Agency Forms Undergoing Paperwork Reduction Act Review, 70164-70166 [2020-24475]
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70164
Federal Register / Vol. 85, No. 214 / Wednesday, November 4, 2020 / Notices
demonstrate impact and improve
implementation of OD2A. The purpose
of this information collection is to
assess the implementation and the
effectiveness of the OD2A program
activities and identify the conditions
under which these activities are most
effective, and for whom. The
implementation evaluation will identify
the barriers and facilitators associated
with deploying several prevention
activities targeting specific populations
within specific jurisdictions.
Data collected from this evaluation
will be used by the CDC to obtain valid
information regarding how recipients
operationalized and implemented their
chosen prevention activities, to assess
the impact of OD2A and different
components of OD2A on the trajectory
of the opioid epidemic, and through the
provision of these data back to the
recipients, to improve the
implementation and impact of further
OD2A prevention activities. There are
no costs to the respondents other than
their time. The total estimated
annualized burden hours are 574.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Jurisdictions implementing OD2A program ....
Key Informant Interview Guides .....................
Focus Group Guides ......................................
Permission to be Recorded ...........................
Interview Recruitment Email ..........................
Focus Group Recruitment Email ....................
Interview Recruitment Reminder Email .........
Focus Group Recruitment Reminder Email ...
Post-information Collection Follow up Email
Program Manager Focus Group Recruitment
Request Email.
Program Manager Interview Recruitment Request Email.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–24473 Filed 11–3–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–21–20OG]
Agency Forms Undergoing Paperwork
Reduction Act Review
khammond on DSKJM1Z7X2PROD with NOTICES
Number of
respondents
Type of respondent
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Assessments
of adults’ professional experiences for
improving programs to decrease sexual
risk and related behaviors and adverse
health outcomes among youth,’’ to the
Office of Management and Budget
(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on June 2, 2020 to obtain
comments from the public and affected
agencies. CDC did not receive comments
related to the previous notice. This
notice serves to allow an additional 30
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18:16 Nov 03, 2020
Jkt 253001
days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) 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;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
PO 00000
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Number of
responses per
respondent
Average
burden per
response
(hours )
181
165
346
181
165
181
165
346
165
1
1
1
1
1
1
1
1
1
1
1.5
5/60
5/60
5/60
5/60
5/60
5/60
5/60
181
1
5/60
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. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Assessments of adults’ professional
experiences for improving programs to
decrease sexual risk and related
behaviors and adverse health outcomes
among youth—New—Division of
Adolescent and School Health, National
Center for HIV/AIDS, Viral Hepatitis,
STD, and TB Prevention (NCHHSTP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) requests approval for
a new generic information collection
package that supports collection of
quantitative and qualitative information
from adults who help implement
programs and services designed to
prevent HIV, other sexually transmitted
diseases (STDs), and pregnancy or
influence related risk and protective
factors; data will be collected for needs
E:\FR\FM\04NON1.SGM
04NON1
70165
Federal Register / Vol. 85, No. 214 / Wednesday, November 4, 2020 / Notices
assessment and program refinement.
The National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention
(NCHHSTP) conducts the assessment of
program practices and health services to
reduce sexual risk behaviors among
adolescents and reduce adverse health
outcomes of those risk behaviors.
NCHHSTP conducts behavioral and
health service assessments and research
projects as part of its response to the
domestic HIV/AIDS epidemic, STD
prevention, TB elimination and viral
hepatitis control with national, state,
and local partners. Adolescents are a
population with specific developmental,
health and social, and resource needs.
Their health risk factors and access to
health care is addressed as a primary
mission by the Division of Adolescent
and School Health (DASH), and
adolescents are a population of interest
for several other NCHHSTP divisions.
