Agency Information Collection Activities; Proposed eCollection eComments Requested; New Information Collection Request; Emergency Medical Services Recordkeeping and Notice Requirements, 81110-81111 [2024-23091]
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81110
Federal Register / Vol. 89, No. 194 / Monday, October 7, 2024 / Notices
TOTAL BURDEN HOURS
Number of
respondents
Activity
Time per response
(hours)
Total annual
burden
(hours)
DEA—224 .......................................................
DEA—224A .....................................................
146,285
524,196
........................
........................
0.33 hours (20 minutes) .................................
0.17 hours (10 minutes) .................................
48,762
87,366
Unduplicated Totals .................................
670,481
........................
.........................................................................
136,366
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 20530.
Dated: October 1, 2024.
Darwin Arceo,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2024–23027 Filed 10–4–24; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
[OMB Number 1117–0060]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; New
Information Collection Request;
Emergency Medical Services
Recordkeeping and Notice
Requirements
Drug Enforcement
Administration, Department of Justice.
ACTION: 60-Day notice.
AGENCY:
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
December 6, 2024.
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
Heather E. Achbach, Regulatory Drafting
and Policy Support Section, Drug
Enforcement Administration; Mailing
Address: 8701 Morrissette Drive,
Springfield, Virginia 22152; Telephone:
(571) 776–3882; Email: DEA.PRA@
dea.gov or Heather.E.Achbach@dea.gov.
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Total annual
responses
VerDate Sep<11>2014
17:11 Oct 04, 2024
Jkt 262001
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: The Controlled Substances
Act (CSA) (21 U.S.C. 801–971) requires
all persons who handle controlled
substances to obtain a registration from
the Attorney General. 21 U.S.C. 822,
823, 831, 957, and 958. The ‘‘Protecting
Patient Access to Emergency
Medications Act of 2017,’’ (hereafter the
‘‘Act’’) which became law on November
17, 2017, amended the Controlled
Substances Act to allow for a new
registration category for emergency
medical services agencies that handle
controlled substances. It also
established standards for registering
emergency medical services agencies,
and set forth new requirements for
delivery, storage, and recordkeeping
related to their handling of controlled
substances.
With this proposed collection, DEA is
proposing recordkeeping regulations for
EMS agencies to incorporate the Act’s
CSA amendments regarding
recordkeeping, and to ensure an
accurate accounting of the controlled
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
substances outside the two-registrant
integrity system.
The Act require EMS agencies to
maintain records of the EMS personnel
whose State license or certification gives
them the ability to administer controlled
substances, in compliance with their
State laws. Under 21 U.S.C 827(b),
controlled substance records for all DEA
registrants are required to be maintained
for at least two years from the date of
such inventory or records. Following
the Act, 21 U.S.C. 823(k)(9)(B)(ii), DEA
would require that records be
maintained, whether electronically or
otherwise, at each registered and
designated location of the agency where
the controlled substances involved are
received, administered, or otherwise
disposed of.
Consistent with the Act’s
amendments to the CSA, 21 U.S.C.
823(k)(9), DEA would require an EMS
agency to maintain records for each
controlled substance administered or
disposed of in the course of providing
emergency medical services. In
addition, any EMS personnel who
disposes of or administers controlled
substances to a patient in the course of
providing emergency medical care
would have to record the name of the
controlled substance(s) and detailed
information about the circumstances
surrounding the administration of the
controlled substance(s) (e.g., name of
the substance, date dispensed,
identification of the patient).
Additionally, in accordance with 21
U.S.C 821(k)(9)(b), that an EMS agency
must maintain records of controlled
substances delivered between registered
and designated locations of the agency
(except agencies restocking at the
hospital under which the EMS agency is
operating, because the hospital is
required to keep records of such
restocking). These records, for example,
should include the name of the
controlled substance(s), finished form,
number of units in the commercial
container, date delivered, and the
address of the EMS agency location
where the controlled substances were
delivered.
E:\FR\FM\07OCN1.SGM
07OCN1
81111
Federal Register / Vol. 89, No. 194 / Monday, October 7, 2024 / Notices
Overview of This information
Collection
1. Type of Information Collection:
New information collection.
2. The Title of the Form/Collection:
Emergency Medical Services
Recordkeeping and Notice
Requirements.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
No form number is associated with this
collection. 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 the
obligation to respond: Affected Public:
(Primary) Business or other for-profit.
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 21,283
Registrants participate in this
information collection. The time per
response is 5 minutes.
6. An estimate of the total annual
burden (in hours) associated with the
collection: DEA Estimates that this
collection takes 92,226 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
Total annual
burden
(hours)
EMS Recordkeeping and Notice .........................................
21,283
52
1,106,716
5 min
92,226
Unduplicated Totals ......................................................
21,283
........................
1,106,716
........................
92,226
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: October 2, 2024.
Darwin Arceo,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2024–23091 Filed 10–4–24; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
[OMB 1140–0050]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Revision of a
Previously Approved Collection;
Identification Markings Placed on
Firearms
Bureau of Alcohol, Tobacco,
Firearms and Explosives, Department of
Justice.
ACTION: 60-Day notice.
AGENCY:
The Department of Justice
(DOJ), The Bureau of Alcohol, Tobacco,
Firearms and Explosives (ATF), 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
December 6, 2024.
FOR FURTHER INFORMATION CONTACT: If
you have additional comments
especially on the estimated public
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Frequency
VerDate Sep<11>2014
17:11 Oct 04, 2024
Jkt 262001
burden or associated response time,
suggestions, or need a copy of the
proposed information collection
instrument with instructions or
additional information, contact: Jennifer
Scott, FIPB, either by mail at Bureau of
Alcohol, Tobacco, Firearms, and
Explosives; 99 New York Ave.,
Washington, DC 20226, by email at fipbinformationcollection@atf.gov or
telephone at 202–648–7190.
