Importer of Controlled Substances; Notice of Registration; Almac Clinical Services, Inc., 50162-50163 [2012-20370]
Download as PDF
50162
Federal Register / Vol. 77, No. 161 / Monday, August 20, 2012 / Notices
Additional written submissions to the
Commission, including requests
pursuant to section 201.12 of the
Commission’s rules, shall not be
accepted unless good cause is shown for
accepting such submissions, or unless
the submission is pursuant to a specific
request by a Commissioner or
Commission staff.
In accordance with sections 201.16(c)
and 207.3 of the Commission’s rules,
each document filed by a party to the
investigations must be served on all
other parties to the investigations (as
identified by either the public or BPI
service list), and a certificate of service
must be timely filed. The Secretary will
not accept a document for filing without
a certificate of service.
Authority: These investigations are being
conducted under authority of title VII of the
Tariff Act of 1930; this notice is published
pursuant to section 207.21 of the
Commission’s rules.
By order of the Commission.
Issued: August 15, 2012.
Lisa R. Barton,
Acting Secretary to the Commission.
[FR Doc. 2012–20372 Filed 8–17–12; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
1. On page 47109, in the third
column, the document heading should
appear as set forth above.
2. On page 47110, in the second
column, in the first full paragraph, in
the eighth line of text, ‘‘September 6,
2012’’ should read ‘‘September 19,
2012’’.
DEPARTMENT OF JUSTICE
[FR Doc. C1–2012–19197 Filed 8–17–12; 8:45 am]
In notice document 2012–19199
appearing on pages 47108–47109 in the
issue of Tuesday, August 7, 2012, make
the following corrections:
1. On page 47108, in the third
column, the document heading should
appear as set forth above.
2. On page 47109, in the sixth
paragraph following the table, in the
eighth line of text, ‘‘September 6, 2012’’
should read ‘‘September 19, 2012’’.
BILLING CODE 1505–01–D
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Application; Lipomed
Correction
[FR Doc. C1–2012–19196 Filed 8–17–12; 8:45 am]
Importer of Controlled Substances;
Notice of Application; SA INTL GMBH
C/O., Sigma Aldrich Co., LLC
BILLING CODE 1505–01–D
[FR Doc. C1–2012–19191 Filed 8–17–12; 8:45 am]
BILLING CODE 1505–01–D
DEPARTMENT OF JUSTICE
mstockstill on DSK4VPTVN1PROD with NOTICES
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Application; Clinical Supplies
Management, Inc.
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Application; R & D Systems,
Inc.
Correction
In notice document 2012–19193
appearing on pages 47110–47111 in the
issue of Tuesday, August 7, 2012, make
the following corrections:
1. On page 47110, in the third
column, the document heading should
appear as set forth above.
2. On page 47110, in the fifth
paragraph following the table, in the
eighth line of text, ‘‘September 6, 2012’’
should read ‘‘September 19, 2012’’.
[FR Doc. C1–2012–19193 Filed 8–17–12; 8:45 am]
BILLING CODE 1505–01–D
Correction
In notice document 2012–19197
appearing on pages 47109–47110 in the
issue of Tuesday, August 7, 2012, make
the following corrections:
VerDate Mar<15>2010
16:25 Aug 17, 2012
Jkt 226001
PO 00000
Frm 00085
Importer of Controlled Substances;
Notice of Application; Cerilliant
Corporation
Correction
[FR Doc. C1–2012–19199 Filed 8–17–12; 8:45 am]
In notice document 2012–19196
appearing on page 47108 in the issue of
Tuesday, August 7, 2012, make the
following corrections:
1. On page 47108, in the first column,
the document heading should appear as
set forth above.
2. On page 47108, in the second
column, in the second full paragraph, in
the eighth line of text, ‘‘September 6,
2012’’ should read ‘‘September 19,
2012’’.
