Secretary's Advisory Committee on Human Research Protections, 59264-59265 [2010-24128]

Download as PDF 59264 Federal Register / Vol. 75, No. 186 / Monday, September 27, 2010 / Notices srobinson on DSKHWCL6B1PROD with NOTICES Background Notice is hereby given of the final approval of proposed information collections by the Board of Governors of the Federal Reserve System (Board) under OMB delegated authority, as per 5 CFR 1320.16 (OMB Regulations on Controlling Paperwork Burdens on the Public). Board-approved collections of information are incorporated into the official OMB inventory of currently approved collections of information. Copies of the Paperwork Reduction Act (PRA) Submission, supporting statements and approved collection of information instrument(s) are placed into OMB’s public docket files. The Federal Reserve may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number. FOR FURTHER INFORMATION CONTACT: Federal Reserve Board Clearance Officer—Michelle Shore—Division of Research and Statistics, Board of Governors of the Federal Reserve System, Washington, DC 20551 (202– 452–3829). OMB Desk Officer—Shagufta Ahmed—Office of Information and Regulatory Affairs, Office of Management and Budget, New Executive Office Building, Room 10235, Washington, DC 20503. Final approval under OMB delegated authority of the extension for three years, without revision, of the following report: Report title: Recordkeeping and Disclosure Requirements Associated with Securities Transactions Pursuant to Regulation H. Agency form number: Reg H–3. OMB control number: 7100–0196. Frequency: On occasion. Reporters: State member banks. Estimated annual reporting hours: 97,279 hours. Estimated average hours per response: State member banks (de novo): recordkeeping, 40 hours. State member banks with trust departments: recordkeeping, 2 hours; disclosure, 16 hours. State member banks without trust departments: recordkeeping, 15 minutes; disclosure, 5 hours. Number of respondents: 3 new state member banks (de novo), 224 state member banks with trust departments and state member trust companies, and 621 state member banks without trust departments. General description of report: This information collection is mandatory pursuant the Federal Deposit Insurance VerDate Mar<15>2010 17:01 Sep 24, 2010 Jkt 220001 Corporation Act (12 U.S.C. 325), which authorizes the Federal Reserve to require recordkeeping, disclosure and policy establishment requirements associated with Sections 208.34(c), (d), and (g) of Regulation H, and 15 U.S.C. 78w. If the records maintained by state member banks come into the possession of the Federal Reserve, they are given confidential treatment (5 U.S.C. 552(b)(4), (b)(6), and (b)(8)) under the Freedom of Information Act. Abstract: The Federal Reserve’s Regulation H requires state member banks to maintain records for three years following a securities transaction. These requirements are necessary to protect the customer, to avoid or settle customer disputes, and to protect the institution against potential liability arising under the anti-fraud and insider trading provisions of the Securities Exchange Act of 1934. Current Actions: On July 8, 2010, the Federal Reserve published a notice in the Federal Register (75 FR 39258) seeking public comment for 60 days on the extension, without revision, of the Recordkeeping and Disclosure Requirements Associated with Securities Transactions Pursuant to Regulation H. The comment period for this notice expired on September 7, 2010. The Federal Reserve did not receive any comments. Dated: Board of Governors of the Federal Reserve System, September 21, 2010. Jennifer J. Johnson, Secretary of the Board.. [FR Doc. 2010–24060 Filed 9–24–10; 8:45 am] persons may express their views in writing on the standards enumerated in the BHC Act (12 U.S.C. 1842(c)). If the proposal also involves the acquisition of a nonbanking company, the review also includes whether the acquisition of the nonbanking company complies with the standards in section 4 of the BHC Act (12 U.S.C. 1843). Unless otherwise noted, nonbanking activities will be conducted throughout the United States. Additional information on all bank holding companies may be obtained from the National Information Center website at www.ffiec.gov/nic/. Unless otherwise noted, comments regarding each of these applications must be received at the Reserve Bank indicated or the offices of the Board of Governors not later than October 22, 2010. A. Federal Reserve Bank of Boston (Richard Walker, Community Affairs Officer) P.O. Box 55882, Boston, Massachusetts 02106–2204: 1. Rockville Financial, Rockville, Connecticut; to become a bank holding company by acquiring 100 percent of the voting shares of Rockville Bank, Rockville, Connecticut, in connection with the reorganization of Rockville Financial, MHC, Rockville, Connecticut, from mutual to stock form. Board of Governors of the Federal Reserve System, September 22, 2010. Margaret McCloskey Shanks, Associate Secretary of the Board. [FR Doc. 2010–24150 Filed 9–24–10; 8:45 am] BILLING CODE 6210–01–S BILLING CODE 6210–01–P FEDERAL RESERVE SYSTEM DEPARTMENT OF HEALTH AND HUMAN SERVICES Formations of, Acquisitions by, and Mergers of Bank Holding Companies Secretary’s Advisory Committee on Human Research Protections The companies listed in this notice have applied to the Board for approval, pursuant to the Bank Holding Company Act of 1956 (12 U.S.C. 1841 et seq.) (BHC Act), Regulation Y (12 CFR Part 225), and all other applicable statutes and regulations to become a bank holding company and/or to acquire the assets or the ownership of, control of, or the power to vote shares of a bank or bank holding company and all of the banks and nonbanking companies owned by the bank holding company, including the companies listed below. The applications listed below, as well as other related filings required by the Board, are available for immediate inspection at the Federal Reserve Bank indicated. The applications also will be available for inspection at the offices of the Board of Governors. Interested AGENCY: PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 Department of Health and Human Services, Office of the Secretary, Office of the Assistant