Agency Information Collection Activities; Proposed eCollection eComments Requested; Extension of a Previously Approved Collection; Application for Permit To Import Controlled Substances for Domestic and/or Scientific Purposes, 62397-62398 [2023-19536]
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62397
Federal Register / Vol. 88, No. 174 / Monday, September 11, 2023 / Notices
import, and export regulated
transactions in listed chemicals are
submitted electronically through the
Diversion Control Division secure
network application. Any person who
desires to import non-narcotic
substances in schedules III, IV, and V
must electronically file their return
information. Any person who desires to
export non-narcotic substances in
schedules III and IV and any other
substance in schedule V is also required
to electronically file a controlled
substances import declaration/
controlled substance export invoice.
Overview of This Information
Collection
1. Type of Information Collection:
Extension of a previously approved
collection.
2. The Title of the Form/Collection:
Import/Export Declaration for List I and
List II Chemicals.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
DEA Forms: 486, 486A. The applicable
component within the Department of
Justice is the Drug Enforcement
Administration, Office of Diversion
Control.
4. Affected public who will be asked
or required to respond, as well as the
obligation to respond: Affected Public
(Primary): Private Sector—businesses or
other for-profit institutions, and not-forprofit institutions. Other: State, local
and tribal governments, Federal
Government. The obligation to respond
is mandatory per 21 CFR part 1313.
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: The DEA estimates that 631
registrants participate in this
information collection. The time per
response is 11 minutes to complete the
DEA–486 Import, DEA–486
International, and DEA–486A Import.
The time per response is 12 minutes to
complete DEA–486 Export.
6. An estimate of the total annual
burden (in hours) associated with the
collection: DEA estimates that this
collection takes 4,134 annual burden
hours.
7. An estimate of the total annual cost
burden associated with the collection, if
applicable: $0.
TOTAL BURDEN HOURS
Number of
respondents
Activity
Total annual
responses
Time per
response
(minutes)
Total annual
burden
(hours)
DEA–486 Import ..................................................................
DEA–486 Export ..................................................................
DEA–486 International .........................................................
DEA–486A Import ................................................................
164
204
99
164
16
77
4
16
2,686
15,737
429
2,686
11
12
11
11
457
3,147
73
457
Unduplicated Totals ......................................................
631
34
21,538
........................
4,134
If additional information is required
contact: Darwin Arceo, Department
Clearance Officer, United States
Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street NE, 4W–218,
Washington, DC.
Dated: September 5, 2023.
Darwin Arceo,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2023–19539 Filed 9–8–23; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
[OMB Number 1117–0013]
ddrumheller on DSK120RN23PROD with NOTICES1
Frequency
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Extension of a
Previously Approved Collection;
Application for Permit To Import
Controlled Substances for Domestic
and/or Scientific Purposes
Drug Enforcement
Administration, Department of Justice.
ACTION: 60-Day notice.
AGENCY:
The Drug Enforcement
Administration (DEA), Department of
Justice (DOJ), will be submitting the
SUMMARY:
VerDate Sep<11>2014
18:16 Sep 08, 2023
Jkt 259001
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995.
DATES: Comments are encouraged and
will be accepted for 60 days until
November 13, 2023.
FOR FURTHER INFORMATION CONTACT: If
you have additional comments
especially on the estimated public
burden or associated response time,
suggestions, or need a copy of the
proposed information collection
instrument with instructions or
additional information, please contact
Scott A. Brinks, Regulatory Drafting and
Policy Support Section, Drug
Enforcement Administration; Mailing
Address: 8701 Morrissette Drive,
Springfield, Virginia 22152; Telephone:
(571) 362–3261, Email: scott.a.brinks@
dea.gov.
Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00083
Fmt 4703
Sfmt 4703
functions of the Bureau of Justice
Statistics, including whether the
information will have practical utility;
—Evaluate the accuracy of the agency’s
estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
—Evaluate whether and if so how the
quality, utility, and clarity of the
information to be collected can be
enhanced; and
—Minimize the burden of the collection
of information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
Abstract: Section 1002 of the
Controlled Substances Import and
Export Act (CSIEA) (21 U.S.C. 952) and
Title 21, Code of Federal Regulations 21
CFR, sections 1312.11, 1312.12 and
1312.13 requires any person who
desires to import controlled substances
listed in schedules I or II, any narcotic
substance listed in schedules III or IV,
or any non-narcotic substance in
schedule III which the Administrator
has specifically designated by regulation
in section 1312.30, or any nonnarcotic
E:\FR\FM\11SEN1.SGM
11SEN1
62398
Federal Register / Vol. 88, No. 174 / Monday, September 11, 2023 / Notices
substance in schedule IV or V which is
also listed in schedule I or II of the
Convention on Psychotropic
Substances, must have an import
permit. To obtain the permit to import
controlled substances for domestic and
or scientific purposes, an application for
the permit must be made to the DEA, on
DEA Form 357.
