Updated OGE Senior Executive Service Performance Review Board, 53250-53251 [E8-21447]

Download as PDF 53250 Federal Register / Vol. 73, No. 179 / Monday, September 15, 2008 / Notices views in writing to the Reserve Bank indicated for that notice or to the offices of the Board of Governors. Comments must be received not later than September 29, 2008. A. Federal Reserve Bank of Atlanta (Steve Foley, Vice President) 1000 Peachtree Street, N.E., Atlanta, Georgia 30309: 1. Leslie D. Ligon, Jr., Clinton, Louisiana; to acquire additional shares of Clinton Bancshares, Inc., and thereby acquire shares of Landmark Bank, both of Clinton, Louisiana. Board of Governors of the Federal Reserve System, September 10, 2008. Robert deV. Frierson, Deputy Secretary of the Board. [FR Doc. E8–21451 Filed 9–12–08; 8:45 am] FEDERAL RESERVE SYSTEM mstockstill on PROD1PC66 with NOTICES Notice of Proposals to Engage in Permissible Nonbanking Activities or to Acquire Companies that are Engaged in Permissible Nonbanking Activities The companies listed in this notice have given notice under section 4 of the Bank Holding Company Act (12 U.S.C. 1843) (BHC Act) and Regulation Y (12 CFR Part 225) to engage de novo, or to acquire or control voting securities or assets of a company, including the companies listed below, that engages either directly or through a subsidiary or other company, in a nonbanking activity that is listed in § 225.28 of Regulation Y (12 CFR 225.28) or that the Board has determined by Order to be closely related to banking and permissible for bank holding companies. Unless otherwise noted, these activities will be conducted throughout the United States. Each notice is available for inspection at the Federal Reserve Bank indicated. The notice also will be available for inspection at the offices of the Board of Governors. Interested persons may express their views in writing on the question whether the proposal complies with the standards of section 4 of the BHC Act. 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 the applications must be received at the Reserve Bank indicated or the offices of the Board of Governors not later than October 10, 2008. A. Federal Reserve Bank of Chicago (Burl Thornton, Assistant Vice President) 230 South LaSalle Street, Chicago, Illinois 60690-1414: 20:22 Sep 12, 2008 Board of Governors of the Federal Reserve System, September 10, 2008. Robert deV. Frierson, Deputy Secretary of the Board. [FR Doc. E8–21452 Filed 9–12–08; 8:45 am] BILLING CODE 6210–01–S GENERAL SERVICES ADMINISTRATION Committee Act (FACA) (Pub. L. 92– 463). The purpose of this subcommittee is to advise GSA in issues pertaining to Service Disabled Veteran Owned Small Businesses (SDVOSB’s) as outlined in Gun number 2 (Advocacy) of GSA’s 21 Gun Salute initiative for SDVOSB’s. Information on the 21 Gun Salute can be found at https://www.gsa.gov/servicedisabled. Please note that nominees who are selected and agree to serve may be asked to complete a financial disclosure form. Dated: September 9, 2008. Michael Rigas, Deputy Associate Administrator, Office of Small Business Utilization, General Services Administration. [FR Doc. E8–21455 Filed 9–12–08; 8:45 am] Office of Small Business Utilization; Small Business Advisory Committee; BILLING CODE 6210–01–S VerDate Aug<31>2005 1. PrivateBancorp, Inc., Chicago, Illinois; to acquire 100 percent of the voting shares of The PrivateWealth Trust Company, a federal savings bank (in organization), Chicago, Illinois, and thereby engage in operating a savings bank pursuant to section 225.28(b)(4)(ii) of Regulation Y. Jkt 214001 BILLING CODE 6820–34–S Notice of Request for Nominations for Subcommittee on Service Disabled Veteran Owned Small Business (SDVOSB), GSA Small Business Advisory Committee OFFICE OF GOVERNMENT ETHICS Office of Small Business Utilization, GSA. ACTION: Notice. (OGE). AGENCY: The General Services Administration (GSA) is requesting the public to submit nominations of individuals for the Service Disabled Veteran Owned Small Business Subcommittee of the GSA Small Business Advisory Committee as a part of GSA’s initiative to meet and exceed its three percent contracting goal for Service-Disabled Veteran-Owned Small Businesses. DATES: Interested parties should submit the nomination form on or before September 30, 2008. ADDRESSES: The nomination form is available at https://www.gsa.gov/servicedisabled and should be submitted to sbac@gsa.gov. When submitting a nomination via email, please put ‘‘SDVOSB Subcommittee nomination’’ in the subject line. Nominations may also be sent by mail to: General Services Administration, Small Business Advisory Committee, 1800 F Street NW, Room 6029, Washington, DC 20405. Those wishing to send the nominations by fax may do so using (202) 501–2590. SUMMARY: FOR FURTHER INFORMATION CONTACT Aaron Collmann, Room 6029, GSA Building, 1800 F Street, NW., Washington, DC 20405 (202) 501–1021 or email at sbac@gsa.gov. SUPPLEMENTARY INFORMATION: This notice is published in accordance with the provisions of the Federal Advisory PO 00000 Frm 00063 Fmt 4703 Sfmt 4703 Updated OGE Senior Executive Service Performance Review Board AGENCY: ACTION: Office of Government Ethics Notice. SUMMARY: Notice is hereby given of the appointment of the members of the updated OGE Senior Executive Service (SES) Performance Review Board. DATES: Effective Date: September 15, 2008. FOR FURTHER INFORMATION CONTACT: Joseph E. Gangloff, Deputy Director for Agency Programs, Office of Government Ethics, Suite 500, 1201 New York Avenue, NW., Washington, DC 20005– 3917; Telephone: 202–482–9300; TDD: 202–482–9293; FAX: 202–482–9238. SUPPLEMENTARY INFORMATION: 5 U.S.C. 4314(c) requires each agency to establish, in accordance with regulations prescribed by the Office of Personnel Management at 5 CFR part 430, subpart C and § 430.310 thereof in particular, one or more Senior Executive Service performance