The assessment and research conducted
by NCHHSTP is one pillar upon which
recommendations and guidelines are
revised and updated. Recommendations
and guidelines for adolescent sexual
risk reduction require a foundation of
scientific evidence. Assessment of
programmatic practices for adolescents
helps improve programs through better
identification of strategies relevant to
adolescents as a population as well as
specific sub-groups of adolescents at
highest risk for HIV and other STDs so
that programs can be better tailored
specifically for them.
Participants in data collection include
adults (over 18 years old) who help
implement or oversee programs to
prevent HIV, other sexually transmitted
diseases (STDs), and pregnancy among
youth or influence related risk and
protective factors. These participants
may include adults in roles such as:
• School staff and administrators
• Staff in state and local education
agencies
• Staff in state and local health agencies
• Staff in youth-serving community and
national non-governmental
organizations
• Community-based health care
providers for adolescents
• School-based health care providers for
students
The types of information collection
activities included in this generic
package are:
(1) Quantitative data collection
conducted in-person on remotely
through electronic (via computers,
tablets, other mobile devices, etc.),
telephone, or paper questionnaires to
gather information about programmatic
and service activities related to sexual
risk reduction or related adverse health
outcomes among youth. Questions relate
to work-related experiences, training,
context, duties, activities, and youths’
health and service needs. Information
may also be gathered on program
implementers’ demographic and social
characteristics, program-related
knowledge, attitudes, skills, and
implementation practices.
(2) Qualitative data collection inperson or remotely through electronic,
telephone, or paper means to gather
information about program and service
activities related to sexual risk
reduction or prevention of related
adverse health outcomes among youth.
Qualitative data collection may involve
focus groups and/or in-depth individual
or group interviews. Interview and focus
group guides may include questions
about work-related experiences,
training, context, duties, activities, and
youths’ health and service needs.
Information may also be gathered on
program implementers’ demographic
and social characteristics, programrelated knowledge, attitudes, skills, and
implementation practices. For
adolescents, data collection instruments
will include questions on demographic
characteristics; experiences with
programs and services to reduce the risk
of HIV and other STD transmission; and
knowledge, attitudes, behaviors, and
skills related to sexual risk and
protective factors on the individual,
interpersonal, and community levels.
The participants for this data
collection are considered to be the
‘‘implementers’’ of the types of
programs that are funded by CDC/
DASH. Typically, CDC/DASH programs
are intended to have direct impact on
proximal indicators such as sexual
health-related knowledge, attitudes,
perceptions, and behaviors among
youth, and although CDC/DASH
programs are typically set in schools,
they can be implemented by adults who
work in a variety of school, community,
and health-care roles.
Any data collection request put
forward under this generic clearance
will identify the programs and/or
services to be informed or refined with
the information from the collection and
will include a cross-walk of data
elements to the aspects of the program
the project team seeks to inform or
refine. Because this request includes a
wide range of possible data collection
instruments, specific requests will
include items of information to be
collected and copies of data collection
instruments. It is expected that all data
collection instruments will be pilottested, and will be culturally
appropriate for the intended
populations. All data collection
procedures will receive review and
approval by an Institutional Review
Board for the Protection of Human
Subjects and follow appropriate consent
and assent procedures as outlined in the
IRB-approved protocols, and these will
be described in the individual
information collection requests put
forward under this generic package.
Participation of respondents is
voluntary. There is no cost to the
participants other than their time.
The table below provides the
estimated annualized response burden
for up to 10 individual data collections
per year under this generic clearance.
Average burden per response is based
on pilot testing and timing of
quantitative and qualitative instrument
administration during previous studies.
Response times include the time to read
and respond to consent forms and to
read or listen to instructions. The
proposed information collections
combine for a total estimated
annualized burden of up to 60,000
hours for respondents.
khammond on DSKJM1Z7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Type of respondents
Form name
Adults helping with program implementation
(e.g., school or district staff, community
partners, NGO staff).
Adults helping with program implementation ..
Adults helping with program implementation ..
Adults helping with program implementation ..
Questionnaire .................................................
