Proposed Data Collections Submitted for Public Comment and Recommendations, 41079-41080 [E7-14439]

Download as PDF 41079 Federal Register / Vol. 72, No. 143 / Thursday, July 26, 2007 / Notices ESTIMATE OF ANNUALIZED BURDEN HOURS—Continued Average number of responses per respondent Number of respondents Form Average burden per response (in hours) Total burden hours High Risk Inpatient Influenza Vaccine—Summary Form Method A ............... High Risk Inpatient Influenza Vaccine-Numerator Data Form Method B ....... High Risk Inpatient Influenza Vaccine—Summary Form Method B ............... High Risk Inpatient Influenza Vaccine—Denominator Data Form Method B Laboratory Identified MDRO Event—Summary Form ..................................... Long-term Acute Care Hospital Survey ........................................................... 1,500 500 500 500 1,500 75 5 250 5 250 3 1 16 10/60 4 5/60 1 30/60 120,000 20,833 10,000 10,417 4,500 38 Total .......................................................................................................... ........................ ........................ ........................ 1,276,153 Dated: July 19, 2007. Maryam I. Daneshvar, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E7–14432 Filed 7–25–07; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–07–0106] rwilkins on PROD1PC63 with NOTICES Proposed Data Collections Submitted for Public Comment and Recommendations 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 Centers for Disease Control and Prevention (CDC) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a copy of the data collection plans and instruments, call 404–639–5960 and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance Officer, 1600 Clifton Road, MS–D74, Atlanta, GA 30333 or send an e-mail to omb@cdc.gov. Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Written comments should VerDate Aug<31>2005 17:41 Jul 25, 2007 Jkt 211001 be received within 60 days of this notice. Proposed Project Preventive Health and Health Services Block Grant, Annual Application and Reports—Revision—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description In 1994, OMB approved the collection of information provided in the grant applications and annual reports for the Preventive Health and Health Services Block Grant (OMB #0920–0106). This approval expires on October 31, 2008. * * * CDC is requesting OMB clearance for this legislatively mandated information collection until January 31, 2011. The request is to approve the development and adherence to Healthy People 2010, the Nation’s Health Objectives which was released the Spring of 2000. The PHHS block grant is mandated according to section 1904 to adhere to the Healthy People framework, therefore, the current application and report format was restructured to coincide with 2010. This information collected through the applications from the official State health agencies is required from section 1905 of the Public Health Service Act. The information collected from the annual reports is required by section 1906. * * * The data collection tool is being moved from software that is installed to each user’s desktop to a web-based system. The following changes will be incorporated into the web-based system: (1) Applications are referred to as Work Plans, (2) Grantees are asked to submit Work Plans within recommended page ranges based on the amount of funding with the objective of reducing the number of pages submitted per grantee, (3) Review functions have been added to the Work Plan, Success Stories, and Annual Report sections, (4) The rationale that was used by the Preventive Health and Health Services PO 00000 Frm 00031 Fmt 4703 Sfmt 4703 Block Grant (PHHSBG) Advisory Committee to prioritize use of PHHSBG funds is identified via check boxes versus a free form text field, (5) Information is captured relative to the percent of time dedicated to the PHHSBG by the Block Grant Coordinator and other Full Time Equivalents (FTEs) that are paid for in whole or in part with Block Grant dollars, (6) Grantees select the Evidence Based Guideline or Best Practice that is used as the basis for interventions from a pre-defined list, (7) Grantees select the CDC Goals that are being addressed with Block Grant Funds from a pre-defined list and identify the location wherein the funds are being applied, (8) Information items are broken down into discrete fields, for example, specific begin and end dates are entered for objectives and activities, and the components for a SMART (Specific Measurable Achievable, Realistic and Time based) objective are entered individually versus via free form text fields, (9) Grantees select a percent from a pre-defined list in the Annual Report section to identify the extent to which objectives and activities have been accomplished. Written detail is provided only for those items that are ‘exceptions’ to projected outcomes, (10) A Compliance Review section has been added to provide grantees with general information regarding the Compliance Review process and specific information that pertains to past reviews of their state/territory/tribe. The total burden hours is estimated at 3355 hours, a reduction of 915 hours below the previous data collection estimate (4270). The number of hours is equal to 61 grantees × 25 hours (1525 hrs) for completion of the application and 61 grantees × 30 hours (1830 hrs) for completion of the annual report. Respondent burden is based upon experience with the Grant Application and Reporting system that is used to complete applications and annual reports. E:\FR\FM\26JYN1.SGM 26JYN1 41080 Federal Register / Vol. 72, No. 143 / Thursday, July 26, 2007 / Notices There are no costs to respondents except their time to participate in the survey. ESTIMATED ANNUALIZED BURDEN HOURS Number of responses per respondent Number of respondents Average burden per response (in hrs.) Total burden (in hours) Respondents Form name Grantees ........................................... Annual Application ........................... Annual Report .................................. 