Overview of This Information
Collection
1. Type of Information Collection:
Extension of a previously approved
collection.
2. The Title of the Form/Collection:
Application for Permit to Import
Controlled Substances for Domestic
and/or Scientific Purposes.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
DEA Form 357. The applicable
component within the Department of
Justice is the Drug Enforcement
Administration, Office of Diversion
Control.
4. Affected public who will be asked
or required to respond, as well as the
obligation to respond: Affected Public:
Private Sector—businesses or other forprofit institutions. The obligation to
respond is mandatory per 21 CFR,
sections 1312.11, 1312.12 and 1312.13.
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: The DEA estimates that 124
registrants participate in this
information collection. The time per
response is 21 minutes to complete the
DEA–357 (paper) and 15 minutes to
complete DEA–357 (online).
6. An estimate of the total annual
burden (in hours) associated with the
collection: DEA estimates that this
collection takes 264.35 annual burden
hours.
7. An estimate of the total annual cost
burden associated with the collection, if
applicable: $0.
TOTAL BURDEN HOURS
Number of
respondents
Activity
Time per
response
(min.)
Total annual
burden
(hours)
DEA Form: 357 (online) .......................................................
DEA Form: 357 (paper) .......................................................
124
9
958
71
15
21
266
19
Unduplicated Totals ......................................................
124
........................
1,081
0.26
264.35
If additional information is required
contact: Darwin Arceo, Department
Clearance Officer, United States
Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street NE, 4W–218,
Washington, DC.
Dated: September 5, 2023.
Darwin Arceo,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2023–19536 Filed 9–8–23; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
[OMB Number 1117–0024]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Revision of a
Previously Approved Collection;
Report of Loss or Disappearance of
Listed Chemicals and Regulated
Transactions in Tableting/
Encapsulating Machines
Drug Enforcement
Administration, Department of Justice.
ACTION: 60-Day notice.
AGENCY:
ddrumheller on DSK120RN23PROD with NOTICES1
Total annual
responses
Frequency
The Drug Enforcement
Administration (DEA), Department of
Justice (DOJ), will be submitting the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
SUMMARY:
VerDate Sep<11>2014
17:10 Sep 08, 2023
Jkt 259001
accordance with the Paperwork
Reduction Act of 1995.
DATES: Comments are encouraged and
will be accepted for 60 days until
November 13, 2023.
FOR FURTHER INFORMATION CONTACT: If
you have additional comments
especially on the estimated public
burden or associated response time,
suggestions, or need a copy of the
proposed information collection
instrument with instructions or
additional information, please contact
Scott A Brinks, Regulatory Drafting and
Policy Support Section, Drug
Enforcement Administration; Mailing
Address: 8701 Morrissette Drive,
Springfield, Virginia 22152; Telephone:
(571) 362–3261, Email: scott.a.brinks@
dea.gov.
Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the Bureau of Justice
Statistics, including whether the
information will have practical utility;
—Evaluate the accuracy of the agency’s
estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00084
Fmt 4703
Sfmt 4703
—Evaluate whether and if so how the
quality, utility, and clarity of the
information to be collected can be
enhanced; and
—Minimize the burden of the collection
of information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
Abstract: Each regulated person is
required to report any unusual or
excessive loss or disappearance of a
listed chemical, and any regulated
transaction in a tableting or
encapsulating machine, to include any
domestic regulated transaction in a
tableting or encapsulating machine and
any import or export of a tableting or
encapsulating machine. 21 U.S.C. 830
(b)(1)(A), (C) and (D); 21 CFR
1310.05(a)(1), (3)–(4); 21 CFR
1310.05(c). Regulated persons include
manufacturers, distributors, importers,
and exporters of listed chemicals,
tableting machines, or encapsulating
machines, or persons who serve as
brokers or traders for international
transactions involving a listed chemical,
tableting machine, or encapsulating
machine. 21 CFR 1300.02(b). This report
will be submitted electronically. DEA
will be modifying this collection (1117–
0024) and collection 1117–0001 by
removing Form 107 from this collection
and adding it to 1117–0001 because
E:\FR\FM\11SEN1.SGM
11SEN1
Agencies
[Federal Register Volume 88, Number 174 (Monday, September 11, 2023)]
[Notices]
[Pages 62397-62398]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-19536]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
[OMB Number 1117-0013]
Agency Information Collection Activities; Proposed eCollection
eComments Requested; Extension of a Previously Approved Collection;
Application for Permit To Import Controlled Substances for Domestic
and/or Scientific Purposes
AGENCY: Drug Enforcement Administration, Department of Justice.
