Bureau of International Labor Affairs: Labor Advisory Committee for Trade Negotiations and Trade Policy, 9615-9616 [2010-4352]

Download as PDF Federal Register / Vol. 75, No. 41 / Wednesday, March 3, 2010 / Notices DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated October 16, 2009, and published in the Federal Register on October 28, 2009, (74 FR 55587), American Radiolabeled Chemical, Inc., 101 Arc Drive, St. Louis, Missouri 63146, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II: Drug mstockstill on DSKH9S0YB1PROD with NOTICES [FR Doc. 2010–4403 Filed 3–2–10; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE I I I I I I I I II II II II II II II II II II II II II II II II II II II II II The company plans to manufacture small quantities of the listed controlled substances as radiolabeled compounds for biochemical research. No comments or objections have been received. DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of American Radiolabeled Chemical, Inc. to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated American Radiolabeled Chemical Inc. to ensure that the company’s registration is consistent with the public interest. The investigation has included inspection and testing of the company’s physical 16:08 Mar 02, 2010 Dated: February 24, 2010. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. Schedule Gamma Hydroxybutyric Acid (2010) ........................................ Ibogaine (7260) ............................ Lysergic acid diethylamide (7315) Tetrahydrocannabinols (7370) ...... Dimethyltryptamine (7435) ........... 1-[1-(2– Thienyl)cyclohexyl]piperidine (7470) ........................................ Dihydromorphine (9145) ............... Normorphine (9313) ..................... Amphetamine (1100) .................... Methamphetamine (1105) ............ Amobarbital (2125) ....................... Phencyclidine (7471) .................... Phenylacetone (8501) .................. Cocaine (9041) ............................. Codeine (9050) ............................. Dihydrocodeine (9120) ................. Oxycodone (9143) ........................ Hydromorphone (9150) ................ Ecgonine (9180) ........................... Hydrocodone (9193) ..................... Meperidine (9230) ........................ Metazocine (9240) ........................ Dextropropoxyphene, bulk (nondosage forms) (9273) ............... Morphine (9300) ........................... Oripavine (9330) ........................... Thebaine (9333) ........................... Oxymorphone (9652) .................... Phenazocine (9715) ..................... Fentanyl (9801) ............................ VerDate Nov<24>2008 security systems, verification of the company’s compliance with state and local laws, and a review of the company’s background and history. Therefore, pursuant to 21 U.S.C. 823, and in accordance with 21 CFR 1301.33, the above named company is granted registration as a bulk manufacturer of the basic classes of controlled substances listed. Jkt 220001 Drug Enforcement Administration Manufacturer of Controlled Substances Notice of Registration By Notice dated October 21, 2009, and published in the Federal Register on October 28, 2009, (74 FR 55588), Johnson Matthey Inc., Custom Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New Jersey 08066–1742, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II: Drug Frm 00044 Fmt 4703 The company plans to manufacture the listed controlled substances in bulk for sale to its customers. No comments or objections have been received. DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Johnson Matthey Inc. to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Johnson Matthey Inc. to ensure that the company’s registration is consistent with the public interest. The investigation has included inspection and testing of the company’s physical security systems, verification of the company’s compliance with state and local laws, and a review of the company’s background and history. Therefore, pursuant to 21 U.S.C. 823, and in accordance with 21 CFR 1301.33, the above named company is granted registration as a bulk manufacturer of the basic classes of controlled substances listed. Dated: February 24, 2010. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2010–4404 Filed 3–2–10; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF LABOR Office of the Secretary Schedule Gamma Hydroxybutyric Acid (2010) ........................................ Tetrahydrocannabinols (7370) ...... Dihydromorphine (9145) ............... Difenoxin (9168) ........................... Propiram (9649) ............................ Amphetamine (1100) .................... Methamphetamine (1105) ............ Lisdexamfetamine (1205) ............. Methylphenidate (1724) ................ Nabilone (7379) ............................ Cocaine (9041) ............................. Codeine (9050) ............................. Dihydrocodeine (9120) ................. Oxycodone (9143) ........................ Hydromorphone (9150) ................ Ecgonine (9180) ........................... Hydrocodone (9193) ..................... Meperidine (9230) ........................ Methadone (9250) ........................ Methadone intermediate (9254) ... Morphine (9300) ........................... Thebaine (9333) ........................... Oxymorphone (9652) .................... Noroxymorphone (9668) ............... Alfentanil (9737) ........................... Remifentanil (9739) ...................... Sufentanil (9740) .......................... Fentanyl (9801) ............................ PO 00000 9615 Sfmt 4703 Bureau of International Labor Affairs: Labor Advisory Committee for Trade I Negotiations and Trade Policy I I I I II II II II II II II II II II II II II II II II II II II II II II II ACTION: Meeting Notice. SUMMARY: Pursuant to the provisions of the Federal Advisory Committee Act (Pub. L. 92–463, as amended), notice is hereby given of a meeting of the Labor Advisory Committee for Trade Negotiation and Trade Policy. Date, Time, Place: March 16, 2010; 10:30 a.m.