Secretary for Health. ACTION: Notice. Pursuant to Section 10(a) of the Federal Advisory Committee Act, U.S.C. Appendix 2, notice is hereby given that the Secretary’s Advisory Committee on Human Research Protections (SACHRP) will hold its twenty-fourth meeting. The meeting will be open to the public. Information about SACHRP and the meeting agenda will be posted on the SACHRP Web site at: https://www.hhs.gov/ohrp/sachrp/ index.html. SUMMARY: The meeting will be held on Tuesday, October 19, 2010, from 8:30 a.m. until 5:15 p.m. and Wednesday, DATES: E:\FR\FM\27SEN1.SGM 27SEN1 srobinson on DSKHWCL6B1PROD with NOTICES Federal Register / Vol. 75, No. 186 / Monday, September 27, 2010 / Notices October 20, 2010, from 8:30 a.m. until 5:15 p.m. ADDRESSES: U.S. Department of Health and Human Services, 200 Independence Avenue SW., Hubert H. Humphrey Building, Room 800, Washington, DC 20201. FOR FUTHER INFORMATION CONTACT: Jerry Menikoff, M.D., J.D., Director, Office for Human Research Protections (OHRP), or Julia Gorey, J.D., Executive Director, SACHRP; U.S. Department of Health and Human Services, 1101 Wootton Parkway, Suite 200, Rockville, Maryland 20852; 240–453–8141; fax: 240–453–6909; e-mail address: Julia.Gorey@hhs.gov. SUPPLEMENTARY INFORMATION: Under the authority of 42 U.S.C. 217a, Section 222 of the Public Health Service Act, as amended, SACHRP was established to provide expert advice and recommendations to the Secretary of Health and Human Services and the Assistant Secretary for Health on issues and topics pertaining to or associated with the protection of human research subjects. On October 19, 2010, SACHRP will hear a panel of four experts discuss the evolving concepts of identifiability and anonymization of data in the context of current and future research. Following the panel, the Subcommittee on Harmonization (SOH) will present a report. The SOH was established by SACHRP at its July 2009 meeting, and is charged with identifying and prioritizing areas in which regulations and/or guidelines for human subjects research adopted by various agencies or offices within HHS would benefit from harmonization, consistency, clarity, simplification and/or coordination. On October 20, 2010, the morning will begin with a panel discussing the use of deception in human subjects research. Subpart A Subcommittee (SAS) will make a report focusing on improvements to the informed consent process. SAS is charged with developing recommendations for consideration by SACHRP about the application of subpart A of 45 CFR part 46 in the current research environment. This subcommittee was established by SACHRP at its October 2006 meeting. Public comment will be heard on both days. Public attendance at the meeting is limited to space available. Individuals who plan to attend the meeting and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the designated contact persons. Members of the public will have the opportunity to provide comments on VerDate Mar<15>2010 17:01 Sep 24, 2010 Jkt 220001 both days of the meeting. Public comment will be limited to five minutes per speaker. Any members of the public who wish to have printed materials distributed to SACHRP members for this scheduled meeting should submit materials to the Executive Director, SACHRP, prior to the close of business Friday, October 15, 2010. Dated: September 21, 2010. Jerry Menikoff, Director, Office for Human Research Protections, Executive Secretary, Secretary’s Advisory Committee on Human Research Protections. [FR Doc. 2010–24128 Filed 9–24–10; 8:45 am] BILLING CODE 4150–36–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60-Day–10–10GY] 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 to provide 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 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 Community Assessment and Engagement Process—New—Division of PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 59265 Health Assessment and Consultation (DHAC), Agency for Toxic Substances and Disease Registry (ATSDR), Centers for Disease Control and Prevention (CDC). Background and Brief Description ATSDR serves the public through responsive public health actions to promote healthy and safe environments and to prevent harmful exposures. To effectively implement ATSDR’s programs, the agency works with communities by listening to and understanding their health concerns and seeking their guidance on where, when, and how to take public health actions. Communities in proximity to hazardous waste sites are concerned that they are being exposed to hazardous substances being released into the environment. Community assessment data will enable ATSDR to determine the perceived needs, concerns, values, and priorities of communities we serve and determine their willingness, interest and ability to participate in community engagement activities. In order to secure this data, ATSDR will interview adult males and females ages 18 and over living near petitioned or National Priorities List sites. ATSDR will also identify health and other concerns and the most effective channels of communication and venues for engagement. ATSDR staff will work with key stakeholders in communities to interview participants. These interviews will take the form of in-depth or telephone interviews with five audiences: General residential population (n = 600), public/private health care providers (n = 200), community leaders (n = 200), elected officials (n = 100), and industry leaders (n = 100). In-depth Interviews will take place at the individual’s residence, at a predetermined interview location, at ATSDR-sponsored town hall meetings, or other ATSDR-sponsored functions. Telephone interviews will take place at the individual’s residence or business location. Findings from these interviews will be used to determine how ATSDR will engage the community in addressing environmental concerns. Interview findings will also help ATSDR reach as many of the members of the affected community as possible and ensure that all community members are given an opportunity to provide input to ATSDR regarding public health assessment and community involvement activities. There are no costs to the respondents other than their time. E:\FR\FM\27SEN1.SGM 27SEN1

