Agency Information Collection Activities; Proposed Collection; Comment Request, 26117-26119 [07-2268]

Download as PDF Federal Register / Vol. 72, No. 88 / Tuesday, May 8, 2007 / Notices cprice-sewell on PROD1PC66 with NOTICES Proposal to approve under OMB delegated authority the extension for three years, without revision, of the following reports: 1. Report title: Report of Selected Balance Sheet Items for Discount Window Borrowers Agency form number: FR 2046 OMB control number: 7100–0289 Frequency: On occasion Reporters: Depository institutions Annual reporting hours: 894 Estimated average hours per response: Primary and Secondary Credit, 0.75 hour; Seasonal Credit, 0.25 hour Number of respondents: 171 General description of report: This information collection is required to obtain or retain a benefit pursuant to section 10B of the Federal Reserve Act [12 U.S.C. § 347b] and is given confidential treatment [5 U.S.C. § 552(b)(4)]. Abstract: The Federal Reserve(s Regulation A, Extensions of Credit by Federal Reserve Banks, requires that the Federal Reserve review balance sheet data in determining whether to extend credit and to help ascertain whether undue use is made of such credit. Borrowers report certain balance sheet data for a period that encompasses the dates of borrowing. There are no proposed changes to the FR 2046; however, the Federal Reserve is clarifying the instructions. 2. Report title: Request for Extension of Time to Dispose of Assets Acquired in Satisfaction of Debts Previously Contracted Agency form number: FR 4006 OMB control number: 7100–0129 Frequency: Annual Reporters: Bank holding companies Annual reporting hours: 180 hours Estimated average hours per response: 5 hours Number of respondents: 36 General description of report: This information collection is required to obtain a benefit pursuant to section 4(c)(2) of the Bank Holding Company Act [12 U.S.C. § 1843(c)(2)] and may be given confidential treatment upon request. The Federal Reserve has established a procedure for requesting an extension in its Regulation Y [12 C.F.R. § 225.22(d)(1)(ii)]. Abstract: A bank holding company that acquired voting securities or assets through foreclosure in the ordinary course of collecting a debt previously contracted may not retain ownership of those shares or assets for more than two years without prior Federal Reserve approval. There is no formal reporting form, and each request for extension must be filed at the appropriate Reserve VerDate Aug<31>2005 15:36 May 07, 2007 Jkt 211001 Bank of the bank holding company. The Federal Reserve uses the information provided in the request to fulfill its statutory obligation to supervise bank holding companies. Board of Governors of the Federal Reserve System, May 3, 2007. Robert deV. Frierson, Deputy Secretary of the Board. [FR Doc. E7–8753 Filed 5–7–07; 8:45 am] BILLING CODE 6210–01–S FEDERAL RESERVE SYSTEM Government in the Sunshine; Meeting Notice Board of Governors of the Federal Reserve System. AGENCY HOLDING THE MEETING: FEDERAL REGISTER CITATION OF PREVIOUS ANNOUNCEMENT: 72 FR 24311, May 2, 2007. PREVIOUSLY ANNOUNCED TIME AND DATE OF THE MEETING: 12 p.m. Monday, May 7, 2007. Change in the time of the closed meeting to 10 a.m., Monday, May 7, 2007. CHANGES IN THE MEETING: FOR MORE INFORMATION PLEASE CONTACT: Michelle Smith, Director, or Dave Skidmore, Assistant to the Board, Office of Board Members at 202–452–2955. SUPPLEMENTARY INFORMATION: You may call 202–452–3206 beginning at approximately 5 p.m. two business days before the meeting for a recorded announcement of bank and bank holding company applications scheduled for the meeting; or you may contact the Board’s Web site at https:// www.federalreserve.gov for an electronic announcement that not only lists applications, but also indicates procedural and other information about the meeting. Dated: May 4, 2007. Robert deV. Frierson, Deputy Secretary of the Board. [FR Doc. 07–2301 Filed 5–4–07; 2:20 pm] BILLING CODE 6210–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency for Healthcare Research and Quality Agency Information Collection Activities; Proposed Collection; Comment Request Agency for Healthcare Research and Quality, Department of Health and Human Services. AGENCY: PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 ACTION: 26117 Notice SUMMARY: This notice announces the intention of the Agency for Healthcare Research and Quality (AHRQ) to request that the Office of Management and Budget (OMB) allow the proposed information collection project: ‘‘Chartering Value Exchanges for Valuedriven Health Care.’’ The information collection will take the form of narrative responses to semiannual Requests for Proposals for participation in a learning network of model multi-stakeholder community health care collaboratives operated to measure, report, and improve the quality and cost of available healthcare. In accordance with the Paperwork Reduction Act of 1995, Public Law 104–13 (44 U.S.C. 3506(c)(2)(A)), AHRQ invites the public to comment on this proposed information collection. DATES: Comments on this notice must be received by July 9, 2007. ADDRESSES: Written comments should be submitted to: Doris Lefkowitz, Reports Clearance Officer, AHRQ, 540 Gaither Road, Room # 5036, Rockville, MD 20850. Copies of the proposed collection plans, application form, and specific details on the estimated burden can be obtained from AHRQ’s Reports Clearance Officer. FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ, Reports Clearance Officer, (301) 427–1477. SUPPLEMENTARY INFORMATION: Proposed Project ‘‘Chartering Value Exchanges for Valuedriven Healthcare’’ This project proposes to twice annually post a public call for parties interested in becoming chartered as Value Exchanges for Value-driven Healthcare, described in the Background Section below. Anticipated benefits of being a chartered Value Exchange include (1) participation in an AHRQmanaged Learning Network and (2) eligibility to request Medicare-inclusive multi-payer patient de-identified individual physician-level performance measurement results. Background The Secretary of Health and Human Services has created and is implementing a Value-driven Healthcare Initiative to enhance person and population-centered care by improving the quality of healthcare services and reducing healthcare costs. Related HHS goals and objectives reflect the President’s Executive Order and encompass (1) promotion of the E:\FR\FM\08MYN1.SGM 08MYN1 cprice-sewell on PROD1PC66 with NOTICES 26118 Federal Register / Vol. 72, No. 88 / Tuesday, May 8, 2007 / Notices establishment of health information technology interoperability standards for exchanging price and quality healthcare data; (2) promotion of the availability and use of transparent, nationally endorsed, consensus-derived quality measures; (3) promotion of the availability and use of transparent, nationally endorsed, consensus-derived measures of price/cost; and, (4) promotion of the use of provider and consumer incentives for high quality and cost efficient healthcare. This Initiative’s design is based on three fundamental principles. The first is that at its core, healthcare is ‘‘local’’— provided in uniquely constituted cultural and market-based environments. As such, improving the value of healthcare requires a critical mass of community stakeholders (public and private purchasers, health plans, providers, and consumers), as well as other relevant community entities (e.g., local information exchange organizations, State data organizations) investing their time and resources toward shared cost and quality improvement goals. We refer to such representative quality improvement community organizations as local multistakeholder collaboratives. Scattered across the country there are community collaboratives in various stages of development ranging from mature multi-stakeholder collaboratives to communities where only a limited number of organizations within a single stakeholder group or a limited number of stakeholder groups are working together. The second principle is that broad access to accurate, meaningful information will improve the value of healthcare services by (1) stimulating provider improvement, (2) engaging consumers in provider selection and treatment choices, and (3) enabling purchasers to align consumer and provider incentives. Generating the information needed to accomplish this is maximized when performance measures can be calculated based on all payer data. The third principle is that establishing a nation-wide learning network will foster market-based healthcare reform. Learning networks are an evidence-based organizational mechanism to achieve rapid identification, dissemination and adoption of best practices. They are comprised of individuals or groups focused on common broad goals. Based on the above, AHRQ plans to establish a nation-wide learning network of mature community-based multi-stakeholder healthcare quality VerDate Aug<31>2005 15:36 May 07, 2007 Jkt 211001 improvement collaboratives. Goals of the Learning Network include facilitating collaborative production of public reports, fostering pay for performance, fostering consumer financial incentives, and ultimately, improving quality. AHRQ will issue semi-annual public Requests for Proposals (RFP) and conduct a selection process immediately thereafter to identify and charter mature multistakeholder collaboratives as Value Exchanges. To be eligible, interested parties must first be recognized by HHS Secretary Michael O. Leavitt as a Community Leader for Value-driven Healthcare. For additional information on Community Leader recognition, see https://www.hhs.gov/transparency/ communities/communityleaders/ communities.html. Method of Collection Each RFP will be posted on the AHRQ public Web site (www.ahrg.gov) with a link to the AHRQ site on the OS transparency Web site as well. The RFP instructions will direct interested parties to electronically submit narrative information (maximum 3000 words) to AHRQ that describes their capacity or plans to develop their capacity to do each of the following: A. Facilitate collection of providerlevel measures across the six performance domains identified by the Institute of Medicine (IOM) (safety, timeliness, effectiveness, efficiency, equitableness, patient-centeredness). B. Use (or promote the use of) transparent, nationally endorsed, consensus-derived performance measures and consumers’ cost for public/consumer reporting. C. Use (or promote the use of) transparent, nationally endorsed, consensus-derived performance measures to reward and foster better performance. D. Use (or promote the use of) transparent, nationally endorsed, consensus-derived performance measures for improvement by directly informing providers of their results. E. Foster collaboration across multiple stakeholders (public and, private purchasers, health plans, providers, and consumers), as well as other relevant community entities (e.g., local information exchange organizations, State data organizations) in the community of interest and serve as a hub for sharing information and dialogue. F. Promote the use of interoperable health information technologies for measurement as appropriate and PO 00000 Frm 00048 Fmt 4703 Sfmt 4703 collaborate with health information sharing processes and in the adoption of these technologies. G. Support knowledge transfer— maintain transparent processes and share lessons learned. H. Conduct ongoing evaluation and improvement of efforts. At a minimum, successful applicants will demonstrate the following: A1. For those conducting or overseeing measurement/auditing and aggregation of data across multiple payers, the ability to do so. A2. For those receiving already aggregated data and calculated performance results from a source (e.g., national aggregators), the ability to effectively implement the use of these results. B. The ability to manage collaborative processes that engage all critical stakeholders. C. Organizational capacity to meet A.1 or A.2 and B above. At a minimum the following organizational characteristics or capacities will be required: • Non-profit status. • Staff/consultant arrangements to provide needed expertise. • History of raising funds or in-kind support uom multiple stakeholders. • Ability to manage collaborative, multi-stakeholder projects and finances. • Ability to track progress in meeting individual collaborative goals, which may include, for example, producing public reports, or fostering pay for performance or consumer incentives. The request for proposals will be open for two months. A review committee will be assembled and have the following composition: • Three experts representing institutional healthcare purchaser stakeholder perspectives. • Three experts representing health plan stakeholder perspectives. • Three experts representing individual consumer stakeholder perspectives. • Three experts representing providers with at least two of the providers being physicians. • AHRQ staff experienced in working with community collaboratives. Proposals will be reviewed by review teams comprised of at least one representative from each stakeholder group listed above and at least one AHRQ staff person. All proposals will be reviewed in the 6 weeks following the closing of the application period. Estimated Annual Respondent Burden E:\FR\FM\08MYN1.SGM 08MYN1 26119 Federal Register / Vol. 72, No. 88 / Tuesday, May 8, 2007 / Notices EXHIBIT 1.—ESTIMATE OF COST BURDEN TO RESPONDENTS Number of estimated respondents Data collection effort Estimated time per respondent in hours Estimated total burden hours Average hourly wage rate Estimated annual cost burden to respondents Draft narrative response to RFP by Collaborative Manager Narrative reviews by 2 members of Collaborative executive committee .................................................................. Narrative revisions by Collaborative Manager ..................... Assembly of narrative with any supporting documents by Collaborative Assistant ..................................................... 50 8 400 $34.67 $13,868 100 50 1 8 100 400 57.90 34.67 5,790 13,868 50 2 100 12.58 1,258 Total .............................................................................. 250 ........................ 1,000 ........................ 