Agency Information Collection Activities; Proposed eCollection, eComments Requested; Extension Without Change of a Previously Approved Collection; Reports of Loss or Disappearance of Listed Chemicals and Regulated Transactions in Tableting/Encapsulating Machines; DEA Forms 107 and 452, 48268-48269 [2020-17376]
Download as PDF
48268
Federal Register / Vol. 85, No. 154 / Monday, August 10, 2020 / Notices
—Evaluate whether and if so how the
quality, utility, and clarity of the
information proposed 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 forms of
information technology, e.g.,
permitting electronic submission of
responses.
Department Clearance Officer, United
States Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street NE, Suite 3E.405B,
Washington, DC 20530.
Dated: August 5, 2020.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2020–17379 Filed 8–7–20; 8:45 am]
jbell on DSKJLSW7X2PROD with NOTICES
BILLING CODE 4410–09–P
Overview of This Information
Collection
1. Type of Information Collection:
Extension of a currently approved
collection.
2. Title of the Form/Collection:
Application for Permit to Export
Controlled Substances; Application for
Permit to Export Controlled Substances
for Subsequent Re-export.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
DEA Forms: 161, 161R, 161R–EEA. The
applicable component within the
Department of Justice is the Drug
Enforcement Administration, Diversion
Control Division.
4. Affected public who will be asked
or required to respond, as well as a brief
abstract:
Affected public (Primary): Business or
other for-profit.
Affected public (Other): Not-for-profit
institutions; Federal, State, local, and
tribal governments.
Abstract: Title 21, Code of Federal
Regulations (21 CFR), Sections 1312.21
and 1312.22 require that any person
who desires to export or re-export
controlled substances listed in
schedules I or II, any narcotic substance
listed in schedules III or IV, or any nonnarcotic substance in schedule III which
the Administrator has specifically
designated by regulation in § 1312.30, or
any non-narcotic substance in schedules
IV or V which is also listed in schedule
I or II of the Convention on
Psychotropic Substances, must have an
export permit.
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 127
respondents, with 7,282 responses
annually to this collection. The DEA
estimates that it takes .52719 hour to
complete the form.
6. An estimate of the total public
burden (in hours) associated with the
proposed collection: The DEA estimates
that this collection takes 3,839 annual
burden hours.
If additional information is required
please contact: Melody Braswell,
VerDate Sep<11>2014
20:31 Aug 07, 2020
Jkt 250001
DEPARTMENT OF JUSTICE
[OMB Number 1117–0024]
Agency Information Collection
Activities; Proposed eCollection,
eComments Requested; Extension
Without Change of a Previously
Approved Collection; Reports of Loss
or Disappearance of Listed Chemicals
and Regulated Transactions in
Tableting/Encapsulating Machines;
DEA Forms 107 and 452
Drug Enforcement
Administration, Department of Justice.
ACTION: 30-Day notice.
AGENCY:
The Department of Justice
(DOJ), Drug Enforcement
Administration (DEA), 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.
This proposed information collection
was previously published in the Federal
Register on June 03, 2020, allowing for
a 60 day comment period.
DATES: Comments are encouraged and
will be accepted for an additional 30
days until September 9, 2020.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
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 agency, including
SUMMARY:
PO 00000
Frm 00120
Fmt 4703
Sfmt 4703
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 proposed 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 forms of
information technology, e.g.,
permitting electronic submission of
responses.
Overview of This Information
Collection
1. Type of Information Collection:
Extension of a currently approved
collection.
2. Title of the Form/Collection:
Reports of Loss or Disappearance of
Listed Chemicals and Regulated
Transactions in Tableting/Encapsulating
Machines.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
DEA Forms 107 and 452. The applicable
component within the Department of
Justice is the Drug Enforcement
Administration, Diversion Control
Division.
4. Affected public who will be asked
or required to respond, as well as a brief
abstract:
Affected public (Primary): Business or
other for-profit.
Affected public (Other): Not-for-profit
institutions; Federal, State, local, and
tribal governments.
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).
E:\FR\FM\10AUN1.SGM
10AUN1
Federal Register / Vol. 85, No. 154 / Monday, August 10, 2020 / Notices
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: DEA estimates that 2,331
persons respond as needed to this
collection. Responses take 20 minutes.
6. An estimate of the total public
burden (in hours) associated with the
proposed collection: DEA estimates that
this collection takes 1,276 annual
burden hours.
If additional information is required
please contact: Melody Braswell,
Department Clearance Officer, United
States Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street NE, Suite 3E.405B,
Washington, DC 20530.
Dated: August 5, 2020.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2020–17376 Filed 8–7–20; 8:45 am]
BILLING CODE 4410&ndash09–P
DEPARTMENT OF JUSTICE
[OMB Number 1117–0023]
Agency Information Collection
Activities; Proposed eCollection,
eComments Requested; Extension
Without Change of a Previously
Approved Collection; Import/Export
Declaration for List I and List II
Chemicals; DEA Forms 486, 486A
Drug Enforcement
Administration, Department of Justice.
