Proposed Data Collection Submitted for Public Comment and Recommendations, 60047-60048 [2021-23556]
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60047
Federal Register / Vol. 86, No. 207 / Friday, October 29, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
Cruise ship physician ....................
Cruise COVID–19 Contact Investigation Worksheet (if
necessary).
Approval of Onboard COVID–19 Testing Instrument ......
Mass Crew Testing Requirement ....................................
Agreement with Health Care Organization with signoff
from Local Health Authorities.
Agreement with Port of Entry with signoff from Local
Health Authority.
Agreement with Housing Facility with signoff from Local
Health Authority.
Request for Approval to Conduct a Simulated Voyage
Prior to Issuance of COVID–19 Conditional Sailing
Certificate.
Informed Consent and Medical Certification with no preexisting conditions for Simulated Voyage.
Remote and In-person Inspections ..................................
After Action Report, Simulated Voyage ...........................
COVID–19 Conditional Sailing Certificate Application .....
Remote and In-person Inspections ..................................
Cruise ship brand/operator ...........
Cruise ship brand/operator ...........
Cruise ship brand/operator ...........
Cruise ship brand/operator ...........
Cruise ship brand/operator ...........
Cruise ship operator .....................
Passenger (3rd party disclosure) ..
Cruise
Cruise
Cruise
Cruise
ship
ship
ship
ship
operator
operator
operator
operator
.....................
.....................
.....................
.....................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–23555 Filed 10–28–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–0017; Docket No. CDC–2021–
0116]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Application for Training, which
supports the management and
evaluation of online training and
professional development opportunities
for public health and health care
professionals.
SUMMARY:
khammond on DSKJM1Z7X2PROD with NOTICES
Number of
respondents
Type of respondent
VerDate Sep<11>2014
18:17 Oct 28, 2021
Jkt 256001
CDC must receive written
comments on or before December 28,
2021.
DATES:
You may submit comments,
identified by Docket No. CDC–2021–
0116 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
ADDRESSES:
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
Number
responses per
respondent
Average
burden per
response
(in hrs.)
24
1
30/60
60
60
60
1
1
1
60/60
5/60
600/60
60
1
600/60
60
1
600/60
30
1
600/60
18,000
1
15/60
30
30
60
130
1
1
1
2
120/60
600/60
600/60
120/60
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. 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;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Application for Training—(OMB
Control No. 0920–0017, Exp. 04/30/
2022)—Revision—Center for
Surveillance, Epidemiology, and
E:\FR\FM\29OCN1.SGM
29OCN1
60048
Federal Register / Vol. 86, No. 207 / Friday, October 29, 2021 / Notices
Laboratory Services (CSELS), Division
of Scientific Education and Professional
Development (DSEPD), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC requests OMB approval for the
Revision of a currently approved
Information Collection Request (ICR)
titled Application for Training (OMB
Control No. 0920–0017). The mission of
CDC’s Division of Scientific Education
and Professional Development (DSEPD)
is to support the development of a
competent, sustainable, and empowered
public health workforce. Professionals
in public health, epidemiology,
medicine, economics, information
science, veterinary medicine, nursing,
public policy, and other related
professions, seek professional
development opportunities (both
accredited and nonaccredited) through
two CDC learning management systems.
These two learning management
systems are Training and Continuing
Education Online (TCEO) (for
accredited courses) and CDC TRAIN (for
nonaccredited courses developed by
CDC programs, grantees, and other
funded partners). Access to quality and
accredited learning programs and
products through these two systems
allow for the public health workforce to
courses based on learner feedback. At
this time, TCEO is also used to generate
certificates of attendance and verify
training completion, review and
approve proposals for educational
activities to receive continuing
education accreditation, and ensure
compliance with mandatory
accreditation standards.
broaden their knowledge and skills to
improve the science and practice of
public health for domestic and
international impact.
The overarching purpose of this ICR
is to continually improve CDC training
activities and maintain CDC compliance
with mandatory accreditation
organization standards by efficiently
collecting information through CDC’s
Training and Continuing Education
Online (TCEO) and CDC TRAIN
systems, while navigating a future
merger that moves to using only one
system (CDC TRAIN). This revision
requests to extend current approval of
the TCEO forms, with one minor
change, namely to add two new
response options for one question on the
TCEO New Participant Registration.
This revision also requests to add CDC
TRAIN as a data collection system and
add two CDC TRAIN standard training
evaluation tools (one immediately after
the course is taken, and one 3–6 months
after the course is taken) that will be
employed on the learning management
system. This proposed change will
provide CDC with an efficient, effective,
and secure electronic mechanism for
collecting, processing, and monitoring
training-related information.
CDC will use information collected in
both systems to evaluate and improve
All data will be collected online,
using secure electronic web-based
password protected platforms.
Respondents will include educational
developers requesting accreditation for
their trainings and public health and
healthcare professionals who seek
training. No statistical methods will be
used to analyze the information
collected. CDC will use identifiable
information in TCEO to track
participant completion of educational
activities to facilitate required reporting
to earn continuing education credits,
hours, or units. Aggregate and nonaggregate data from the evaluations in
TCEO and CDC TRAIN will be used to
improve educational activities and
assess learning outcomes.
CDC requests OMB approval for an
estimated 412,600 annual burden hours.
There are no costs to respondents other
than their time to participate.
khammond on DSKJM1Z7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden time
per response
(in hours)
Total response
burden
(in hours)
Type of respondents
Form name
Educational Developers (Health Educators)
Public Health and Health Care Professionals (Learners).
Public Health and Health Care Professionals (Learners).
Public Health and Health Care Professionals (Learners).
TCEO Proposal ....................