34,784 This information collection will not impose a cost burden on the respondent beyond that associated with the above estimates of the time needed to provide the application-requested information, No additional costs to respondents are anticipated, e.g., for capital equipment, software, etc. Estimated Costs to the Federal Government The total cost to the government for its proposal review activity is estimated to be $500,000 annually. cprice-sewell on PROD1PC66 with NOTICES Request for Comments In accordance with the above-cited legislation, comments on the AHRQ’s information collection are requested with regard to any of the following: (a) Whether the proposed collection of information is necessary for the proper performance of health care improvement and information dissemination functions of AHRQ, including whether the information requested will have practical utility; (b) the accuracy of AHRQ’s estimate of burden (including hours and costs) of the proposed collection(s) of information; (c) ways to enhance the quality, utility, and clarity of information to be collected; and, (d) ways to minimize the burden of the collection of information upon the respondents, including the use of automated collection techniques or other forms of information technology. Comments submitted in response to this notice will be summarized and included in the request for OMB approval of the proposed information collection. All comments will become a matter of public record. Dated: May 1, 2007 Carolyn M. Clancy, Director. [FR Doc. 07–2268 Filed 5–7–07: 8:45 am] BILLING CODE 4160–90–M VerDate Aug<31>2005 17:28 May 07, 2007 Jkt 211001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency for Healthcare Research and Quality Notice of Meetings In accordance with section 10(d) of the Federal Advisory Committee Act as amended (5 U.S.C., Appendix 2), the Agency for Healthcare Research and Quality (AHRQ) announces meetings of scientific peer review groups. The subcommittees listed below are part of the Agency’s Health Services Research Initial Review Group Committee. The subcommittee meetings will be closed to the public in accordance with the Federal Advisory Committee Act, section 10(d) of 5 U.S.C., Appendix 2 and 5 U.S.C. 552b(c)(6). Grant applications are to be reviewed and discussed at these meetings. These discussions are likely to involve information concerning individuals associated with the applications, including assessments of their personal qualifications to conduct their proposed projects. This information is exempt from mandatory disclosure under the above-cited statutes. 1. Name of Subcommittee: Health Care Research Training. Date: June 14–15, 2007 (Open from 8 a.m. to 8:15 a.m. on June 14 and closed for reminder of the meeting). Place: Agency for Healthcare Research and Quality (AHRQ), John Eisenberg Conference Center, 540 Gaither Road, Rockville, Maryland 20850. 2. Name of Subcommittee: Health Systems Research. Date: June 14–15, 2007 (Open from 8 a.m. to 8:15 a.m. on June 14 and closed for remainder of the meeting). Place: Agency for Healthcare Research and Quality (AHRQ), John Eisenberg Conference Center, 540 Gaither Road, Rockville, Maryland 20850. 3. Name of Subcommittee: Health Care Quality and Effectiveness Research. Date: June 21–22, 2007 (Open from 8 a.m. to 8:15 a.m. on June 21 and closed for remainder of the meeting). PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 Place: Agency for Healthcare Research and Quality (AHRQ), John Eisenberg Conference Center, 540 Gaither Road, Rockville, Maryland 20850. 4. Name of Subcommittee: Health Care Technology and Decision Sciences. Date: June 28–29, 2007 (Open from 8 a.m. to 8:15 a.m. on June 28 and closed for remainder of the meeting). Place: Agency for Healthcare Research and Quality (AHRQ), John Eisenberg Conference Center, 540 Gaither Road, Rockville, Maryland 20850. Contact Person: Anyone wishing to obtain a roster of members, agenda or minutes of the nonconfidential portions of the meetings should contact Mrs. Bonnie Campbell, Committee Management Officer, Office of Extramural Research, Education and Priority Populations, AHRQ, 540 Gaither Road, Suite 2000, Rockville, Maryland 20850, Telephone (301) 427–1554. Agenda items for these meetings are subject to change as priorities dictate. Dated: April 23, 2007. Carolyn M. Clancy, Director. [FR Doc. 07–2240 Filed 5–7–07; 8:45 am] BILLING CODE 4160–90–M DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency for Toxic Substances and Disease Registry [ATSDR–230] Public Health Assessments and Health Consultations Completed January 2007–March 2007 Agency for Toxic Substances and Disease Registry (ATSDR), Department of Health and Human Services (HHS). ACTION: Notice. AGENCY: SUMMARY: This notice announces those sites for which ATSDR has completed public health assessments and health consultations during the period from January 1, 2007 through March 31, 2007. This list includes sites that are on or proposed for inclusion on the National E:\FR\FM\08MYN1.SGM 08MYN1

