Agency Information Collection Activities: Proposed eCollection, eComments Requested; Reinstatement of a Discontinued Collection: Recordkeeping for Electronic Prescriptions for Controlled Substances, 46016-46017 [2021-17523]
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46016
Federal Register / Vol. 86, No. 156 / Tuesday, August 17, 2021 / Notices
DEPARTMENT OF JUSTICE
Bureau of Alcohol, Tobacco, Firearms
and Explosives
[OMB Number 1140–0087]
Agency Information Collection
Activities; Proposed eCollection of
eComments Requested; Extension
Without Change of a Currently
Approved Collection; eForm Access
Request/User Registration
Bureau of Alcohol, Tobacco,
Firearms and Explosives, Department of
Justice.
ACTION: 30-Day notice.
AGENCY:
The Bureau of Alcohol,
Tobacco, Firearms and Explosives
(ATF), Department of Justice (DOJ) will
submit 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 an additional 30
days until September 16, 2021.
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 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.,
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SUMMARY:
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permitting electronic submission of
responses.
Overview of This Information
Collection
(1) Type of Information Collection:
Extension without change of a currently
approved collection.
(2) The Title of the Form/Collection:
eForm Access Request/User
Registration.
(3) The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
Form number: 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 a brief
abstract:
Primary: Business or other for profit.
Other: None.
Abstract: Members of the public will
use the eForm Access Request/User
Registration to create a username and
password for access to the Bureau of
Alcohol, Tobacco, Firearms, and
Explosives’ (ATF’s) eForms platform,
which is an electronic application filing
system.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: An estimated 76,000
respondents will complete this
registration form annually, and it will
take each respondent approximately
2.24 minutes to complete their
responses.
(6) An estimate of the total public
burden (in hours) associated with the
collection: The estimated annual public
burden associated with this collection is
2,387 hours, which is equal to 76,000 (#
of respondents) * .037333333 (2.24
minutes).
If additional information is required
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, Mail Stop
3E.405A, Washington, DC 20530.
Dated: August 12, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2021–17611 Filed 8–16–21; 8:45 am]
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DEPARTMENT OF JUSTICE
[OMB Number 1117–0049]
Agency Information Collection
Activities: Proposed eCollection,
eComments Requested; Reinstatement
of a Discontinued Collection:
Recordkeeping for Electronic
Prescriptions for Controlled
Substances
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
October 18, 2021.
FOR FURTHER INFORMATION CONTACT: If
you have comments 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, Diversion Control
Division, Drug Enforcement
Administration; Mailing Address: 8701
Morrissette Drive, Springfield, Virginia
22152; Telephone: (571) 362–3261.
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.
SUMMARY:
E:\FR\FM\17AUN1.SGM
17AUN1
46017
Federal Register / Vol. 86, No. 156 / Tuesday, August 17, 2021 / Notices
Overview of This Information
Collection
1. Type of Information Collection:
Reinstatement of a discontinued
collection.
2. Title of the Form/Collection:
Recordkeeping for Electronic
Prescriptions for Controlled Substance.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
There is no form number. 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: DEA is requiring that each
registered practitioner apply to an
approved credential service provider
approved to obtain identity proofing
and a credential. Hospitals and other
institutional practitioners may conduct
this process in-house as part of their
credentialing. For practitioners
currently working at or affiliated with a
registered hospital or clinic, the
hospital/clinic have to check a
government-issued photographic
identification. This may be done when
the hospital/clinic issues credentials to
new hires or newly affiliated
physicians. For individual practitioners,
two people need to enter logical access
control data to grant permissions for
practitioners authorized to approve and
sign controlled substance prescriptions
using the electronic prescription
application. For institutional
practitioners, logical access control data
is entered by two people from an entity
within the hospital/clinic that is
separate from the entity that conduct
identity proofing in-house. Similarly,
pharmacies have to set logical access
controls in the pharmacy application so
that only authorized employees have
permission to annotate or alter
prescription records. Finally, if the
electronic prescription or pharmacy
application generates an incident report,
practitioners, hospitals/clinics, and
pharmacies have to review the incident
report to determine if the event
identified by the application represents
a security incident.
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, hour burden per responses
and associated burden hours.
Number of
respondents
Burden
hours
Practitioners .................................................................................................................................
MLP ..............................................................................................................................................
Hospital/Clinics ............................................................................................................................
Pharmacies ..................................................................................................................................
78,164
49,067
1,482
3,984
0.67
0.67
2.13
0.33
52,370
32,875
3,157
1,315
Total ......................................................................................................................................
132,697
........................
89,717
6. An estimate of the total public
burden (in hours) associated with the
proposed collection: DEA estimates that
this collection takes 89,717 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 11, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2021–17523 Filed 8–16–21; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF LABOR
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Hour burden
per response
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request;
Respiratory Protection Standard
Notice of availability; request
for comments.