ACTION: 60-Day notice.
-----------------------------------------------------------------------
SUMMARY: The Drug Enforcement Administration (DEA), Department of
Justice (DOJ), will be submitting the following information collection
request to the Office of Management and Budget (OMB) for review and
approval in accordance with the Paperwork Reduction Act of 1995.
DATES: Comments are encouraged and will be accepted for 60 days until
November 13, 2023.
FOR FURTHER INFORMATION CONTACT: If you have additional comments
especially on the estimated public burden or associated response time,
suggestions, or need a copy of the proposed information collection
instrument with instructions or additional information, please contact
Scott A. Brinks, Regulatory Drafting and Policy Support Section, Drug
Enforcement Administration; Mailing Address: 8701 Morrissette Drive,
Springfield, Virginia 22152; Telephone: (571) 362-3261, Email:
[email protected].
SUPPLEMENTARY INFORMATION: Written comments and suggestions from the
public and affected agencies concerning the proposed collection of
information are encouraged. Your comments should address one or more of
the following four points:
--Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the Bureau of Justice
Statistics, including whether the information will have practical
utility;
--Evaluate the accuracy of the agency's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used;
--Evaluate whether and if so how the quality, utility, and clarity of
the information to be collected can be enhanced; and
--Minimize the burden of the collection of information on those who are
to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submission of responses.
Abstract: Section 1002 of the Controlled Substances Import and
Export Act (CSIEA) (21 U.S.C. 952) and Title 21, Code of Federal
Regulations 21 CFR, sections 1312.11, 1312.12 and 1312.13 requires any
person who desires to import controlled substances listed in schedules
I or II, any narcotic substance listed in schedules III or IV, or any
non-narcotic substance in schedule III which the Administrator has
specifically designated by regulation in section 1312.30, or any
nonnarcotic
[[Page 62398]]
substance in schedule IV or V which is also listed in schedule I or II
of the Convention on Psychotropic Substances, must have an import
permit. To obtain the permit to import controlled substances for
domestic and or scientific purposes, an application for the permit must
be made to the DEA, on DEA Form 357.
Overview of This Information Collection
1. Type of Information Collection: Extension of a previously
approved collection.
2. The Title of the Form/Collection: Application for Permit to
Import Controlled Substances for Domestic and/or Scientific Purposes.
3. The agency form number, if any, and the applicable component of
the Department sponsoring the collection: DEA Form 357. The applicable
component within the Department of Justice is the Drug Enforcement
Administration, Office of Diversion Control.
4. Affected public who will be asked or required to respond, as
well as the obligation to respond: Affected Public: Private Sector--
businesses or other for-profit institutions. The obligation to respond
is mandatory per 21 CFR, sections 1312.11, 1312.12 and 1312.13.
5. An estimate of the total number of respondents and the amount of
time estimated for an average respondent to respond: The DEA estimates
that 124 registrants participate in this information collection. The
time per response is 21 minutes to complete the DEA-357 (paper) and 15
minutes to complete DEA-357 (online).
6. An estimate of the total annual burden (in hours) associated
with the collection: DEA estimates that this collection takes 264.35
annual burden hours.
7. An estimate of the total annual cost burden associated with the
collection, if applicable: $0.
Total Burden Hours
----------------------------------------------------------------------------------------------------------------
Time per
Activity Number of Frequency Total annual response Total annual
respondents responses (min.) burden (hours)
----------------------------------------------------------------------------------------------------------------
DEA Form: 357 (online).......... 124 9 958 15 266
DEA Form: 357 (paper)........... 71 21 19
-------------------------------------------------------------------------------
Unduplicated Totals......... 124 .............. 1,081 0.26 264.35
----------------------------------------------------------------------------------------------------------------
If additional information is required contact: Darwin Arceo,
Department Clearance Officer, United States Department of Justice,
Justice Management Division, Policy and Planning Staff, Two
Constitution Square, 145 N Street NE, 4W-218, Washington, DC.
Dated: September 5, 2023.
Darwin Arceo,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2023-19536 Filed 9-8-23; 8:45 am]
BILLING CODE 4410-09-P