Clinical Center; Submission for OMB Review; Comment Request Customer and Other Partners Satisfaction Surveys, 40886-40887 [E7-14364]
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40886
Federal Register / Vol. 72, No. 142 / Wednesday, July 25, 2007 / Notices
TABLE 1.—ESTIMATED ANNUAL RECORDKEEPING BURDEN1—Continued
21 CFR Sections
No. of
Recordkeepers
Annual Frequency
of Recordkeeping
Total Annual
Records
Hours per
Record
Total Hours
120.10(c) and 120.12(a)(4)(ii)
and (b)
1,840
12
22,080
0.1
2,208
120.11(a)(1)(iv) and (a)(2)
and 120.12(a)(5)
1,840
52
95,680
0.1
9,568
120.11(b) and 120.12(a)(5)
and (b)
1,840
1
1,840
4
7,360
120.11(c) and 120.12(a)(5)
and (b)
1,840
1
1,840
4
7,360
308
1
308
4
1,232
120.14(a)(2), (c), and (d)
Total
1There
358,466
are no capital costs or operating and maintenance costs associated with this collection of information.
rwilkins on PROD1PC63 with NOTICES
Table 1 of this document provides a
breakdown of the total estimated annual
recordkeeping burden. FDA bases this
hour burden estimate on its experience
with the application of HACCP
principles in food processing.
The burden estimates in table 1 of this
document are based on an estimate of
the total number of juice manufacturing
plants (i.e., 2,300) affected by the
regulations. Included in this total are
850 plants currently identified in FDA’s
official establishment inventory plus
1,220 very small apple juice
manufacturers and 230 very small
orange juice manufacturers. The total
burden hours are derived by estimating
the number of plants affected by each
portion of this final rule and
multiplying the corresponding number
by the number of records required
annually and the hours needed to
complete the record. These numbers
were obtained from the agency’s final
regulatory impact analysis prepared for
these regulations.
Moreover, these estimates assume that
every processor will prepare sanitary
standard operating procedures and a
HACCP plan and maintain the
associated monitoring records and that
every importer will require product
safety specifications. In fact, there are
likely to be some small number of juice
processors that, based upon their hazard
analysis, determine that they are not
required to have a HACCP plan under
these regulations.
Dated: July 19, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–14403 Filed 7–24–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Clinical Center; Submission for OMB
Review; Comment Request Customer
and Other Partners Satisfaction
Surveys
SUMMARY: In compliance with the
requirement of Section 3507(A)(1)(D) of
the Paperwork Reduction Act of 1995
for the opportunity for pubic comment
on the proposed data collection projects,
the Clinical Center (CC) of the National
Institutes of Health, (NIH) has submitted
to the Office of Management and Budget
(OMB) a request to review and approve
the information collection listed below.
This proposed information collection
was previously published in the Federal
Register on May 9, 2007 (Volume 72,
page 26400–26401) and allowed 60days for public comments. One
comment regarding resources required
to conduct surveys was received during
the 60-day comment period. The
purpose of this notice is to provide an
additional 30 days for public comment.
5 CFR 1320.5 Respondents to this
request for information collection
should not respond unless the request
displays a currently valid OMB control
number.
Proposed Collection: Title: Generic
Clearance for Satisfaction Surveys of
Customer and Other Partners. Type of
Information Collection Request:
Reinstatement (OMB Control Number:
0925–0458). Need and Use of
Information Collection: The information
collected in these surveys will be used
by Clinical Center personnel: (1) To
evaluate the satisfaction of various
Clinical Center customers and other
partners with Clinical Center services;
(2) to assist with the design of
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Fmt 4703
Sfmt 4703
modifications of these services, based
on customer input; (3) to develop new
services, based on customer need; and
4) to evaluate the satisfaction of various
Clinical Center customers and other
partners with implemented service
modifications. These surveys will
almost certainly lead to quality
improvement activities that will
enhance and/or streamline the Clinical
Center’s operations. The major
mechanisms by which the Clinical
Center will request customer input is
through surveys and focus groups. The
surveys will be tailored specifically to
each class of customer and to that class
of customer’s needs. Surveys will either
be collected as written documents, as
faxed documents, mailed electronically
or collected by telephone from
customers. Information gathered from
these surveys of Clinical Center
customers and other partners will be
presented to, and used directly by,
Clinical Center management to enhance
the services and operations of our
organization. Frequency of Response:
The participants will respond yearly.