Agencies

[Federal Register Volume 72, Number 88 (Tuesday, May 8, 2007)]
[Notices]
[Pages 26117-26119]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-2268]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Agency for Healthcare Research and Quality


Agency Information Collection Activities; Proposed Collection; 
Comment Request

AGENCY: Agency for Healthcare Research and Quality, Department of 
Health and Human Services.

ACTION: Notice

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

SUMMARY: This notice announces the intention of the Agency for 
Healthcare Research and Quality (AHRQ) to request that the Office of 
Management and Budget (OMB) allow the proposed information collection 
project: ``Chartering Value Exchanges for Value-driven Health Care.'' 
The information collection will take the form of narrative responses to 
semiannual Requests for Proposals for participation in a learning 
network of model multi-stakeholder community health care collaboratives 
operated to measure, report, and improve the quality and cost of 
available healthcare. In accordance with the Paperwork Reduction Act of 
1995, Public Law 104-13 (44 U.S.C. 3506(c)(2)(A)), AHRQ invites the 
public to comment on this proposed information collection.

DATES: Comments on this notice must be received by July 9, 2007.

ADDRESSES: Written comments should be submitted to: Doris Lefkowitz, 
Reports Clearance Officer, AHRQ, 540 Gaither Road, Room  5036, 
Rockville, MD 20850.
    Copies of the proposed collection plans, application form, and 
specific details on the estimated burden can be obtained from AHRQ's 
Reports Clearance Officer.

FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ, Reports 
Clearance Officer, (301) 427-1477.

SUPPLEMENTARY INFORMATION:

Proposed Project

``Chartering Value Exchanges for Value-driven Healthcare''

    This project proposes to twice annually post a public call for 
parties interested in becoming chartered as Value Exchanges for Value-
driven Healthcare, described in the Background Section below. 
Anticipated benefits of being a chartered Value Exchange include (1) 
participation in an AHRQ-managed Learning Network and (2) eligibility 
to request Medicare-inclusive multi-payer patient de-identified 
individual physician-level performance measurement results.

