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
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.