Affected public: Individuals and
households, businesses and other for
profit, small businesses and
organizations. Types of respondents:
These surveys are designed to assess the
satisfaction of the Clinical Center’s
major internal and external customers
with the services provided. These
customers include, but are not limited
to, the following groups of individuals:
Clinical Center patients, family
members of Clinical Center patients,
visitors to the Clinical Center, National
Institutes of Health investigators, NIH
intramural collaborators, private
physicians or organizations who refer
patients to the Clinical Center,
volunteers, vendors and collaborating
commercial enterprises, small
E:\FR\FM\25JYN1.SGM
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40887
Federal Register / Vol. 72, No. 142 / Wednesday, July 25, 2007 / Notices
businesses, regulators, and other
organizations. The annual reporting
burden is as follows:
FY 2007
Number of respondents
Customer
Frequency of
response
Average time
per response
Annual hour
burden
5000
2000
1000
2500
2000
2000
2500
2000
30
275
1
1
1
1
1
1
1
1
1
1
.5
.5
.17
.25
.25
.17
.33
.33
.33
.5
2500
1000
170
625
625
340
833
833
10
138
Total ..........................................................................................................
rwilkins on PROD1PC63 with NOTICES
Clinical Center Patients ...................................................................................
Family Members of Patients ............................................................................
Visitors to the Clinical Center ..........................................................................
Clinical Center Employees ..............................................................................
NIH Investigators .............................................................................................
NIH Intramural Collaborators ...........................................................................
Vendors and Collaborating Commercial Enterprises ......................................
Professionals and Organizations Referring Patients .......................................
Regulators ........................................................................................................
Volunteers ........................................................................................................
19,305
........................
........................
7074
Estimated costs to the respondents
consists of their time; time is estimated
using a rate of $10.00 per hour for
patients and the public; $30.00 for
vendors, regulators, organizations and
$55.00 for health care professionals. The
estimated annual costs to respondents
for FY 2007 for which the generic
clearance is requested is $159,250.
Estimated Capital Costs are $7,000.
Estimated Operating and Maintenance
costs are $73,000.
Requests 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 functions of the
Clinical Center and the agency,
including whether the information shall
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 automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs, New Executive
Office Building, Room 10235,
Washington, DC 20503, Attention: Desk
Officer for NIH. To request more
information on the proposed project or
to obtain a copy of the data collection
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plans and instruments, contact: Dr.
David K. Henderson, Deputy Director
for Clinical Care, National Institutes of
Health Clinical Center, Building 10,
Room 6–1480, 10 Center Drive,
Bethesda, Maryland 20892, or call nontoll free: 301–496–3515, or e-mail your
request or comments, including your
address to: dkh@nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30 days of the date of
this publication.
Dated: July 18, 2007.
David K. Henderson,
Deputy Director for Clinical Care, CC,
National Institutes of Health.
[FR Doc. E7–14364 Filed 7–24–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; NICHD Research Partner
Satisfaction Surveys
SUMMARY: 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
National Institute of Child Health and
Human Development (NICHD), 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: NICHD
Research Partner Satisfaction Surveys.
Type of Information Collection Request:
RENEWAL of OMB Clearance 0925–
0532. Need and Use of Information
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Collection: Executive Order 12862
directs agencies that provide significant
services directly to the public to survey
customers to determine the kind and
quality of services they want and their
level of satisfaction with existing
services. With this submission, the
National Institute of Child Health and
Human Development (NICHD), Office of
Science Policy, Analysis and
Communication (OSPAC), seeks to
obtain OMB’s generic approval to
conduct customer satisfaction surveys
surrounding its research programs and
activities.
The NICHD was founded in 1963. Its
mission is to ensure, through research,
the birth of healthy infants and the
opportunity for each to reach full
potential in adulthood, unimpaired by
physical or mental disabilities. The
NICHD conducts and supports research
on the many factors that protect and
enhance the processes of human growth
and development. The developmental
focus of the NICHD means that its
research portfolio is unusually broad.
NICHD programs include research on
infant mortality, birth defects, learning
disorders, developmental disabilities,
vaccine development, and demographic
and behavioral sciences, among others.
In addition to supporting laboratory
research, clinical trials, and
epidemiological studies that explore
health processes, the NICHD
disseminates information that emanates
from its research programs to its
customers, or those who are partners
with the Institute. This includes
scientists, practitioners, other health
professionals, and the public.