–11:30 a.m.; U.S. Department of Labor, Secretary’s Conference Room, 200 Constitution Ave., NW., Washington, DC. Purpose: The meeting will include a review and discussion of current issues which influence U.S. trade policy. Potential U.S. negotiating objectives and bargaining positions in current and anticipated trade negotiations will be discussed. Pursuant to 19 U.S.C. 2155(f) it has been determined that the meeting will be concerned with matters the disclosure of which would seriously compromise the Government’s negotiating objectives or bargaining E:\FR\FM\03MRN1.SGM 03MRN1 9616 Federal Register / Vol. 75, No. 41 / Wednesday, March 3, 2010 / Notices positions. Accordingly, the meeting will be closed to the public. FOR FURTHER INFORMATION CONTACT: Gregory Schoepfle, Director, Office of Trade and Labor Affairs; Phone: (202) 693–4887. Signed at Washington, DC, the 25th day of February 2010. Sandra Polaski, Deputy Undersecretary, International Affairs. [FR Doc. 2010–4352 Filed 3–2–10; 8:45 am] BILLING CODE 4510–28–P NATIONAL SCIENCE FOUNDATION Committee Management Renewals The NSF management officials having responsibility for three advisory committees listed below have determined that renewing these groups for another two years is necessary and in the public interest in connection with the performance of duties imposed upon the Director, National Science Foundation (NSF), by 42 U.S.C. 1861 et seq. This determination follows consultation with the Committee Management Secretariat, General Services Administration. Committees: Advisory Committee for Environmental Research and Education, #9487. Proposal Review Panel for Industrial Innovations and Partnerships, #28164. Proposal Review Panel for Emerging Frontiers in Research and Innovation, #34558. Effective date for renewal is March 1, 2010. For more information, please contact Susanne Bolton, NSF, at (703) 292–7488. Susanne Bolton, Committee Management Officer. [FR Doc. 2010–4233 Filed 3–2–10; 8:45 am] BILLING CODE 7555–01–P NUCLEAR REGULATORY COMMISSION mstockstill on DSKH9S0YB1PROD with NOTICES [Docket Nos. 50–266 and 50–301; NRC– 2010–0078] FPL Energy Point Beach, LLC; Notice of Consideration of Issuance of Amendment to Facility Operating License, Proposed No Significant Hazards Consideration Determination, and Opportunity for a Hearing The U.S. Nuclear Regulatory Commission (the Commission) is considering issuance of an amendment to Renewed Facility Operating License Nos. DPR–24 and DPR–27 issued to FPL Energy Point Beach, LLC (the licensee) VerDate Nov<24>2008 16:08 Mar 02, 2010 Jkt 220001 for operation of the Point Beach Nuclear Plant, Units 1 and 2 located in the Town of Two Creeks, Manitowoc County, Wisconsin. On July 14, 2009, the Nuclear Regulatory Commission published a Notice of Consideration of Issuance, Proposed No Significant Hazards Consideration Determination, and Opportunity for Hearing in the Federal Register (74 FR 34048) for a proposed amendment that would change the legal name of the licensee and owner from ‘‘FPL Energy Point Beach, LLC’’ to ‘‘NextEra Energy Point Beach, LLC.’’ On January 19, 2010, the licensee submitted a supplement which expanded the original scope of work. The proposed revisions would correct an administrative error within a License Condition contained in Appendix C of the Renewed Facility Operating Licenses. The correction changes ‘‘FPLE Group Capital’’ to the appropriately titled ‘‘FPL Group Capital.’’ Before issuance of the proposed license amendment, the Commission will have made findings required by the Atomic Energy Act of 1954, as amended (the Act), and the Commission’s regulations. The Commission has made a proposed determination that the amendment request involves no significant hazards consideration. Under the Commission’s regulations in Title 10 of the Code of Federal Regulations (10 CFR), Section 50.92, this means that operation of the facility in accordance with the proposed amendment would not (1) involve a significant increase in the probability or consequences of an accident previously evaluated; or (2) create the possibility of a new or different kind of accident from any accident previously evaluated; or (3) involve a significant reduction in a margin of safety. As required by 10 CFR 50.91(a), the licensee has provided its analysis of the issue of no significant hazards consideration, which is presented below: 1. Does the proposed amendment involve a significant increase in the probability or consequences of an accident previously evaluated? Response: No. This request is for administrative changes only. No actual facility equipment or accident analyses will be affected by the proposed changes. Therefore, this request will have no impact on the probability or consequences of an accident previously evaluated. 2. Does the proposed amendment create the possibility of a new or different kind of accident from any accident previously evaluated? Response: No. PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 This request is for administrative changes only. No actual facility equipment or accident analyses will be affected by the proposed changes and no failure modes not bounded by previously evaluated accidents will be created. Therefore, this request will not create the possibility of a new or different kind of accident from any accident previously evaluated. 3. Does the proposed amendment involve a significant reduction in a margin of safety? Response: No. Margin of safety is associated with confidence in the ability of the fission product barriers (i.e., fuel cladding, reactor coolant system pressure boundary, and containment structure) to limit the level of radiation dose to the public. This request is for administrative changes only. No actual plant equipment or accident analyses will be affected by the proposed changes. Additionally, the proposed changes will not relax any criteria used to establish safety limits, will not relax any safety system settings, and will not relax the bases for any limiting conditions of operation. Therefore, these proposed changes will not involve a significant reduction in a margin of safety. The NRC staff has reviewed the licensee’s analysis and, based on this review, it appears that the three standards of 10 CFR 50.92(c) are satisfied. Therefore, the NRC staff proposes to determine that the amendment request involves no significant hazards consideration. The Commission is seeking public comments on this proposed determination. Any comments received within 30 days after the date of publication of this notice will be considered in making any final determination. Normally, the Commission will not issue the amendment until the expiration of 60 days after the date of publication of this notice. The Commission may issue the license amendment before expiration of the 60day period provided that its final determination is that the amendment involves no significant hazards consideration. In addition, the Commission may issue the amendment prior to the expiration of the 30-day comment period should circumstances change during the 30-day comment period such that failure to act in a timely way would result, for example, in derating or shutdown of the facility. Should the Commission take action prior to the expiration of either the comment period or the notice period, it will publish in the Federal Register a notice of issuance. Should the Commission make a final No Significant Hazards Consideration Determination, any hearing will take place after issuance. The Commission expects that the need to take this action will occur very infrequently. E:\FR\FM\03MRN1.SGM 03MRN1