Agencies

[Federal Register Volume 75, Number 186 (Monday, September 27, 2010)]
[Notices]
[Pages 59264-59265]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-24128]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES


Secretary's Advisory Committee on Human Research Protections

AGENCY: Department of Health and Human Services, Office of the 
Secretary, Office of the Assistant Secretary for Health.

ACTION: Notice.

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SUMMARY: Pursuant to Section 10(a) of the Federal Advisory Committee 
Act, U.S.C. Appendix 2, notice is hereby given that the Secretary's 
Advisory Committee on Human Research Protections (SACHRP) will hold its 
twenty-fourth meeting. The meeting will be open to the public. 
Information about SACHRP and the meeting agenda will be posted on the 
SACHRP Web site at: https://www.hhs.gov/ohrp/sachrp/.

DATES: The meeting will be held on Tuesday, October 19, 2010, from 8:30 
a.m. until 5:15 p.m. and Wednesday,

[[Page 59265]]

October 20, 2010, from 8:30 a.m. until 5:15 p.m.

ADDRESSES: U.S. Department of Health and Human Services, 200 
Independence Avenue SW., Hubert H. Humphrey Building, Room 800, 
Washington, DC 20201.

FOR FUTHER INFORMATION CONTACT: Jerry Menikoff, M.D., J.D., Director, 
Office for Human Research Protections (OHRP), or Julia Gorey, J.D., 
Executive Director, SACHRP; U.S. Department of Health and Human 
Services, 1101 Wootton Parkway, Suite 200, Rockville, Maryland 20852; 
240-453-8141; fax: 240-453-6909; e-mail address: Julia.Gorey@hhs.gov.

SUPPLEMENTARY INFORMATION: Under the authority of 42 U.S.C. 217a, 
Section 222 of the Public Health Service Act, as amended, SACHRP was 
established to provide expert advice and recommendations to the 
Secretary of Health and Human Services and the Assistant Secretary for 
Health on issues and topics pertaining to or associated with the 
protection of human research subjects.
    On October 19, 2010, SACHRP will hear a panel of four experts 
discuss the evolving concepts of identifiability and anonymization of 
data in the context of current and future research. Following the 
panel, the Subcommittee on Harmonization (SOH) will present a report. 
The SOH was established by SACHRP at its July 2009 meeting, and is 
charged with identifying and prioritizing areas in which regulations 
and/or guidelines for human subjects research adopted by various 
agencies or offices within HHS would benefit from harmonization, 
consistency, clarity, simplification and/or coordination.
    On October 20, 2010, the morning will begin with a panel discussing 
the use of deception in human subjects research. Subpart A Subcommittee 
(SAS) will make a report focusing on improvements to the informed 
consent process. SAS is charged with developing recommendations for 
consideration by SACHRP about the application of subpart A of 45 CFR 
part 46 in the current research environment. This subcommittee was 
established by SACHRP at its October 2006 meeting. Public comment will 
be heard on both days.
    Public attendance at the meeting is limited to space available. 
Individuals who plan to attend the meeting and need special assistance, 
such as sign language interpretation or other reasonable 
accommodations, should notify the designated contact persons. Members 
of the public will have the opportunity to provide comments on both 
days of the meeting. Public comment will be limited to five minutes per 
speaker. Any members of the public who wish to have printed materials 
distributed to SACHRP members for this scheduled meeting should submit 
materials to the Executive Director, SACHRP, prior to the close of 
business Friday, October 15, 2010.

    Dated: September 21, 2010.
Jerry Menikoff,
Director, Office for Human Research Protections, Executive Secretary, 
Secretary's Advisory Committee on Human Research Protections.
[FR Doc. 2010-24128 Filed 9-24-10; 8:45 am]
BILLING CODE 4150-36-P
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