TCEO New Participant Registration.
TCEO Post-Course Evaluation.
TCEO Follow-up Evaluation
120
300,000
1
1
5
5/60
600
25,000
300,000
3
10/60
150,000
30,000
3
3/60
4,500
TCEO Sub-Total ....................................
...............................................
........................
........................
........................
180,100
Public Health and Health Care Professionals (Learners).
Public Health and Health Care Professionals (Learners).
CDC TRAIN Immediate PostCourse Evaluation Tool.
CDC TRAIN Delayed FollowUp Evaluation Tool.
300,000
3
15/60
225,000
30,000
3
5/60
7,500
0.33TRAIN Sub-Total ............................
...............................................
........................
........................
........................
232,500
Total ................................................
...............................................
........................
........................
........................
412,600
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–23556 Filed 10–28–21; 8:45 am]
BILLING CODE 4163–18–P
VerDate Sep<11>2014
18:17 Oct 28, 2021
Jkt 256001
PO 00000
Frm 00073
Fmt 4703
Sfmt 4703
E:\FR\FM\29OCN1.SGM
29OCN1
]]>Agencies
[Federal Register Volume 86, Number 207 (Friday, October 29, 2021)]
[Notices]
[Pages 60047-60048]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-23556]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-22-0017; Docket No. CDC-2021-0116]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Application for Training, which
supports the management and evaluation of online training and
professional development opportunities for public health and health
care professionals.
DATES: CDC must receive written comments on or before December 28,
2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0116 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
[email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. 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;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. 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
submissions of responses; and
5. Assess information collection costs.
Proposed Project
Application for Training--(OMB Control No. 0920-0017, Exp. 04/30/
2022)--Revision--Center for Surveillance, Epidemiology, and
[[Page 60048]]
Laboratory Services (CSELS), Division of Scientific Education and
Professional Development (DSEPD), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC requests OMB approval for the Revision of a currently approved
Information Collection Request (ICR) titled Application for Training
(OMB Control No. 0920-0017). The mission of CDC's Division of
Scientific Education and Professional Development (DSEPD) is to support
the development of a competent, sustainable, and empowered public
health workforce. Professionals in public health, epidemiology,
medicine, economics, information science, veterinary medicine, nursing,
public policy, and other related professions, seek professional
development opportunities (both accredited and nonaccredited) through
two CDC learning management systems. These two learning management
systems are Training and Continuing Education Online (TCEO) (for
accredited courses) and CDC TRAIN (for nonaccredited courses developed
by CDC programs, grantees, and other funded partners). Access to
quality and accredited learning programs and products through these two
systems allow for the public health workforce to broaden their
knowledge and skills to improve the science and practice of public
health for domestic and international impact.
The overarching purpose of this ICR is to continually improve CDC
training activities and maintain CDC compliance with mandatory
accreditation organization standards by efficiently collecting
information through CDC's Training and Continuing Education Online
(TCEO) and CDC TRAIN systems, while navigating a future merger that
moves to using only one system (CDC TRAIN). This revision requests to
extend current approval of the TCEO forms, with one minor change,
namely to add two new response options for one question on the TCEO New
Participant Registration. This revision also requests to add CDC TRAIN
as a data collection system and add two CDC TRAIN standard training
evaluation tools (one immediately after the course is taken, and one 3-
6 months after the course is taken) that will be employed on the
learning management system. This proposed change will provide CDC with
an efficient, effective, and secure electronic mechanism for
collecting, processing, and monitoring training-related information.
CDC will use information collected in both systems to evaluate and
improve courses based on learner feedback. At this time, TCEO is also
used to generate certificates of attendance and verify training
completion, review and approve proposals for educational activities to
receive continuing education accreditation, and ensure compliance with
mandatory accreditation standards.
All data will be collected online, using secure electronic web-
based password protected platforms. Respondents will include
educational developers requesting accreditation for their trainings and
public health and healthcare professionals who seek training. No
statistical methods will be used to analyze the information collected.
CDC will use identifiable information in TCEO to track participant
completion of educational activities to facilitate required reporting
to earn continuing education credits, hours, or units. Aggregate and
non-aggregate data from the evaluations in TCEO and CDC TRAIN will be
used to improve educational activities and assess learning outcomes.
CDC requests OMB approval for an estimated 412,600 annual burden
hours. There are no costs to respondents other than their time to
participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average burden
Number of Number of time per Total response
Type of respondents Form name respondents responses per response (in burden (in
respondent hours) hours)
----------------------------------------------------------------------------------------------------------------
Educational Developers (Health TCEO Proposal... 120 1 5 600
Educators).
Public Health and Health Care TCEO New 300,000 1 5/60 25,000
Professionals (Learners). Participant
Registration.
Public Health and Health Care TCEO Post-Course 300,000 3 10/60 150,000
Professionals (Learners). Evaluation.
Public Health and Health Care TCEO Follow-up 30,000 3 3/60 4,500
Professionals (Learners). Evaluation.
---------------------------------------------------------------
TCEO Sub-Total............ ................ .............. .............. .............. 180,100
===============================================================
Public Health and Health Care CDC TRAIN 300,000 3 15/60 225,000
Professionals (Learners). Immediate Post-
Course
Evaluation Tool.
Public Health and Health Care CDC TRAIN 30,000 3 5/60 7,500
Professionals (Learners). Delayed Follow-
Up Evaluation
Tool.
---------------------------------------------------------------
0.33TRAIN Sub-Total....... ................ .............. .............. .............. 232,500
===============================================================
Total................. ................ .............. .............. .............. 412,600
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-23556 Filed 10-28-21; 8:45 am]
BILLING CODE 4163-18-P