Survey information will augment the
NICHD’s on-going efforts to assess their
research funding mechanisms,
activities, and programs, as well as the
information products that are used to
disseminate research findings. Primary
E:\FR\FM\25JYN1.SGM
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Agencies
[Federal Register Volume 72, Number 142 (Wednesday, July 25, 2007)]
[Notices]
[Pages 40886-40887]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-14364]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Clinical Center; Submission for OMB Review; Comment Request
Customer and Other Partners Satisfaction Surveys
SUMMARY: In compliance with the requirement of Section 3507(A)(1)(D) of
the Paperwork Reduction Act of 1995 for the opportunity for pubic
comment on the proposed data collection projects, the Clinical Center
(CC) of the National Institutes of Health, (NIH) has submitted to the
Office of Management and Budget (OMB) a request to review and approve
the information collection listed below. This proposed information
collection was previously published in the Federal Register on May 9,
2007 (Volume 72, page 26400-26401) and allowed 60- days for public
comments. One comment regarding resources required to conduct surveys
was received during the 60-day comment period. The purpose of this
notice is to provide an additional 30 days for public comment.
5 CFR 1320.5 Respondents to this request for information collection
should not respond unless the request displays a currently valid OMB
control number.
Proposed Collection: Title: Generic Clearance for Satisfaction
Surveys of Customer and Other Partners. Type of Information Collection
Request: Reinstatement (OMB Control Number: 0925-0458). Need and Use of
Information Collection: The information collected in these surveys will
be used by Clinical Center personnel: (1) To evaluate the satisfaction
of various Clinical Center customers and other partners with Clinical
Center services; (2) to assist with the design of modifications of
these services, based on customer input; (3) to develop new services,
based on customer need; and 4) to evaluate the satisfaction of various
Clinical Center customers and other partners with implemented service
modifications. These surveys will almost certainly lead to quality
improvement activities that will enhance and/or streamline the Clinical
Center's operations. The major mechanisms by which the Clinical Center
will request customer input is through surveys and focus groups. The
surveys will be tailored specifically to each class of customer and to
that class of customer's needs. Surveys will either be collected as
written documents, as faxed documents, mailed electronically or
collected by telephone from customers. Information gathered from these
surveys of Clinical Center customers and other partners will be
presented to, and used directly by, Clinical Center management to
enhance the services and operations of our organization. Frequency of
Response: The participants will respond yearly. Affected public:
Individuals and households, businesses and other for profit, small
businesses and organizations. Types of respondents: These surveys are
designed to assess the satisfaction of the Clinical Center's major
internal and external customers with the services provided. These
customers include, but are not limited to, the following groups of
individuals: Clinical Center patients, family members of Clinical
Center patients, visitors to the Clinical Center, National Institutes
of Health investigators, NIH intramural collaborators, private
physicians or organizations who refer patients to the Clinical Center,
volunteers, vendors and collaborating commercial enterprises, small
[[Page 40887]]
businesses, regulators, and other organizations. The annual reporting
burden is as follows:
FY 2007
----------------------------------------------------------------------------------------------------------------
Number of Frequency of Average time Annual hour
Customer respondents response per response burden
----------------------------------------------------------------------------------------------------------------
Clinical Center Patients........................ 5000 1 .5 2500
Family Members of Patients...................... 2000 1 .5 1000
Visitors to the Clinical Center................. 1000 1 .17 170
Clinical Center Employees....................... 2500 1 .25 625
NIH Investigators............................... 2000 1 .25 625
NIH Intramural Collaborators.................... 2000 1 .17 340
Vendors and Collaborating Commercial Enterprises 2500 1 .33 833
Professionals and Organizations Referring 2000 1 .33 833
Patients.......................................
Regulators...................................... 30 1 .33 10
Volunteers...................................... 275 1 .5 138
---------------------------------------------------------------
Total....................................... 19,305 .............. .............. 7074
----------------------------------------------------------------------------------------------------------------
Estimated costs to the respondents consists of their time; time is
estimated using a rate of $10.00 per hour for patients and the public;
$30.00 for vendors, regulators, organizations and $55.00 for health
care professionals. The estimated annual costs to respondents for FY
2007 for which the generic clearance is requested is $159,250.
Estimated Capital Costs are $7,000. Estimated Operating and Maintenance
costs are $73,000.
Requests 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 functions of the Clinical
Center and the agency, including whether the information shall 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 automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, New Executive Office Building, Room 10235, Washington, DC
20503, Attention: Desk Officer for NIH. To request more information on
the proposed project or to obtain a copy of the data collection plans
and instruments, contact: Dr. David K. Henderson, Deputy Director for
Clinical Care, National Institutes of Health Clinical Center, Building
10, Room 6-1480, 10 Center Drive, Bethesda, Maryland 20892, or call
non-toll free: 301-496-3515, or e-mail your request or comments,
including your address to: dkh@nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30 days
of the date of this publication.
Dated: July 18, 2007.
David K. Henderson,
Deputy Director for Clinical Care, CC, National Institutes of Health.
[FR Doc. E7-14364 Filed 7-24-07; 8:45 am]
BILLING CODE 4140-01-P