,445 0.5000 2,222.5000
Lung Candidate Registration. 68 42 2,856 0.5000 1,428.0000
Heart/Lung Candidate 51 2 102 0.5000 51.0000
Registration...............
Thoracic Registration....... 127 36 4,572 0.7500 3,429.0000
Thoracic Follow-up.......... 127 320 40,640 0.6500 26,416.0000
Kidney Candidate 241 183 44,103 0.5000 22,051.5000
Registration...............
Kidney Registration......... 241 83 20,003 0.7500 15,002.2500
Kidney Follow-up*........... 241 742 178,822 0.5500 98,352.1000
Liver Candidate Registration 129 109 14,061 0.5000 7,030.5000
Liver Registration.......... 129 58 7,482 0.6500 4,863.3000
Liver Follow-up............. 129 519 66,951 0.5000 33,475.5000
Kidney/Pancreas Candidate 143 14 2,002 0.5000 1,001.0000
Registration...............
Kidney/Pancreas Registration 143 7 1,001 0.9000 900.9000
Kidney/Pancreas Follow-up... 143 85 12,155 0.8500 10,331.7500
Pancreas Candidate 143 7 1,001 0.5000 500.5000
Registration...............
Pancreas Registration....... 143 3 429 0.7500 321.7500
Pancreas Follow-up.......... 143 20 2,860 0.6500 1,859.0000
Intestine Candidate 44 7 308 0.5000 154.0000
Registration...............
Intestine Registration...... 44 5 220 0.9000 198.0000
Intestine Follow-up......... 44 28 1,232 0.8500 1,047.2000
[[Page 55585]]
Post Transplant Malignancy.. 684 10 6,840 0.2000 1,368.0000
-----------------------------------------------------------------------------------
Total................... 463 ................ 522,815 .............. 278,765.9500
----------------------------------------------------------------------------------------------------------------
* Includes an estimated 2,500 kidney transplant patients transplanted prior to the initiation of the data
system.
Written comments and recommendations concerning the proposed
information collection should be sent within 30 days of this notice to
the desk officer for HRSA, either by e-mail to OIRA_submission@omb.eop.gov or by fax to 202-395-6974. Please direct all
correspondence to the ``attention of the desk officer for HRSA.''
Dated: September 3, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-22665 Filed 9-10-10; 8:45 am]
BILLING CODE 4165-15-P