Agency Information Collection Activities: Submission for OMB Review; Comment Request, 46944-46945 [2010-19121]

Download as PDF 46944 Federal Register / Vol. 75, No. 149 / Wednesday, August 4, 2010 / Notices demographic information and state of residency when customers subscribe to its email update service, for the purpose of assessing information needs and better targeting email messages to appropriate audiences. SAMHSA is employing a Web-based form for information collection to avoid duplication and unnecessary burden on customers who register both for an account on the product Web site and for e-mail updates. The Web technology allows SAMHSA to integrate the email update subscription process into the Web site account registration process. Customers who register for an account on the new product Web site will be given the option of being enrolled automatically to receive SAMHSA email updates. Any optional questions answered by the customer during the Web site registration process will automatically be mapped to the profile generated for the e-mail update system, thereby reducing the collection of duplicate information. SAMHSA will collect all customer information submitted for Web site registration and email update subscriptions electronically via a series of Web forms on the samhsa.gov domain. Customers can submit the Web forms at their leisure, or call SAMHSA’s toll-free Call Center and an information specialist will submit the forms on their behalf. The electronic collection of information will reduce the burden on the respondent and streamline the datacapturing process. SAMHSA will place Web site registration information into a Knowledge Management database and will place email subscription information into a database maintained by a third-party vendor that serves multiple Federal agencies and the White House. Customers can change, add, or delete their information from either system at any time. The respondents will be behavioral health professionals, researchers, parents, caregivers, and the general public. SAMHSA estimates the burden of this information collection as follows: TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN Annual frequency per response Number of respondents Total annual responses Hours per response Total hours Web Site Registration ....................................................... Email Update Subscription ............................................... 41,200 24,000 1 1 41,200 24,000 .033 (2 min.) ..... .017 (1 min.) ..... 1,360 480 Total ........................................................................... 65,200 ........................ 65,200 ........................... 1,840 Written comments and recommendations concerning the proposed information collection should be sent by September 3, 2010 to: SAMHSA Desk Officer, Human Resources and Housing Branch, Office of Management and Budget, New Executive Office Building, Room 10235, Washington, DC 20503; due to potential delays in OMB’s receipt and processing of mail sent through the U.S. Postal Service, respondents are encouraged to submit comments by fax to: 202–395– 5806. Dated: July 27, 2010. Elaine Parry, Director, Office of Program Services. [FR Doc. 2010–19118 Filed 8–3–10; 8:45 am] mstockstill on DSKH9S0YB1PROD with NOTICES BILLING CODE 4162–20–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 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: Scholarships for Disadvantaged Students (SDS) Program (OMB No. 0915–0149)—Extension The Scholarships for Disadvantaged Students (SDS) Program has as its Number of respondents Instrument Application ............................................................................ VerDate Mar<15>2010 16:26 Aug 03, 2010 Jkt 220001 PO 00000 Frm 00046 Responses per respondent 600 Fmt 4703 Sfmt 4703 purpose, the provision of funds to eligible schools to provide scholarships to full-time, financially needy students from disadvantaged backgrounds enrolled in health professions and nursing programs. To qualify for participation in the SDS program, a school must be carrying out a program for recruiting and retaining students from disadvantaged backgrounds, including students who are members of racial and ethnic minority groups (Section 737(d)(1)(B) of the Public Health Service (PHS) Act). A school must meet the eligibility criteria to demonstrate that the program has achieved success based on the number and/or percentage of disadvantaged students who graduate from the school. In awarding SDS funds to eligible schools, funding priorities must be given to schools based on the proportion of graduating students going into primary care, the proportion of underrepresented minority students, and the proportion of graduates working in medically underserved communities (Section 737(c) of the PHS Act). The annual estimate of burden is as follows: Total responses 1 E:\FR\FM\04AUN1.SGM 600 04AUN1 Hours per response Total burden hours 13 7,800 46945 Federal Register / Vol. 75, No. 149 / Wednesday, August 4, 2010 / Notices Number of respondents Instrument Responses per respondent Total responses Hours per response Total burden hours Report .................................................................................. 600 1 600 1 600 Total .............................................................................. 600 1 600 14 8,400 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: July 28, 2010. Sahira Rafiullah, Director, Division of Policy and Information Coordination. [FR Doc. 2010–19121 Filed 8–3–10; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; Comment Request; the Drug Accountability Record (Form NIH 2564) (NCI) In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, SUMMARY: for opportunity for public comment on proposed data collection projects, the National Cancer Institute (NCI), 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: The Drug Accountability Record (Form NIH 2564) (OMB No. 0925–0240). Type of Information Collection Request: Extension with changes. Need and Use of Information Collection: The Food and Drug Administration (FDA) regulations require investigators to establish a record of receipt, use and disposition of all investigational agents. The National Cancer Institute (NCI), as a sponsor of investigational agent trials, has the responsibility to assure the FDA that investigators in its clinical trials program are maintaining systems for agent accountability. In order to fulfill these requirements, a standard Investigational Drug Accountability Report Form (DARF) NIH–2564, was designed to account for agent inventories and usage by protocols. The data obtained from the agent accountability record will be used to keep track of the dispensing of investigational agent anticancer agents to patients. It is used by the NCI management to ensure that investigational agent supplies are not diverted for inappropriate protocol or patient use. The information is also compared to patient flow sheets (protocol reporting forms) during site visits conducted for each investigator every three years. All comparisons are done with the intention of ensuring protocol, patient and agent compliance for patient safety and protection. Frequency of Response: Approximately 16 times per year. Affected Public: Private sector including businesses, other for-profit organizations, and nonprofit institutions. Type of Respondents: Investigators, pharmacists, nurses, pharmacy technicians, and data managers. The annualized respondents’ burden for record keeping is estimated to require 6,714 hours (Table 1). There are no capital costs, operating costs, or maintenance costs to report. TABLE 1—ESTIMATES OF ANNUAL BURDEN HOURS Number of respondents Type of respondents Investigators, or Designees ............................................................................. mstockstill on DSKH9S0YB1PROD with NOTICES 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 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 VerDate Mar<15>2010 16:26 Aug 03, 2010 Jkt 220001 4,196 collection techniques or other forms of information technology. To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Charles, Hall, RPh, M.S., Chief, Pharmaceutical Management Branch, Cancer Therapy Evaluation Program, National Cancer Institute, Executive Plaza North, Room 7149, 9000 Rockville Pike, Bethesda, Maryland 20891. Or call non-toll-free number 301–496–5725 or e-mail your request, include your address to: hallch@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: PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 Frequency of response 16 Average time per response Annual burden hours 6/60 (0.1) 6,714 Dated: July 28, 2010. Vivian Horovitch-Kelley, NCI Project Clearance Liaison, National Institutes of Health. [FR Doc. 2010–19158 Filed 8–3–10; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; Comment Request; Multi-Ethnic Study of Atherosclerosis (MESA) Event Surveillance 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 SUMMARY: E:\FR\FM\04AUN1.SGM 04AUN1

