Importer of Controlled Substances; Notice of Registration, 65749-65750 [2011-27430]
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Federal Register / Vol. 76, No. 205 / Monday, October 24, 2011 / Notices
JUDICIAL CONFERENCE OF THE
UNITED STATES
Hearing of the Judicial Conference
Committee on Civil Rules
Judicial Conference of the
United States, Advisory Committee on
Civil Rules.
ACTION: Notice of cancellation of open
hearing.
AGENCY:
The following public hearing
on proposed amendments to the Federal
Rules of Civil Procedure has been
canceled: Civil Rules Hearing,
November 7, 2011, in Washington, DC.
FOR FURTHER INFORMATION CONTACT:
Benjamin J. Robinson, Deputy Rules
Officer and Counsel, Rules Committee
Support Office, Administrative Office of
the United States Courts, Washington,
DC 20544, telephone (202) 502–1820.
SUMMARY:
BILLING CODE 2210–55–P
DEPARTMENT OF JUSTICE
Antitrust Division
tkelley on DSK3SPTVN1PROD with NOTICES
Notice Pursuant to the National
Cooperative Research and Production
Act of 1993—DVD Copy Control
Association
Notice is hereby given that, on August
26, 2011, pursuant to Section 6(a) of the
National Cooperative Research and
Production Act of 1993, 15 U.S.C. 4301
et seq. (‘‘the Act’’), DVD Copy Control
Association (‘‘DVD CCA’’) has filed
written notifications simultaneously
with the Attorney General and the
Federal Trade Commission disclosing
changes in its membership. The
notifications were filed for the purpose
of extending the Act’s provisions
limiting the recovery of antitrust
plaintiffs to actual damages under
specified circumstances. Specifically,
NEC USA, Inc., New York, NY;
Chicovery Co., Ltd., San Chung City,
Taipei, Taiwan; Meiloon Industrial Co.,
Ltd., Taoyuan City, Taiwan; MIT
Technology Co., Ltd., Dongguan,
Guangdong, People’s Republic of China;
and IMS International Media Service
S.p.A., Varese, Italy, have withdrawn as
parties to this venture.
No other changes have been made in
either the membership or planned
activity of the group research project.
Membership in this group research
project remains open, and DVD CCA
intends to file additional written
Jkt 226001
[FR Doc. 2011–27215 Filed 10–21–11; 8:45 am]
BILLING CODE M
DEPARTMENT OF JUSTICE
Notice Pursuant to the National
Cooperative Research and Production
Act of 1993—TAI and Southwest
Research Institute
[FR Doc. 2011–27419 Filed 10–21–11; 8:45 am]
15:34 Oct 21, 2011
Patricia A. Brink,
Director of Civil Enforcement, Antitrust
Division.
Antitrust Division
Dated: October 18, 2011.
Benjamin J. Robinson,
Deputy Rules Officer and Counsel.
VerDate Mar<15>2010
notifications disclosing all changes in
membership.
On April 11, 2001, DVD CCA filed its
original notification pursuant to Section
6(a) of the Act. The Department of
Justice published a notice in the Federal
Register pursuant to Section 6(b) of the
Act on August 3, 2001 (66 FR 40727).
The last notification was filed with
the Department on June 23, 2011. A
notice was published in the Federal
Register pursuant to Section 6(b) of the
Act on July 20, 2011 (76 FR 43348).
Notice is hereby given that, on August
24, 2011, pursuant to Section 6(a) of the
National Cooperative Research and
Production Act of 1993, 15 U.S.C. 4301
et seq. (‘‘the Act’’), TAI and SwRI
Consortium for Advanced Research for
the Development of Telecommunication
and Security Tools (‘‘TAISR’’) has filed
written notifications simultaneously
with the Attorney General and the
Federal Trade Commission disclosing
(1) the identities of the parties to the
venture and (2) the nature and objective
of the venture. The notifications were
filed for the purpose of extending the
Act’s provisions limiting the recovery of
antitrust plaintiffs to actual damages
under specified circumstances. Pursuant
to Section 6(b) of the Act, the identities
of the parties to the venture are:
Southwest Research Institute, San
Antonio, TX, and Tridex Associates,
Inc., Woodbridge, VA.