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: Each licensed firearms
manufacturer and licensed firearms
importer must legibly identify each
PO 00000
Frm 00073
Fmt 4703
Sfmt 4703
firearm by engraving, casting, stamping
(impressing), or otherwise
conspicuously placing on the frame or
receiver an individual serial number,
any associated license number, and all
other additional required information to
a depth of at least .003 inch and in a
print size no smaller than 1⁄16 inch.
Used to facilitate the investigations of
the criminal use of firearms. Information
Collection (IC) OMB #1140–0050 is
being revised to reflect an increase in
costs resulting from an increase in the
number of respondents and firearms
covered by the information collection,
and from adding both a burden hour
monetized value and start-up costs
based on a rulemaking that occurred
since the last time this collection was
renewed.
Overview of This Information
Collection
1. Type of Information Collection:
Revision of a previously approved
collection.
2. The Title of the Form/Collection:
Identification Markings Placed on
Firearms.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
None.
Component: Bureau of Alcohol,
Tobacco, Firearms and Explosives, U.S.
Department of Justice.
4. Affected public who will be asked
or required to respond, as well as the
obligation to respond: Affected Public:
Private Sector-for or not for profit
institutions.
The obligation to respond is
mandatory per 18 U.S.C Chapter 44 and
26 U.S.C § 5842.
5. An estimate of the total number of
respondents and the amount of time
E:\FR\FM\07OCN1.SGM
07OCN1
Agencies
[Federal Register Volume 89, Number 194 (Monday, October 7, 2024)]
[Notices]
[Pages 81110-81111]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-23091]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
[OMB Number 1117-0060]
Agency Information Collection Activities; Proposed eCollection
eComments Requested; New Information Collection Request; Emergency
Medical Services Recordkeeping and Notice Requirements
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
December 6, 2024.
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
Heather E. Achbach, Regulatory Drafting and Policy Support Section,
Drug Enforcement Administration; Mailing Address: 8701 Morrissette
Drive, Springfield, Virginia 22152; Telephone: (571) 776-3882; Email:
[email protected] or [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: The Controlled Substances Act (CSA) (21 U.S.C. 801-971)
requires all persons who handle controlled substances to obtain a
registration from the Attorney General. 21 U.S.C. 822, 823, 831, 957,
and 958. The ``Protecting Patient Access to Emergency Medications Act
of 2017,'' (hereafter the ``Act'') which became law on November 17,
2017, amended the Controlled Substances Act to allow for a new
registration category for emergency medical services agencies that
handle controlled substances. It also established standards for
registering emergency medical services agencies, and set forth new
requirements for delivery, storage, and recordkeeping related to their
handling of controlled substances.
With this proposed collection, DEA is proposing recordkeeping
regulations for EMS agencies to incorporate the Act's CSA amendments
regarding recordkeeping, and to ensure an accurate accounting of the
controlled substances outside the two-registrant integrity system.
The Act require EMS agencies to maintain records of the EMS
personnel whose State license or certification gives them the ability
to administer controlled substances, in compliance with their State
laws. Under 21 U.S.C 827(b), controlled substance records for all DEA
registrants are required to be maintained for at least two years from
the date of such inventory or records. Following the Act, 21 U.S.C.
823(k)(9)(B)(ii), DEA would require that records be maintained, whether
electronically or otherwise, at each registered and designated location
of the agency where the controlled substances involved are received,
administered, or otherwise disposed of.
Consistent with the Act's amendments to the CSA, 21 U.S.C.
823(k)(9), DEA would require an EMS agency to maintain records for each
controlled substance administered or disposed of in the course of
providing emergency medical services. In addition, any EMS personnel
who disposes of or administers controlled substances to a patient in
the course of providing emergency medical care would have to record the
name of the controlled substance(s) and detailed information about the
circumstances surrounding the administration of the controlled
substance(s) (e.g., name of the substance, date dispensed,
identification of the patient).
Additionally, in accordance with 21 U.S.C 821(k)(9)(b), that an EMS
agency must maintain records of controlled substances delivered between
registered and designated locations of the agency (except agencies
restocking at the hospital under which the EMS agency is operating,
because the hospital is required to keep records of such restocking).
These records, for example, should include the name of the controlled
substance(s), finished form, number of units in the commercial
container, date delivered, and the address of the EMS agency location
where the controlled substances were delivered.
[[Page 81111]]
Overview of This information Collection
1. Type of Information Collection: New information collection.
2. The Title of the Form/Collection: Emergency Medical Services
Recordkeeping and Notice Requirements.
3. The agency form number, if any, and the applicable component of
the Department sponsoring the collection: No form number is associated
with this collection. 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 the obligation to respond: Affected Public: (Primary) Business
or other for-profit.
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 21,283 Registrants participate in this information collection. The
time per response is 5 minutes.
6. An estimate of the total annual burden (in hours) associated
with the collection: DEA Estimates that this collection takes 92,226
annual burden hours.
7. An estimate of the total annual cost burden associated with the
collection, if applicable: $0.
Total Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Total annual Time per Total annual
Activity respondents Frequency responses response burden (hours)
----------------------------------------------------------------------------------------------------------------
EMS Recordkeeping and Notice.... 21,283 52 1,106,716 5 min 92,226
-------------------------------------------------------------------------------
Unduplicated Totals......... 21,283 .............. 1,106,716 .............. 92,226
----------------------------------------------------------------------------------------------------------------
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: October 2, 2024.
Darwin Arceo,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2024-23091 Filed 10-4-24; 8:45 am]
BILLING CODE 4410-09-P