Notice of Sunshine Act Meeting, 5849-5850 [2012-2635]

Download as PDF Federal Register / Vol. 77, No. 24 / Monday, February 6, 2012 / Notices Dated: January 27, 2012. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration [FR Doc. 2012–2591 Filed 2–3–12; 8:45 am] By Notice dated September 28, 2011, and published in the Federal Register on October 7, 2011, 76 FR 62449, Cambrex Charles City, Inc., 1205 11th Street, Charles City, Iowa 50616, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the following basic classes of controlled substances: Drug Schedule mstockstill on DSK4VPTVN1PROD with NOTICES Gamma Hydroxybutyric Acid (GHB) (2010). Amphetamine (1100) .................... Lisdexamfetamine (1205) ............. Methylphenidate (1724) ................ 4-Anilino-N-phenethyl-4-piperidine (8333). Phenylacetone (8501) .................. Codeine (9050) ............................. Oxycodone (9143) ........................ Hydromorphone (9150) ................ Dextropropoxyphene, bulk (nondosage forms) (9273). Morphine (9300) ........................... Oripavine (9330) ........................... Thebaine (9333) ........................... Opium raw (9600) ........................ Oxymorphone (9652) ................... Poppy Straw Concentrate (9670) Sufentanil (9740) .......................... Fentanyl (9801) ............................ I II II II II II II II II II II II II II II II II II The company will 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 Cambrex Charles City, Inc. to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Cambrex Charles City, 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 USC § 823(a), 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. VerDate Mar<15>2010 17:27 Feb 03, 2012 Jkt 226001 BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated September 28, 2011, and published in the Federal Register on October 7, 2011, 76 FR 62450, GE Healthcare, 3350 North Ridge Avenue, Arlington Heights, Illinois 60004–1412, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Cocaine (9041), a basic class of controlled substance listed in schedule II. The company plans to manufacture a radioactive product to diagnose Parkinson’s disease, and to manufacture a bulk investigational new drug (IND) for clinical trials. 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 GE Healthcare to manufacture the listed basic class of controlled substance is consistent with the public interest at this time. DEA has investigated GE Healthcare 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(a), and in accordance with 21 CFR 1301.33, the above named company is granted registration as a bulk manufacturer of the basic class of controlled substance listed. Dated: January 26, 2012. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2012–2586 Filed 2–3–12; 8:45 am] BILLING CODE 4410–09–P PO 00000 5849 DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated June 23, 2011, and published in the Federal Register on July 5, 2011, 76 FR 39127, Johnson Matthey Pharmaceutical Materials, Inc., Pharmaceuticals Service, 25 Patton Road, Devens, Massachusetts 01434, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Remifentanil (9739), the basic class of controlled substance in schedule II. The company plans to utilize this facility to manufacture small quantities of the listed controlled substance in bulk and to conduct analytical testing in support of the company’s primary manufacturing facility in West Deptford, New Jersey. The controlled substances manufactured in bulk at this facility will be distributed to the company’s 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 Pharmaceutical Materials, Inc. to manufacture the listed basic class of controlled substance is consistent with the public interest at this time. DEA has investigated Johnson Matthey Pharmaceutical Materials, 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(a), and in accordance with 21 CFR 1301.33, the above named company is granted registration as a bulk manufacturer of the basic class of controlled substance listed. Dated: January 27, 2012. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2012–2568 Filed 2–3–12; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Parole Commission Notice of Sunshine Act Meeting 11:30 a.m., Thursday, February 9, 2012. TIME AND DATE: Frm 00095 Fmt 4703 Sfmt 4703 E:\FR\FM\06FEN1.SGM 06FEN1 5850 Federal Register / Vol. 77, No. 24 / Monday, February 6, 2012 / Notices U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, DC. STATUS: Closed. MATTERS TO BE CONSIDERED: Determination on one original jurisdiction case. PLACE: CONTACT PERSON FOR MORE INFORMATION: Patricia W. Moore, Staff Assistant to the Chairman, U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, DC 20530, (202) 346–7001. Dated: January 31, 2012. Rockne Chickinell, General Counsel, U.S. Parole Commission. [FR Doc. 2012–2635 Filed 2–2–12; 4:15 pm] BILLING CODE 4410–31–P DEPARTMENT OF JUSTICE Parole Commission Notice of Sunshine Act Meeting 10 a.m., Thursday, February 9, 2012. PLACE: U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, DC. STATUS: Open. MATTERS TO BE CONSIDERED: Approval of December 8, 2011 minutes; reports from the Chairman, the Commissioners, and senior staff; Mental Health Docket. CONTACT PERSON FOR MORE INFORMATION: Patricia W. Moore, Staff Assistant to the Chairman, U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, DC 20530, (202) 346–7001. TIME AND DATE: Dated: January 31, 2012. Rockne Chickinell, General Counsel, U.S. Parole Commission. [FR Doc. 2012–2637 Filed 2–2–12; 4:15 pm] BILLING CODE 4410–31–P DEPARTMENT OF LABOR Employment and Training Administration Notice of Random Assignment Study To Evaluate Workforce Investment Act Adult and Dislocated Worker Programs; Final Notice Employment and Training Administration (ETA), Labor. ACTION: Notice. mstockstill on DSK4VPTVN1PROD with NOTICES AGENCY: The Employment and Training Administration (ETA) of the Department