Background

    The Secretary of Health and Human Services has created and is 
implementing a Value-driven Healthcare Initiative to enhance person and 
population-centered care by improving the quality of healthcare 
services and reducing healthcare costs. Related HHS goals and 
objectives reflect the President's Executive Order and encompass (1) 
promotion of the

[[Page 26118]]

establishment of health information technology interoperability 
standards for exchanging price and quality healthcare data; (2) 
promotion of the availability and use of transparent, nationally 
endorsed, consensus-derived quality measures; (3) promotion of the 
availability and use of transparent, nationally endorsed, consensus-
derived measures of price/cost; and, (4) promotion of the use of 
provider and consumer incentives for high quality and cost efficient 
healthcare.
    This Initiative's design is based on three fundamental principles. 
The first is that at its core, healthcare is ``local''--provided in 
uniquely constituted cultural and market-based environments. As such, 
improving the value of healthcare requires a critical mass of community 
stakeholders (public and private purchasers, health plans, providers, 
and consumers), as well as other relevant community entities (e.g., 
local information exchange organizations, State data organizations) 
investing their time and resources toward shared cost and quality 
improvement goals. We refer to such representative quality improvement 
community organizations as local multi-stakeholder collaboratives. 
Scattered across the country there are community collaboratives in 
various stages of development ranging from mature multi-stakeholder 
collaboratives to communities where only a limited number of 
organizations within a single stakeholder group or a limited number of 
stakeholder groups are working together.
    The second principle is that broad access to accurate, meaningful 
information will improve the value of healthcare services by (1) 
stimulating provider improvement, (2) engaging consumers in provider 
selection and treatment choices, and (3) enabling purchasers to align 
consumer and provider incentives. Generating the information needed to 
accomplish this is maximized when performance measures can be 
calculated based on all payer data.
    The third principle is that establishing a nation-wide learning 
network will foster market-based healthcare reform. Learning networks 
are an evidence-based organizational mechanism to achieve rapid 
identification, dissemination and adoption of best practices. They are 
comprised of individuals or groups focused on common broad goals.
    Based on the above, AHRQ plans to establish a nation-wide learning 
network of mature community-based multi-stakeholder healthcare quality 
improvement collaboratives. Goals of the Learning Network include 
facilitating collaborative production of public reports, fostering pay 
for performance, fostering consumer financial incentives, and 
ultimately, improving quality. AHRQ will issue semi-annual public 
Requests for Proposals (RFP) and conduct a selection process 
immediately thereafter to identify and charter mature multi-stakeholder 
collaboratives as Value Exchanges. To be eligible, interested parties 
must first be recognized by HHS Secretary Michael O. Leavitt as a 
Community Leader for Value-driven Healthcare.
    For additional information on Community Leader recognition, see 
https://www.hhs.gov/transparency/communities/communityleaders/
communities.html.