ACTION:
The Department of Labor
(DOL) is submitting this Occupational
SUMMARY:
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Safety and Health Administration
(OSHA)-sponsored information
collection request (ICR) to the Office of
Management and Budget (OMB) for
review and approval in accordance with
the Paperwork Reduction Act of 1995
(PRA). Public comments on the ICR are
invited.
DATES: The OMB will consider all
written comments that agency receives
on or before September 16, 2021.
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.
Comments are invited on: (1) Whether
the collection of information is
necessary for the proper performance of
the functions of the Department,
including whether the information will
have practical utility; (2) if the
information will be processed and used
in a timely manner; (3) the accuracy of
the agency’s estimates of the burden and
cost of the collection of information,
including the validity of the
methodology and assumptions used; (4)
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ways to enhance the quality, utility and
clarity of the information collection; and
(5) ways to minimize the burden of the
collection of information on those who
are to respond, including the use of
automated collection techniques or
other forms of information technology.
FOR FURTHER INFORMATION CONTACT:
Crystal Rennie by telephone at 202–
693–0456 or by email at DOL_PRA_
PUBLIC@dol.gov.
SUPPLEMENTARY INFORMATION: This
standard requires employers to develop
a written respiratory protection
program, provide medical surveillance,
fit test employees, obtain certificates of
analysis on cylinders, change sorbent
beds and filters, to inspect emergencyuse respirators, mark emergency-use
respirator storage compartments, and
maintain accurate employee records for
fit testing and medical surveillance. For
additional substantive information
about this ICR, see the related notice
published in the Federal Register on
April 9, 2021 (86 FR 18557).
This information collection is subject
to the PRA. A Federal agency generally
cannot conduct or sponsor a collection
of information, and the public is
generally not required to respond to an
information collection, unless the OMB
approves it and displays a currently
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]]>Agencies
[Federal Register Volume 86, Number 156 (Tuesday, August 17, 2021)]
[Notices]
[Pages 46016-46017]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-17523]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
[OMB Number 1117-0049]
Agency Information Collection Activities: Proposed eCollection,
eComments Requested; Reinstatement of a Discontinued Collection:
Recordkeeping for Electronic Prescriptions for Controlled Substances
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
October 18, 2021.
FOR FURTHER INFORMATION CONTACT: If you have comments 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, Diversion
Control Division, Drug Enforcement Administration; Mailing Address:
8701 Morrissette Drive, Springfield, Virginia 22152; Telephone: (571)
362-3261.
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.
[[Page 46017]]
Overview of This Information Collection
1. Type of Information Collection: Reinstatement of a discontinued
collection.
2. Title of the Form/Collection: Recordkeeping for Electronic
Prescriptions for Controlled Substance.
3. The agency form number, if any, and the applicable component of
the Department sponsoring the collection: There is no form number. 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: DEA is requiring that each registered practitioner apply
to an approved credential service provider approved to obtain identity
proofing and a credential. Hospitals and other institutional
practitioners may conduct this process in-house as part of their
credentialing. For practitioners currently working at or affiliated
with a registered hospital or clinic, the hospital/clinic have to check
a government-issued photographic identification. This may be done when
the hospital/clinic issues credentials to new hires or newly affiliated
physicians. For individual practitioners, two people need to enter
logical access control data to grant permissions for practitioners
authorized to approve and sign controlled substance prescriptions using
the electronic prescription application. For institutional
practitioners, logical access control data is entered by two people
from an entity within the hospital/clinic that is separate from the
entity that conduct identity proofing in-house. Similarly, pharmacies
have to set logical access controls in the pharmacy application so that
only authorized employees have permission to annotate or alter
prescription records. Finally, if the electronic prescription or
pharmacy application generates an incident report, practitioners,
hospitals/clinics, and pharmacies have to review the incident report to
determine if the event identified by the application represents a
security incident.
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, hour burden
per responses and associated burden hours.
----------------------------------------------------------------------------------------------------------------
Number of Hour burden
respondents per response Burden hours
----------------------------------------------------------------------------------------------------------------
Practitioners................................................... 78,164 0.67 52,370
MLP............................................................. 49,067 0.67 32,875
Hospital/Clinics................................................ 1,482 2.13 3,157
Pharmacies...................................................... 3,984 0.33 1,315
-----------------------------------------------
Total....................................................... 132,697 .............. 89,717
----------------------------------------------------------------------------------------------------------------
6. An estimate of the total public burden (in hours) associated
with the proposed collection: DEA estimates that this collection takes
89,717 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 11, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2021-17523 Filed 8-16-21; 8:45 am]
BILLING CODE 4410-09-P