of Labor (DOL or the Department) will conduct an evaluation to provide rigorous, nationallyrepresentative estimates of the net impacts of intensive services and training provided under the Workforce SUMMARY: VerDate Mar<15>2010 17:27 Feb 03, 2012 Jkt 226001 Investment Act (WIA) Adult and Dislocated Worker Programs. The Department has determined that it is in the public interest to use a random assignment impact methodology for the study. This methodology will provide ETA with estimates of the net impacts of WIA intensive services and training that are offered during the evaluation study period. On July 21, 2011 (76 FR 43729–43731), the Department solicited comments concerning the Department’s plan to use random assignment methodology in carrying out the study. This notice is to provide the Department’s response to the comments received. FOR FURTHER INFORMATION CONTACT: Eileen Pederson, U.S. Department of Labor, Employment and Training Administration, Office of Policy Development and Research, 200 Constitution Avenue NW., Frances Perkins Bldg., Room N–5641, Washington, DC, 20210. Telephone: (202) 693–3647 (this is not a toll-free number) or email: pederson.eileen@dol.gov. Individuals with hearing or speech impairments may access the telephone number above via TTY by calling the toll-free Federal Information Relay Service at 1–(877) 889–5627 (TTY/TDD). SUPPLEMENTARY INFORMATION: I. Background On July 21, 2011, the Department announced its plans to conduct an evaluation of the net impacts of intensive services and training provided under WIA (Pub. L. 105–220) Adult and Dislocated Worker Programs. To obtain rigorous, nationally representative estimates of WIA’s effectiveness for adults and dislocated workers, the Department determined that it would use random assignment impact methodology for the evaluation. The design of the study was described as follows: The evaluation will be done in approximately 30 randomly selected LWIAs. WIA applicants in the selected LWIAs who are eligible for intensive services would be randomly assigned to one of three groups. The three research groups to which they would be assigned are: (1) The full-WIA group—adults and dislocated workers in this group can receive any WIA services and training for which they are eligible, (2) the coreand-intensive group—adults and dislocated workers in this group can receive any WIA services for which they are eligible but no training, and (3) the core-only group—adults and dislocated workers in this group can receive only WIA core services but no intensive services or training. PO 00000 Frm 00096 Fmt 4703 Sfmt 4703 In the LWIAs selected for the study, all applicants for intensive services and/ or training will be asked to participate in the study during the 12–18 month study enrollment period. They will be informed of the evaluation, provided an opportunity to ask questions or seek clarification of their role and responsibilities should they agree to participate, and then required to give their consent to participate. Applicants who do not consent to participate in the study will not be randomly assigned to one of the study groups but will be allowed to receive core services only. The participant enrollment period will range between 12 and 18 months in each LWIA. To protect the rights and welfare of WIA program applicants who agree to participate in the evaluation, the evaluation team, led by researchers from Mathematica and its subcontractor MDRC, submitted the WIA Adult and Dislocated Worker Programs evaluation design to MDRC’s Institutional Review Board (IRB) for concurrence. An IRB is a committee specifically responsible for protecting the rights and welfare of humans involved in biomedical and behavioral research. On June 17, 2010, MDRC’s IRB determined this study to be of no more than minimal risk and approved it. The Department requested comments concerning its intent to carry out the random assignment study described above. The Department asked for comments focused on whether there is a methodology that would yield as credible and reliable impacts of the WIA programs as random assignment, but avoids adverse effect on the study participants. The Department also welcomed comments that suggest ways to more effectively minimize any adverse impact on the study participants who participate in the study described above. II. Discussion of Comments Received The Department received comments from four sources in response to the notice. The comments were received from two workforce departments, one advocacy group, and one private citizen. The Department’s responses to the comments are provided below. Comment: Two commenters asked about how other sources of funding for services would be accounted for in the study. One of these commenters asked whether the core-only group would have access to other partner services and, if so, the commenter suggested that the study take it into account through the follow-up survey. The other commenter was concerned that the study would not capture the nature of E:\FR\FM\06FEN1.SGM 06FEN1

Agencies

[Federal Register Volume 77, Number 24 (Monday, February 6, 2012)]
[Notices]
[Pages 5849-5850]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-2635]


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DEPARTMENT OF JUSTICE

Parole Commission


Notice of Sunshine Act Meeting

TIME AND DATE: 11:30 a.m., Thursday, February 9, 2012.

[[Page 5850]]


PLACE: U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, 
DC.

STATUS: Closed.

MATTERS TO BE CONSIDERED: Determination on one original jurisdiction 
case.

CONTACT PERSON FOR MORE INFORMATION: Patricia W. Moore, Staff Assistant 
to the Chairman, U.S. Parole Commission, 90 K Street NE., 3rd Floor, 
Washington, DC 20530, (202) 346-7001.

    Dated: January 31, 2012.
Rockne Chickinell,
General Counsel, U.S. Parole Commission.
[FR Doc. 2012-2635 Filed 2-2-12; 4:15 pm]
BILLING CODE 4410-31-P

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