Agencies

[Federal Register Volume 75, Number 149 (Wednesday, August 4, 2010)]
[Notices]
[Pages 46944-46945]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-19121]


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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: Scholarships for Disadvantaged Students (SDS) Program 
(OMB No. 0915-0149)--Extension

    The Scholarships for Disadvantaged Students (SDS) Program has as 
its purpose, the provision of funds to eligible schools to provide 
scholarships to full-time, financially needy students from 
disadvantaged backgrounds enrolled in health professions and nursing 
programs.
    To qualify for participation in the SDS program, a school must be 
carrying out a program for recruiting and retaining students from 
disadvantaged backgrounds, including students who are members of racial 
and ethnic minority groups (Section 737(d)(1)(B) of the Public Health 
Service (PHS) Act). A school must meet the eligibility criteria to 
demonstrate that the program has achieved success based on the number 
and/or percentage of disadvantaged students who graduate from the 
school. In awarding SDS funds to eligible schools, funding priorities 
must be given to schools based on the proportion of graduating students 
going into primary care, the proportion of underrepresented minority 
students, and the proportion of graduates working in medically 
underserved communities (Section 737(c) of the PHS Act).
    The annual estimate of burden is as follows:

----------------------------------------------------------------------------------------------------------------
                                     Number of     Responses per       Total         Hours per     Total burden
           Instrument               respondents     respondent       responses       response          hours
----------------------------------------------------------------------------------------------------------------
Application.....................             600               1             600              13           7,800

[[Page 46945]]

 
Report..........................             600               1             600               1             600
                                 -------------------------------------------------------------------------------
    Total.......................             600               1             600              14           8,400
----------------------------------------------------------------------------------------------------------------

    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: July 28, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-19121 Filed 8-3-10; 8:45 am]
BILLING CODE 4165-15-P
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