61 61 1 1 25 30 1525 1830 Total ........................................... ........................................................... ........................ ........................ ........................ 3355 Dated: July 20, 2007. Maryam I. Daneshvar, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E7–14439 Filed 7–25–07; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Advisory Committee for Injury Prevention and Control (ACIPC), Science and Program Review Subcommittee rwilkins on PROD1PC63 with NOTICES In accordance with Section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), the Centers for Disease Control and Prevention (CDC) announces, the following meeting for the aforementioned committee and subcommittee: Name: Science and Program Review Subcommittee (SPRS). Times and Date: 11:30 a.m.–11:35 a.m., August 20, 2007 (Open). 11:35 a.m.–12:30 p.m., August 20, 2007 (Closed). Place: CDC, Koger Center, Vanderbilt Building, Room 1006, 2939 Flowers Road, Atlanta, Georgia 30341–3724. Purpose: The subcommittee provides advice on the needs, structure, progress, and performance of programs in the National Center for Injury Prevention and Control (NCIPC). Matters To Be Discussed: The subcommittee will have a secondary review, discussion, and evaluation on the individual research grant and cooperative agreement applications submitted in response to the two Fiscal Year 2007 Requests for Applications (RFAs) related to the following individual research announcements: RFA–CE–05–020, Youth Violence Prevention through Community-Level Change; and RFA–CE–07– 011, Multi-Level Parent Training Effectiveness Trial—Phase II (U49). Following this meeting, the voting members of ACIPC will meet via teleconference to vote on the recommendations of the SPRS regarding the RFAs. VerDate Aug<31>2005 16:36 Jul 25, 2007 Jkt 211001 Name: Advisory Committee for Injury Prevention and Control. Times and Date: 12:30 p.m.–12:55 p.m., August 20, 2007 (Open). 12:55 p.m.–1:30 p.m., August 20, 2007 (Closed). Place: CDC, Koger Center, Vanderbilt Building, Room 1006, 2939 Flowers Road, Atlanta, Georgia 30341–3724. Purpose: The committee advises and makes recommendations to the Secretary, Department of Health and Human Services, the Director, CDC, and the Director, NCIPC regarding feasible goals for the prevention and control of injury. The committee makes recommendations regarding policies, strategies, objectives, and priorities, and reviews progress toward injury prevention and control. Matters To Be Discussed: Agenda items for the open portion include the call to order and introductions and request for public comments. The committee will vote on the results of the secondary review. This portion of the meeting will be closed to the public in accordance with the provisions set forth in section 552b(c)(4) and (b), title 5 U.S.C., and the Determination of the Acting Director, Management Analysis and Services Office, CDC pursuant to Public Law 92–463. Agenda items are subject to change as priorities dictate. For Further Information Contact: Ms. Amy Harris, Executive Secretary, ACIPC, NCIPC, CDC, 4770 Buford Highway, NE., M/S K61, Atlanta, Georgia 30341–3724, Telephone (770) 488–4936. The Director, Management Analysis and Services Office, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both CDC and the Agency for Toxic Substances and Disease Registry. Dated: July 17, 2007. Elaine L. Baker, Acting Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. E7–14430 Filed 7–25–07; 8:45 am] BILLING CODE 4163–18–P PO 00000 Frm 00032 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 2007D–0290] Draft Guidance for Industry: Cell Selection Devices for Point of Care Production of Minimally Manipulated Autologous Peripheral Blood Stem Cells; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing the availability of a draft document entitled ‘‘Guidance for Industry: Cell Selection Devices for Point of Care Production of Minimally Manipulated Autologous Peripheral Blood Stem Cells (PBSCs)’’ dated July 2007. The draft guidance document discusses certain cell selection devices that minimally manipulate autologous PBSCs at the point of care for specific clinical indications, and the applicability of the requirements to such PBSCs. The guidance also discusses the submission of data intended to support approval of cell selection devices. DATES: Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the agency considers your comment on this draft guidance before it begins work on the final version of the guidance submit written or electronic comments on the draft guidance by October 24, 2007. ADDRESSES: Submit written requests for single copies of the draft guidance to the Office of Communication, Training, and Manufacturers Assistance (HFM–40), Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, 1401 Rockville Pike, suite 200N, Rockville, MD 20852–1448. Send one self-addressed adhesive label to assist the office in processing your requests. The draft guidance may also be obtained by mail by calling CBER at 1– E:\FR\FM\26JYN1.SGM 26JYN1