Method of Collection

    Each RFP will be posted on the AHRQ public Web site (www.ahrg.gov) 
with a link to the AHRQ site on the OS transparency Web site as well. 
The RFP instructions will direct interested parties to electronically 
submit narrative information (maximum 3000 words) to AHRQ that 
describes their capacity or plans to develop their capacity to do each 
of the following:
    A. Facilitate collection of provider-level measures across the six 
performance domains identified by the Institute of Medicine (IOM) 
(safety, timeliness, effectiveness, efficiency, equitableness, patient-
centeredness).
    B. Use (or promote the use of) transparent, nationally endorsed, 
consensus-derived performance measures and consumers' cost for public/
consumer reporting.
    C. Use (or promote the use of) transparent, nationally endorsed, 
consensus-derived performance measures to reward and foster better 
performance.
    D. Use (or promote the use of) transparent, nationally endorsed, 
consensus-derived performance measures for improvement by directly 
informing providers of their results.
    E. Foster collaboration across multiple stakeholders (public and, 
private purchasers, health plans, providers, and consumers), as well as 
other relevant community entities (e.g., local information exchange 
organizations, State data organizations) in the community of interest 
and serve as a hub for sharing information and dialogue.
    F. Promote the use of interoperable health information technologies 
for measurement as appropriate and collaborate with health information 
sharing processes and in the adoption of these technologies.
    G. Support knowledge transfer--maintain transparent processes and 
share lessons learned.
    H. Conduct ongoing evaluation and improvement of efforts.
    At a minimum, successful applicants will demonstrate the following:
    A1. For those conducting or overseeing measurement/auditing and 
aggregation of data across multiple payers, the ability to do so.
    A2. For those receiving already aggregated data and calculated 
performance results from a source (e.g., national aggregators), the 
ability to effectively implement the use of these results.
    B. The ability to manage collaborative processes that engage all 
critical stakeholders.
    C. Organizational capacity to meet A.1 or A.2 and B above. At a 
minimum the following organizational characteristics or capacities will 
be required:
     Non-profit status.
     Staff/consultant arrangements to provide needed expertise.
     History of raising funds or in-kind support uom multiple 
stakeholders.
     Ability to manage collaborative, multi-stakeholder 
projects and finances.
     Ability to track progress in meeting individual 
collaborative goals, which may include, for example, producing public 
reports, or fostering pay for performance or consumer incentives.
    The request for proposals will be open for two months.
    A review committee will be assembled and have the following 
composition:
     Three experts representing institutional healthcare 
purchaser stakeholder perspectives.
     Three experts representing health plan stakeholder 
perspectives.
     Three experts representing individual consumer stakeholder 
perspectives.
     Three experts representing providers with at least two of 
the providers being physicians.
     AHRQ staff experienced in working with community 
collaboratives.
    Proposals will be reviewed by review teams comprised of at least 
one representative from each stakeholder group listed above and at 
least one AHRQ staff person. All proposals will be reviewed in the 6 
weeks following the closing of the application period.

Estimated Annual Respondent Burden

[[Page 26119]]



                               Exhibit 1.--Estimate of Cost Burden to Respondents
----------------------------------------------------------------------------------------------------------------
                                                                                                     Estimated
                                     Number of    Estimated time     Estimated        Average       annual cost
     Data collection effort          estimated    per respondent   total burden     hourly wage      burden to
                                    respondents      in hours          hours           rate         respondents
----------------------------------------------------------------------------------------------------------------
Draft narrative response to RFP               50               8             400          $34.67         $13,868
 by Collaborative Manager.......
Narrative reviews by 2 members               100               1             100           57.90           5,790
 of Collaborative executive
 committee......................
Narrative revisions by                        50               8             400           34.67          13,868
 Collaborative Manager..........
Assembly of narrative with any                50               2             100           12.58           1,258
 supporting documents by
 Collaborative Assistant........
                                 -------------------------------------------------------------------------------
    Total.......................             250  ..............           1,000  ..............          34,784
----------------------------------------------------------------------------------------------------------------

    This information collection will not impose a cost burden on the 
respondent beyond that associated with the above estimates of the time 
needed to provide the application-requested information, No additional 
costs to respondents are anticipated, e.g., for capital equipment, 
software, etc.

Estimated Costs to the Federal Government

    The total cost to the government for its proposal review activity 
is estimated to be $500,000 annually.

Request for Comments

    In accordance with the above-cited legislation, comments on the 
AHRQ's information collection are requested with regard to any of the 
following: (a) Whether the proposed collection of information is 
necessary for the proper performance of health care improvement and 
information dissemination functions of AHRQ, including whether the 
information requested will have practical utility; (b) the accuracy of 
AHRQ's estimate of burden (including hours and costs) of the proposed 
collection(s) of information; (c) ways to enhance the quality, utility, 
and clarity of information to be collected; and, (d) ways to minimize 
the burden of the collection of information upon the respondents, 
including the use of automated collection techniques or other forms of 
information technology.
    Comments submitted in response to this notice will be summarized 
and included in the request for OMB approval of the proposed 
information collection. All comments will become a matter of public 
record.

    Dated: May 1, 2007
Carolyn M. Clancy,
Director.
[FR Doc. 07-2268 Filed 5-7-07: 8:45 am]
BILLING CODE 4160-90-M
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