Drug Enforcement Administration
Correction
In notice document 2012–19191
appearing on pages 47106–47108 in the
issue of Tuesday, August 7, 2012, make
the following corrections:
1. On page 47106, in the third
column, the document heading should
appear as set forth above.
2. On page 4707, in the sixth
paragraph following the table, in the
eighth line of text, ‘‘September 6, 2012’’
should read ‘‘September 19, 2012’’.
Drug Enforcement Administration
Fmt 4703
Sfmt 4703
BILLING CODE 1505–01–D
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Registration; Almac Clinical
Services, Inc.
By Notice dated April 17, 2012, and
published in the Federal Register on
April 26, 2012, 77 FR 24985, Almac
Clinical Services, Inc., (ACSI), 25 Fretz
Road, Souderton, Pennsylvania 18964,
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
Oxycodone (9143) ........................
Hydromorphone (9150) ................
Tapentadol (9780) ........................
Fentanyl (9801) ............................
Schedule
II
II
II
II
The company plans to import small
quantities of the listed controlled
substances in dosage form to conduct
clinical trials.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and 952(a),
and determined that the registration of
Almac Clinical Services, Inc. (ACSI) 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
Almac Clinical Services, Inc. (ACSI) to
ensure that the company’s registration is
consistent with the public interest.
The investigation has included
inspection and testing of the company’s
E:\FR\FM\20AUN1.SGM
20AUN1
Federal Register / Vol. 77, No. 161 / Monday, August 20, 2012 / Notices
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 the basic classes of
controlled substances listed.
Dated: August 7, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2012–20370 Filed 8–17–12; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Registration; Research
Triangle Institute
Correction
In notice document 2012–19208
appearing on pages 47111–47114 in the
issue of Tuesday, August 7, 2012, make
the following correction:
On page 47111, in the second column,
the document heading should appear as
set forth above.
[FR Doc. C1–2012–19208 Filed 8–17–12; 8:45 am]
BILLING CODE 1505–01–D
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Drug
Schedule
4-Anilino-N-phenethyl-4-piperidine
(8333).
Thebaine (9333) ...........................
II
II
The company plans on manufacturing
the listed controlled substances as bulk
intermediates for distribution 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 Cody Laboratories, Inc. to
manufacture the listed basic classes of
controlled substances is consistent with
the public interest at this time. DEA has
investigated Cody Laboratories, 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: August 7, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
Importer of Controlled Substances;
Notice of Registration; Catalent
Pharma Solutions, Inc.
Correction
In notice document 2012–19202
appearing on page 47114 in the issue of
Tuesday, August 7, 2012, make the
following correction:
On page 47114, in the first column,
the document heading should appear as
set forth above.
[FR Doc. C1–2012–19202 Filed 8–17–12; 8:45 am]
BILLING CODE 1505–01–D
Laboratories, Inc., 601 Yellowstone
Avenue, Cody, Wyoming 82414, made
application by letter to the Drug
Enforcement Administration (DEA) to
be registered as a bulk manufacturer of
the following basic classes of controlled
substances:
[FR Doc. 2012–20369 Filed 8–17–12; 8:45 am]
BILLING CODE 4410–09–P
mstockstill on DSK4VPTVN1PROD with NOTICES
Drug Enforcement Administration
Manufacturer of Controlled
Substances, Notice of Registration,
Cody Laboratories, Inc.
Mine Safety and Health Administration
Affirmative Decisions on Petitions for
Modification Granted in Whole or in
Part
Mine Safety and Health
Administration (MSHA), Labor.
ACTION: Notice.
By Notice dated March 8, 2012, and
published in the Federal Register on
March 20, 2012, 77 FR 16263, Cody
VerDate Mar<15>2010
16:25 Aug 17, 2012
Jkt 226001
Section 101(c) of the Federal
Mine Safety and Health Act of 1977 and
30 CFR part 44 govern the application,
processing, and disposition of petitions
for modification. This Federal Register
Notice notifies the public that MSHA
has investigated and issued a final
SUMMARY:
PO 00000
Frm 00086
Fmt 4703
Sfmt 4703
decision on certain mine operator
petitions to modify a safety standard.