The general area of TAISR’s planned
activities is to advance the field of
security and telecommunications tools
research and development by organizing
and implementing joint engineering and
scientific research activities. These
activities will encompass the
development of sophisticated
telecommunication tools and or
components in the engineering and
scientific areas of electronic systems,
hardware design, packaging and rapid
prototyping.
Membership in this research group is
closed, and the participants intend to
file additional written notification
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
disclosing all changes in planned
activities.
Patricia A. Brink,
Director of Civil Enforcement, Antitrust
Division.
[FR Doc. 2011–27114 Filed 10–21–11; 8:45 am]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Registration
By Notice dated August 9, 2011, and
published in the Federal Register on
August 18, 2011, 76 FR 51399, Aptuit,
10245 Hickman Mills Drive, Kansas
City, Missouri 64137, made application
by renewal to the Drug Enforcement
Administration (DEA) to be registered as
an importer of the following basic
classes of controlled substances:
Drug
Marihuana (7360) .........................
Poppy Straw Concentrate (9670)
Schedule
I
II
The company plans to import a
finished pharmaceutical product
containing cannabis extracts in dosage
form for packaging for a clinical trial
study. In addition, the company also
plans to import an ointment for the
treatment of wounds which contains
trace amounts of the controlled
substances normally found in poppy
straw concentrate for packaging and
labeling for clinical trials.
Comments and requests for hearings
on applications to import narcotic raw
material are not appropriate. 72 FR 3417
(2007).
DEA has considered the factors in 21
U.S.C. 823(a) and 952(a), and
determined that the registration of
Aptuit to import the basic classes of
controlled substances is consistent with
the public interest and with United
States obligations under international
treaties, conventions, or protocols in
effect on May 1, 1971. DEA has
investigated Aptuit 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. 952(a)
and 958(a), and in accordance with 21
CFR 1301.34, the above named company
is granted registration as an importer of
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65750
Federal Register / Vol. 76, No. 205 / Monday, October 24, 2011 / Notices
the basic classes of controlled
substances listed.
Dated: October 3, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2011–27430 Filed 10–21–11; 8:45 am]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Registration
By Notice dated June 7, 2011, and
published in the Federal Register on
June 16, 2011, 76 FR 35243, American
Radiolabeled Chemicals, 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 following basic classes of controlled
substances:
Drug
tkelley on DSK3SPTVN1PROD with NOTICES
Dated: October 3, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
(Pub. L. 94–409) (5 U.S.C. 552b)
[FR Doc. 2011–27424 Filed 10–21–11; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
I
Advisory Board Meeting
Time and Date: 8 a.m. to 4:30 p.m. on
Wednesday, November 2, 2011, 8 a.m.
to 4:30 p.m. on Thursday, November 3,
2011.
Place: Stanford University Law
School, 550 Nathan Abbott Way,
Stanford, California, (650) 724–6258.
Matters To Be Considered:
Organizational culture and change in
the correctional environment;
Performance Based Outcomes; Director’s
report; Presentations.
Contact Person for More Information:
Thomas Beauclair, Deputy Director,
202–307–3106, ext. 44254.
I
I
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
Morris L. Thigpen,
Director.
[FR Doc. 2011–27157 Filed 10–21–11; 8:45 am]
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II
II
II
II
II
II
Jkt 226001
DEPARTMENT OF JUSTICE
United States Parole Commission
Sunshine Act Meeting; Record of Vote
of Meeting Closure
I, Isaac Fulwood, of the United States
Parole Commission, was present at a
meeting of said Commission, which
started at approximately 11 a.m., on
Thursday, September 8, 2011, at the
U.S. Parole Commission, 90 K Street,
PO 00000
Frm 00070
Fmt 4703
Sfmt 4703
In witness whereof, I make this official
record of the vote taken to close this
meeting and authorize this record to be
made available to the public.
Dated: September 15, 2011.
Isaac Fulwood,
Chairman, U.S. Parole Commission.
