# Warren Grant Magnuson Clinical Center; Proposed Collection; Comment Request; Customer and Other Partners Satisfaction Surveys > Briefs, arguments, decisions, and more. URL: https://www.frixlaw.com/law-library/documents/fr%3A03-31322 ## Record - **Collection:** Federal Register - **Document type:** Notice - **Published:** December 19, 2003 - **Citation:** 68 FR 70821 ## Text DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Warren Grant Magnuson Clinical Center; Proposed Collection; Comment Request; Customer and Other Partners Satisfaction Surveys Summary: In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 for the opportunity for pubic comment on the proposed data collection projects, the Warren Grant Magnuson Clinical Center (CC), 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: Customer and Other Partners Satisfaction Surveys. Type of Information Collection Request: New request/waiver. 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 businesses, regulators, and other organizations. The annual reporting burden is as follows: Customer Type of survey Estimated number to be surveyed Expected response rate (percent) Time to complete survey (minutes) Estimated burden hours FY 2004 Clinical Center Patients Questionnaire 5000 50 30 1250 Family Members of Patients Questionnaire 3000 50 30 750 Visitors to the Clinical Center Questionnaire 1500 15 10 37.5 Clinical Center Employees Questionnaire/Electronic 2500 60 20 501 NIH Investigators Questionnaire/Electronic 2400 25 30 300 NIH Intramural Collaborators Questionnaire/Electronic 1500 30 15 112.5 Vendors and Collaborating Commercial Enterprises Questionnaire 2000 20 15 100 Professionals and Organizations Referring Patients Questionnaire/Electronic 1000 30 20 100.2 Regulators Questionnaire/Electronic 30 85 20 8.5 Volunteers Questionnaire 275 60 20 55.11 Total 19,205 3215.01 FY 2005 Clinical Center Patients Questionnaire/Electronic 5000 50 30 1250 Family Members of Patients Questionnaire/Electronic 2000 50 30 500 Visitors to the Clinical Center Questionnaire/Electronic 1000 15 10 25 Clinical Center Employees Questionnaire/Electronic 2500 60 20 501 NIH Investigators Questionnaire/Electronic 2500 25 20 208.75 NIH Intramural Collaborators Questionnaire/Electronic 1000 30 10 50.1 Vendors and Collaborating Commercial Enterprises Questionnaire/Electronic 2500 20 15 125 Professionals and Organizations Referring Patients Questionnaire/Electronic 3000 30 20 300.6 Regulators Questionnaire/Electronic 25 80 15 5 Volunteers Questionnaire/Electronic 300 50 15 37.5 Total 19,825 3002.95 FY 2006 Clinical Center Patients Questionnaire/Electronic 5000 60 30 1500 Family Members of Patients Questionnaire/Electronic 2000 40 30 400 Visitors to the Clinical Center Questionnaire/Electronic 1000 15 10 25.05 Clinical Center Employees Questionnaire/Electronic 2500 60 15 375 NIH Investigators Questionnaire/Electronic 2000 25 15 125 NIH Intramural Collaborators Questionnaire/Electronic 2000 30 10 100.2 Vendors and Collaborating Commercial Enterprises Questionnaire/Electronic 2500 15 20 125.25 Professionals and Organizations Referring Patients Questionnaire/Electronic 2000 30 20 200.4 Regulators Questionnaire/Electronic 30 85 205 8.5 Volunteers Questionnaire/Electronic 275 60 30 82.5 Total 19,305 2,941.9 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 $27,187.10 for 2004, $31,043 for 2005, and $24,693.70 for 2006. 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. FOR FURTHER INFORMATION CONTACT: 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, Warren G. Magnuson Clinical Center, National Institutes of Health, Building 10, Room 2C 146, 9000 Rockville Pike, 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 60 days of the date of this publication. Dated: December 11, 2003. David K. Henderson, Deputy Director for Clinical Care, CC, National Institutes of Health. [FR Doc. 03-31322 Filed 12-18-03; 8:45 am] BILLING CODE 4140-10-P --- Source: Frix Law Library, https://www.frixlaw.com/law-library/documents/fr%3A03-31322. Public record. Not legal advice.