ADDRESSES: Copies of the final decisions
are posted on MSHA’s Web Site at
https://www.msha.gov/indexes/
petition.htm. The public may inspect
the petitions and final decisions during
normal business hours in MSHA’s
Office of Standards, Regulations and
Variances, 1100 Wilson Boulevard,
Room 2349, Arlington, Virginia 22209.
All visitors must first stop at the
receptionist desk on the 21st Floor to
sign-in.
FOR FURTHER INFORMATION CONTACT:
Roslyn B. Fontaine, Office of Standards,
Regulations and Variances at 202–693–
9475 (Voice), fontaine.roslyn@dol.gov
(Email), or 202–693–9441 (Telefax), or
Barbara Barron at 202–693–9447
(Voice), barron.barbara@dol.gov
(Email), or 202–693–9441 (Telefax).
[These are not toll-free numbers].
SUPPLEMENTARY INFORMATION:
I. Introduction
Under section 101 of the Federal Mine
Safety and Health Act of 1977, a mine
operator may petition and the Secretary
of Labor (Secretary) may modify the
application of a mandatory safety
standard to that mine if the Secretary
determines that: (1) an alternative
method exists that will guarantee no
less protection for the miners affected
than that provided by the standard; or
(2) that the application of the standard
will result in a diminution of safety to
the affected miners.
MSHA bases the final decision on the
petitioner’s statements, any comments
and information submitted by interested
persons, and a field investigation of the
conditions at the mine. In some
instances, MSHA may approve a
petition for modification on the
condition that the mine operator
complies with other requirements noted
in the decision.
II. Granted Petitions for Modification
DEPARTMENT OF LABOR
AGENCY:
DEPARTMENT OF JUSTICE
50163
On the basis of the findings of
MSHA’s investigation, and as designee
of the Secretary, MSHA has granted or
partially granted the following petitions
for modification:
• Docket Number: M–2009–050–C.
FR Notice: 75 FR 3256 (1/20/2010).
Petitioner: Wolf Run Mining
Company, 300 Corporate Centre Drive,
Scott Depot, West Virginia 25560.
Mine: Sentinel Mine, MSHA I.D. No.
46–04168, located in Barbour County,
West Virginia.
Regulation Affected: 30 CFR 75.1700
(Oil and gas wells).
• Docket Number: M–2009–052–C.
FR Notice: 75 FR 3257 (1/20/2010).
E:\FR\FM\20AUN1.SGM
20AUN1
Agencies
[Federal Register Volume 77, Number 161 (Monday, August 20, 2012)]
[Notices]
[Pages 50162-50163]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-20370]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances; Notice of Registration; Almac
Clinical Services, Inc.
By Notice dated April 17, 2012, and published in the Federal
Register on April 26, 2012, 77 FR 24985, Almac Clinical Services, Inc.,
(ACSI), 25 Fretz Road, Souderton, Pennsylvania 18964, 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
------------------------------------------------------------------------
Oxycodone (9143)........................... II
Hydromorphone (9150)....................... II
Tapentadol (9780).......................... II
Fentanyl (9801)............................ II
------------------------------------------------------------------------
The company plans to import small quantities of the listed
controlled substances in dosage form to conduct clinical trials.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a) and 952(a), and determined that the
registration of Almac Clinical Services, Inc. (ACSI) 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 Almac Clinical Services, Inc. (ACSI) to ensure that the
company's registration is consistent with the public interest.
The investigation has included inspection and testing of the
company's
[[Page 50163]]
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 the basic classes of controlled
substances listed.
Dated: August 7, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-20370 Filed 8-17-12; 8:45 am]
BILLING CODE 4410-09-P