AGENCY:
ACTION:
30-Day notice.
The Department of Justice
(DOJ), Drug Enforcement
Administration (DEA), 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.
SUMMARY:
Comments are encouraged and
will be accepted for 30 days until
September 9, 2020.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
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 agency, 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 proposed 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 forms of
information technology, e.g.,
permitting electronic submission of
responses.
DATES:
Overview of This Information
Collection
1. Type of Information Collection:
Extension of a currently approved
collection.
2. Title of the Form/Collection:
Import/Export Declaration for List I and
List II Chemicals.
jbell on DSKJLSW7X2PROD with NOTICES
Number of
annual
respondents
Number of
annual
responses
48269
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, Diversion Control
Division.
4. Affected public who will be asked
or required to respond, as well as a brief
abstract:
Affected public (Primary): Business or
other for-profit.
Affected public (Other): Not-for-profit
institutions; Federal, State, local, and
tribal governments.
Abstract: Section 1018 of the
Controlled Substances Import and
Export Act (CSIEA) (21 U.S.C. 971) and
Title 21 Code of Federal Regulations (21
CFR) part 1313 require any persons who
import, export, or conduct international
transactions involving list I and list II
chemicals are required to establish a
system of recordkeeping and report
certain information regarding those
transactions to DEA. The chemicals
subject to control are used in the
clandestine manufacture of controlled
substances. The reports of domestic,
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.
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: The below table presents
information regarding the number of
respondents, responses and associated
burden hours.
Average time per response
(hours)
DEA–486—Import ...................................................................
DEA–486—Export ...................................................................
DEA–486—International .........................................................
DEA–486A—Import .................................................................
132
227
20
38
2,153
13,142
424
697
0.33
0.28
0.28
0.40
...................
...................
...................
...................
718
3,724
120
279
Total .................................................................................
417
16,416
.................................................
4,840
6. An estimate of the total public
burden (in hours) associated with the
proposed collection: DEA estimates that
VerDate Sep<11>2014
20:31 Aug 07, 2020
Jkt 250001
this collection takes 4,840 annual
burden hours.
If additional information is required
please contact: Melody Braswell,
PO 00000
Frm 00121
Fmt 4703
Sfmt 4703
(20
(17
(17
(24
minutes)
minutes)
minutes)
minutes)
Total annual
hours
Department Clearance Officer, United
States Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
E:\FR\FM\10AUN1.SGM
10AUN1
Agencies
[Federal Register Volume 85, Number 154 (Monday, August 10, 2020)]
[Notices]
[Pages 48268-48269]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-17376]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
[OMB Number 1117-0024]
Agency Information Collection Activities; Proposed eCollection,
eComments Requested; Extension Without Change of a Previously Approved
Collection; Reports of Loss or Disappearance of Listed Chemicals and
Regulated Transactions in Tableting/Encapsulating Machines; DEA Forms
107 and 452
AGENCY: Drug Enforcement Administration, Department of Justice.
ACTION: 30-Day notice.
-----------------------------------------------------------------------
SUMMARY: The Department of Justice (DOJ), Drug Enforcement
Administration (DEA), 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. This proposed information collection was previously published in
the Federal Register on June 03, 2020, allowing for a 60 day comment
period.
DATES: Comments are encouraged and will be accepted for an additional
30 days until September 9, 2020.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
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 agency, 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 proposed 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 forms of information technology, e.g.,
permitting electronic submission of responses.
Overview of This Information Collection
1. Type of Information Collection: Extension of a currently
approved collection.
2. Title of the Form/Collection: Reports of Loss or Disappearance
of Listed Chemicals and Regulated Transactions in Tableting/
Encapsulating Machines.
3. The agency form number, if any, and the applicable component of
the Department sponsoring the collection: DEA Forms 107 and 452. The
applicable component within the Department of Justice is the Drug
Enforcement Administration, Diversion Control Division.
4. Affected public who will be asked or required to respond, as
well as a brief abstract:
Affected public (Primary): Business or other for-profit.
Affected public (Other): Not-for-profit institutions; Federal,
State, local, and tribal governments.
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).
[[Page 48269]]
5. An estimate of the total number of respondents and the amount of
time estimated for an average respondent to respond: DEA estimates that
2,331 persons respond as needed to this collection. Responses take 20
minutes.
6. An estimate of the total public burden (in hours) associated
with the proposed collection: DEA estimates that this collection takes
1,276 annual burden hours.
If additional information is required please contact: Melody
Braswell, Department Clearance Officer, United States Department of
Justice, Justice Management Division, Policy and Planning Staff, Two
Constitution Square, 145 N Street NE, Suite 3E.405B, Washington, DC
20530.
Dated: August 5, 2020.
Melody Braswell,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2020-17376 Filed 8-7-20; 8:45 am]
BILLING CODE 4410&ndash09-P