Agencies

[Federal Register Volume 75, Number 41 (Wednesday, March 3, 2010)]
[Notices]
[Pages 9615-9616]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-4352]


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DEPARTMENT OF LABOR

Office of the Secretary


Bureau of International Labor Affairs: Labor Advisory Committee 
for Trade Negotiations and Trade Policy

ACTION: Meeting Notice.

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SUMMARY: Pursuant to the provisions of the Federal Advisory Committee 
Act (Pub. L. 92-463, as amended), notice is hereby given of a meeting 
of the Labor Advisory Committee for Trade Negotiation and Trade Policy.
    Date, Time, Place: March 16, 2010; 10:30 a.m.-11:30 a.m.; U.S. 
Department of Labor, Secretary's Conference Room, 200 Constitution 
Ave., NW., Washington, DC.
    Purpose: The meeting will include a review and discussion of 
current issues which influence U.S. trade policy. Potential U.S. 
negotiating objectives and bargaining positions in current and 
anticipated trade negotiations will be discussed. Pursuant to 19 U.S.C. 
2155(f) it has been determined that the meeting will be concerned with 
matters the disclosure of which would seriously compromise the 
Government's negotiating objectives or bargaining

[[Page 9616]]

positions. Accordingly, the meeting will be closed to the public.

FOR FURTHER INFORMATION CONTACT: Gregory Schoepfle, Director, Office of 
Trade and Labor Affairs; Phone: (202) 693-4887.

    Signed at Washington, DC, the 25th day of February 2010.
Sandra Polaski,
Deputy Undersecretary, International Affairs.
[FR Doc. 2010-4352 Filed 3-2-10; 8:45 am]
BILLING CODE 4510-28-P
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