Agencies

[Federal Register Volume 72, Number 143 (Thursday, July 26, 2007)]
[Notices]
[Pages 41079-41080]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-14439]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-07-0106]


Proposed Data Collections Submitted for Public Comment and 
Recommendations

    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 Centers for Disease Control and 
Prevention (CDC) will publish periodic summaries of proposed projects. 
To request more information on the proposed projects or to obtain a 
copy of the data collection plans and instruments, call 404-639-5960 
and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance 
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail 
to omb@cdc.gov.
    Comments are invited on: (a) Whether the proposed collection of 
information is necessary for the proper performance of the functions of 
the agency, including whether the information shall have practical 
utility; (b) the accuracy of the agency's estimate of the burden of the 
proposed collection of information; (c) ways to enhance the quality, 
utility, and clarity of the information to be collected; and (d) ways 
to minimize the burden of the collection of information on respondents, 
including through the use of automated collection techniques or other 
forms of information technology. Written comments should be received 
within 60 days of this notice.

Proposed Project

    Preventive Health and Health Services Block Grant, Annual 
Application and Reports--Revision--National Center for Chronic Disease 
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control 
and Prevention (CDC).

Background and Brief Description

    In 1994, OMB approved the collection of information provided in the 
grant applications and annual reports for the Preventive Health and 
Health Services Block Grant (OMB 0920-0106). This approval 
expires on October 31, 2008. * * * CDC is requesting OMB clearance for 
this legislatively mandated information collection until January 31, 
2011. The request is to approve the development and adherence to 
Healthy People 2010, the Nation's Health Objectives which was released 
the Spring of 2000. The PHHS block grant is mandated according to 
section 1904 to adhere to the Healthy People framework, therefore, the 
current application and report format was restructured to coincide with 
2010.
    This information collected through the applications from the 
official State health agencies is required from section 1905 of the 
Public Health Service Act. The information collected from the annual 
reports is required by section 1906. * * * The data collection tool is 
being moved from software that is installed to each user's desktop to a 
web-based system. The following changes will be incorporated into the 
web-based system: (1) Applications are referred to as Work Plans, (2) 
Grantees are asked to submit Work Plans within recommended page ranges 
based on the amount of funding with the objective of reducing the 
number of pages submitted per grantee, (3) Review functions have been 
added to the Work Plan, Success Stories, and Annual Report sections, 
(4) The rationale that was used by the Preventive Health and Health 
Services Block Grant (PHHSBG) Advisory Committee to prioritize use of 
PHHSBG funds is identified via check boxes versus a free form text 
field, (5) Information is captured relative to the percent of time 
dedicated to the PHHSBG by the Block Grant Coordinator and other Full 
Time Equivalents (FTEs) that are paid for in whole or in part with 
Block Grant dollars, (6) Grantees select the Evidence Based Guideline 
or Best Practice that is used as the basis for interventions from a 
pre-defined list, (7) Grantees select the CDC Goals that are being 
addressed with Block Grant Funds from a pre-defined list and identify 
the location wherein the funds are being applied, (8) Information items 
are broken down into discrete fields, for example, specific begin and 
end dates are entered for objectives and activities, and the components 
for a SMART (Specific Measurable Achievable, Realistic and Time based) 
objective are entered individually versus via free form text fields, 
(9) Grantees select a percent from a pre-defined list in the Annual 
Report section to identify the extent to which objectives and 
activities have been accomplished. Written detail is provided only for 
those items that are `exceptions' to projected outcomes, (10) A 
Compliance Review section has been added to provide grantees with 
general information regarding the Compliance Review process and 
specific information that pertains to past reviews of their state/
territory/tribe.
    The total burden hours is estimated at 3355 hours, a reduction of 
915 hours below the previous data collection estimate (4270). The 
number of hours is equal to 61 grantees x 25 hours (1525 hrs) for 
completion of the application and 61 grantees x 30 hours (1830 hrs) for 
completion of the annual report. Respondent burden is based upon 
experience with the Grant Application and Reporting system that is used 
to complete applications and annual reports.

[[Page 41080]]

    There are no costs to respondents except their time to participate 
in the survey.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
          Respondents               Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent       (in hrs.)      (in hours)
----------------------------------------------------------------------------------------------------------------
Grantees......................  Annual                        61               1              25            1525
                                 Application.
                                Annual Report...              61               1              30            1830
                               ---------------------------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............            3355
----------------------------------------------------------------------------------------------------------------


    Dated: July 20, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and 
Prevention.
 [FR Doc. E7-14439 Filed 7-25-07; 8:45 am]
BILLING CODE 4163-18-P
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