review boards. As a small executive branch agency, OGE has just one board. In order to ensure an adequate level of staffing and to avoid a constant series of recusals, the designated members of OGE’s SES Performance Review Board are being drawn, as in the past, in large measure from the ranks of other agencies. The board shall review and evaluate the initial appraisal of each OGE senior executive’s performance by his or her supervisor, along with any recommendations in each instance to the appointing authority relative to the performance of the senior executive. This notice updates the membership of E:\FR\FM\15SEN1.SGM 15SEN1 Federal Register / Vol. 73, No. 179 / Monday, September 15, 2008 / Notices OGE’s SES Performance Review Board as it was most recently published at 72 FR 54666–54667 (September 26, 2007). Approved: September 9, 2008. Robert I. Cusick, Director, Office of Government Ethics. The following officials have been appointed as regular members of the SES Performance Review Board of the Office of Government Ethics: Joseph E. Gangloff [Chair], Deputy Director for Agency Programs, Office of Government Ethics; Don W. Fox [Alternate Chair], General Counsel, Office of Government Ethics; Daniel L. Koffsky, Special Counsel, Office of Legal Counsel, Department of Justice; David Maggi, Chief, Ethics Law and Programs Division, Office of the Assistant General Counsel for Administration, Department of Commerce; and Robert A. Shapiro, Associate Solicitor for Legal Counsel, Department of Labor. [FR Doc. E8–21447 Filed 9–12–08; 8:45 am] BILLING CODE 6345–02–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2007–D–0434] (formerly Docket No. 2007D–0386) Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application AGENCY: Food and Drug Administration, HHS. mstockstill on PROD1PC66 with NOTICES ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. DATES: Fax written comments on the collection of information by October 15, 2008. ADDRESSES: To ensure that comments on the information collection are received, VerDate Aug<31>2005 20:22 Sep 12, 2008 Jkt 214001 OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: 202–395–6974, or e-mailed to baguilar@omb.eop.gov. All comments should be identified with the OMB control number 0910–NEW and title ‘‘Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application.’’ Also include the FDA docket number found in brackets in the heading of this document. FOR FURTHER INFORMATION CONTACT: Elizabeth Berbakos, Office of Information Management (HFA–710), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301–796–3792. SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application Public Law 109–462, the Dietary Supplement and Nonprescription Drug Consumer Protection Act, amended the Federal Food, Drug, and Cosmetic Act (the act) to add safety reporting requirements for nonprescription drug products that are marketed without an approved application. In accordance with section 760(b) of the act (21 U.S.C. 379aa), the manufacturer, packer, or distributor whose name appears on the label of a nonprescription drug marketed in the United States without an approved application (referred to as the responsible person) must submit to FDA any report of a serious adverse event associated with such drug when used in the United States, accompanied by a copy of the label on or within the retail package of such drug. In addition, the responsible person must submit followup reports of new medical information related to a submitted serious adverse event report that is received within 1 year of the initial report (section 760(c)(2) of the act). Section 760(e) of the act also requires that responsible persons maintain records of nonprescription drug adverse event reports, whether or not the event PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 53251 is serious, for a period of 6 years. The guidance document provides information on: (1) The minimum data elements that should be included in a serious adverse event report, (2) the label that should be included with the report, (3) reporting formats for paper and electronic submissions, and (4) how and where to submit the reports. Title: Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application. Description of Respondents: Respondents to this collection of information are manufacturers, packers, or distributors whose name appears on the label of a nonprescription drug marketed in the United States without an approved application. Burden Estimate: FDA is requesting public comment on estimates of the number of annual submissions from these respondents and recordkeeping, as required by Public Law 109–462 and described in the guidance ‘‘Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application.’’ The estimates for annual reporting and recordkeeping are based on FDA’s knowledge of adverse drug experience reports historically submitted annually for prescription drug products and for nonprescription drug products marketed under an approved application, including knowledge about the time needed to prepare the reports and to maintain records. FDA receives approximately 2,500 serious adverse event reports for nonprescription drug products marketed under approved applications, which comprise approximately 20 percent of the overall nonprescription drug market. Based on this data, we estimate between 10,000 and 15,000 (i.e., 12,500) total annual responses from approximately 50 respondents for nonprescription drugs marketed without an approved application, and that each submission will take approximately 2 hours to prepare and submit to FDA. In the Federal Register of October 15, 2007 (72 FR 58316), FDA published a 60-day notice requesting public comment on the information collection provisions. No comments were received on the information collection. FDA estimates the burden of this collection of information as follows: E:\FR\FM\15SEN1.SGM 15SEN1