[FR Doc. 2011–27571 Filed 10–20–11; 4:15 pm]
National Institute of Corrections
I
I
I
I
I
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
15:34 Oct 21, 2011
NE., Third Floor, Washington, DC
20530. The purpose of the meeting was
to discuss four original jurisdiction
cases pursuant to 28 CFR 2.27. Four
Commissioners were present,
constituting a quorum when the vote to
close the meeting was submitted.
Public announcement further
describing the subject matter of the
meeting and certifications of the General
Counsel that this meeting may be closed
by votes of the Commissioners present
were submitted to the Commissioners
prior to the conduct of any other
business. Upon motion duly made,
seconded, and carried, the following
Commissioners voted that the meeting
be closed: Isaac Fulwood, Cranston J.
Mitchell, Patricia Cushwa and J. Patricia
Wilson Smoot.
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) .....................
Heroin (9200) ...............................
Meperidine (9230) ........................
Metazocine (9240) ........................
Dextropropoxyphene, bulk (nondosage forms) (9273).
Morphine (9300) ...........................
Oripavine (9330) ...........................
Thebaine (9333) ...........................
Oxymorphone (9652) ...................
Phenazocine (9715) .....................
Fentanyl (9801) ............................
VerDate Mar<15>2010
American Radiolabeled Chemicals, Inc.
to manufacture the listed basic classes
of controlled substances is consistent
with the public interest at this time.
DEA has investigated American
Radiolabeled Chemicals 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 classes of controlled
substances listed.
BILLING CODE 4410–01–P
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[Notice (11–105)]
Aerospace Safety Advisory Panel;
Charter Renewal
National Aeronautics and
Space Administration (NASA).
ACTION: Notice of renewal and
amendment of the charter of the NASA
Aerospace Safety Advisory Panel.
AGENCY:
Pursuant to sections 14(b)(1)
and 9(c) of the Federal Advisory
Committee Act (Pub. L. 92–463), and
after consultation with the Committee
Management Secretariat, General
Services Administration, the NASA
Administrator has determined that a
renewal and amendment of the charter
of the NASA Aerospace Safety Advisory
Panel is in the public interest in
connection with the performance of
duties imposed on NASA by law. The
renewed charter is for a two-year period
ending October 13, 2013. It is identical
to the previous charter in all respects
except it removes references to areas of
responsibility that are no longer
applicable, updates legal citations, and
conforms the text to the most recent
Congressional reauthorization for this
Federal advisory committee (Pub. L.
111–314 on December 18, 2010).
SUMMARY:
E:\FR\FM\24OCN1.SGM
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]]>Agencies
[Federal Register Volume 76, Number 205 (Monday, October 24, 2011)]
[Notices]
[Pages 65749-65750]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-27430]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances; Notice of Registration
By Notice dated August 9, 2011, and published in the Federal
Register on August 18, 2011, 76 FR 51399, Aptuit, 10245 Hickman Mills
Drive, Kansas City, Missouri 64137, made application by renewal to the
Drug Enforcement Administration (DEA) to be registered as an importer
of the following basic classes of controlled substances:
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Marihuana (7360)........................... I
Poppy Straw Concentrate (9670)............. II
------------------------------------------------------------------------
The company plans to import a finished pharmaceutical product
containing cannabis extracts in dosage form for packaging for a
clinical trial study. In addition, the company also plans to import an
ointment for the treatment of wounds which contains trace amounts of
the controlled substances normally found in poppy straw concentrate for
packaging and labeling for clinical trials.
Comments and requests for hearings on applications to import
narcotic raw material are not appropriate. 72 FR 3417 (2007).
DEA has considered the factors in 21 U.S.C. 823(a) and 952(a), and
determined that the registration of Aptuit to import the basic classes
of controlled substances is consistent with the public interest and
with United States obligations under international treaties,
conventions, or protocols in effect on May 1, 1971. DEA has
investigated Aptuit 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. 952(a) and 958(a), and in accordance with 21 CFR 1301.34,
the above named company is granted registration as an importer of
[[Page 65750]]
the basic classes of controlled substances listed.
Dated: October 3, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2011-27430 Filed 10-21-11; 8:45 am]
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