Agency Information Collection Activities; Proposals, Submissions, and Approvals:
Federal Register: November 29, 2010 (Volume 75, Number 228)
Notices
Page 73111-73112
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
DOCID:fr29no10-110
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
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
September 21, 2010, pages 57470-57472 and allowed 60 days for public comments. One comment regarding the use of government resources 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: Extension (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, NIH intramural collaborators, private physicians or organizations who refer patients to the Clinical Center, volunteers, vendors and collaborating commercial enterprises, small businesses, regulators, and other organizations. The annual reporting burden is as follows:
Number of
Frequency of
Average time
Annual hour
Customer
respondents
response
per response
burden
FY 2010
Clinical Center Patients........................
5000
1
.5
2500
Family Members of Patients......................
2000
1
.5
1000
Visitors to the Clinical Center.................
1000
1
.17
170
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.......................................
14,805 .............. ..............
5,824
Page 73112
FY 2011
Clinical Center Patients........................
5000
1
.5
2500
Family Members of Patients......................
3000
1
.5
1500
Visitors to the Clinical Center.................
1500
1
.17
255
NIH Intramural Collaborators....................
1500
1
.25
375
Vendors and Collaborating Commercial Enterprises
1000
1
.25
250
Professionals and Organizations Referring
3000
1
.33
1000
Patients.......................................
Regulators......................................
30
1
.33
10
Volunteers......................................
275
1
.33
92
Total.......................................
15,305 .............. ..............
5,982
FY 2012
Clinical Center Patients........................
5000
1
.5
2500
Family Members of Patients......................
2000
1
.5
1000
Visitors to the Clinical Center.................
1000
1
.17
170
NIH Intramural Collaborators....................
1000
1
.17
170
Vendors and Collaborating Commercial Enterprises
2500
1
.25
625
Professionals and Organizations Referring
3000
1
.33
1000
Patients.......................................
Regulators......................................
25
1
.25
6
Volunteers......................................
300
1
.25
75
Total.......................................
14,825 .............. ..............
5,546
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 each year for which the generic clearance is requested is $127,885 for 2010,
$126,895 for 2011, and $120,730 for 2012. Estimated Capital Costs are
$7,000. Estimated Operating and Maintenance costs are $75,000.
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, OIRA_submission@omb.eop.gov or by fax to 202-395-6974,
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: November 22, 2010.
David K. Henderson,
Deputy Director for Clinical Care, CC, National Institutes of Health.
FR Doc. 2010-29953 Filed 11-26-10; 8:45 am
BILLING CODE 4140-01-P