Agencies

[Federal Register Volume 73, Number 179 (Monday, September 15, 2008)]
[Notices]
[Pages 53250-53251]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-21447]


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OFFICE OF GOVERNMENT ETHICS


Updated OGE Senior Executive Service Performance Review Board

AGENCY: Office of Government Ethics (OGE).

ACTION: Notice.

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

SUMMARY: Notice is hereby given of the appointment of the members of 
the updated OGE Senior Executive Service (SES) Performance Review 
Board.

DATES: Effective Date: September 15, 2008.

FOR FURTHER INFORMATION CONTACT: Joseph E. Gangloff, Deputy Director 
for Agency Programs, Office of Government Ethics, Suite 500, 1201 New 
York Avenue, NW., Washington, DC 20005-3917; Telephone: 202-482-9300; 
TDD: 202-482-9293; FAX: 202-482-9238.

SUPPLEMENTARY INFORMATION: 5 U.S.C. 4314(c) requires each agency to 
establish, in accordance with regulations prescribed by the Office of 
Personnel Management at 5 CFR part 430, subpart C and Sec.  430.310 
thereof in particular, one or more Senior Executive Service performance 
review boards. As a small executive branch agency, OGE has just one 
board. In order to ensure an adequate level of staffing and to avoid a 
constant series of recusals, the designated members of OGE's SES 
Performance Review Board are being drawn, as in the past, in large 
measure from the ranks of other agencies. The board shall review and 
evaluate the initial appraisal of each OGE senior executive's 
performance by his or her supervisor, along with any recommendations in 
each instance to the appointing authority relative to the performance 
of the senior executive. This notice updates the membership of

[[Page 53251]]

OGE's SES Performance Review Board as it was most recently published at 
72 FR 54666-54667 (September 26, 2007).

    Approved: September 9, 2008.
Robert I. Cusick,
Director, Office of Government Ethics.
    The following officials have been appointed as regular members of 
the SES Performance Review Board of the Office of Government Ethics:

Joseph E. Gangloff [Chair], Deputy Director for Agency Programs, Office 
of Government Ethics;
Don W. Fox [Alternate Chair], General Counsel, Office of Government 
Ethics;
Daniel L. Koffsky, Special Counsel, Office of Legal Counsel, Department 
of Justice;
David Maggi, Chief, Ethics Law and Programs Division, Office of the 
Assistant General Counsel for Administration, Department of Commerce; 
and
Robert A. Shapiro, Associate Solicitor for Legal Counsel, Department of 
Labor.

[FR Doc. E8-21447 Filed 9-12-08; 8:45 am]
BILLING CODE 6345-02-P

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