15,000
1
1
Pre/Post Questionnaire ..................................
Interview/focus group guide ...........................
Pre/Post Interview/focus group guide ............
15,000
4,000
3,000
2
1
2
1
1.5
1.5
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18:16 Nov 03, 2020
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04NON1
70166
Federal Register / Vol. 85, No. 214 / Wednesday, November 4, 2020 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–24475 Filed 11–3–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10744]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
SUMMARY:
Comments on the collection(s) of
information must be received by the
OMB desk officer by December 4, 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.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
khammond on DSKJM1Z7X2PROD with NOTICES
DATES:
VerDate Sep<11>2014
18:16 Nov 03, 2020
Jkt 253001
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
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. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Medicare
Durable Medical Equipment,
Prosthetics, Orthotics, and Supplies
(DMEPOS) Competitive Bidding
Program—Contracting Forms; Use: The
Medicare Durable Medical Equipment,
Prosthetics, Orthotics, and Supplies
(DMEPOS) Competitive Bidding
Program was established by the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (‘‘Medicare Modernization Act’’ or
‘‘MMA’’). Section 302 of the MMA
amended Section 1847 of the Social
Security Act (the Act) to establish the
competitive acquisition program and
define program requirements.
Under the MMA, the DMEPOS
Competitive Bidding Program was to be
phased in so that competition under the
program would first occur in 10 areas in
2007. The Centers for Medicare &
Medicaid Services (CMS) completed the
rulemaking process for the competitive
acquisition of DMEPOS items and
services in 42 CFR parts 411 and 414
published in the Federal Register
Volume 72 on April 10, 2007. CMS
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
conducted the Round 1 competition in
10 areas and for 10 DMEPOS product
categories, and implemented the
program on July 1, 2008. The Medicare
Improvements for Patients and
Providers Act of 2008 (MIPPA), enacted
on July 15, 2008, made limited changes
to the Competitive Bidding Program,
including termination of existing
contracts that were in effect and a
requirement to re-bid Round 1.
As required by MIPPA, CMS
conducted the competition for the
Round 1 Rebid in 2009. The Round 1
Rebid contracts and prices became
effective on January 1, 2011. The
Affordable Care Act (ACA), enacted on
March 23, 2010, expanded the Round 2
competition by adding an additional 21
metropolitan statistical areas (MSAs),
bringing the total MSAs for Round 2 to
91. The competition for Round 2 began
in December 2011. CMS also began a
competition for National Mail Order
(NMO) of diabetes testing supplies at
the same time as Round 2. The Round
2 and NMO contracts and prices were
implemented on July 1, 2013.
The MMA requires the Secretary to
recompete contracts not less often than
once every three years. The Round 1
Rebid contract period for all product
categories except mail-order diabetes
testing supplies expired on December
31, 2013. (Round 1 Rebid contracts for
mail-order diabetes testing supplies
ended on December 31, 2012.) The
competition for the Round 1 Recompete
began in August of 2012 and contracts
and prices became effective on January
1, 2014. The Round 1 Recompete
contract period expires on December 31,
2016. Round 1 2017 contracts will
become effective on January 1, 2017
through December 31, 2018. Round 2
and NMO contracts and prices expired
on June 30, 2016. Round 2 Recompete
and the NMO Recompete contracts
became effective on July 1, 2016, and
expired on December 31, 2018. CMS
will be implementing a consolidated
round of competition to include all
Round 1 2017 and Round 2 Recompete
competitive bidding areas, referred to as
Round 2021. Round 2021 will not
include NMO, which will be competed
again in future rounds of the program.
The forms included in this ICR were
previously included in the ICR currently
approved under 0938–1016. Due to the
temporary gap in the DMEPOS
Competitive Bidding Program, which
started on January 1, 2019, we do not
currently have any active PRA package
for this specific collection of
information (Form C, Subcontracting,
Change of Ownerships, and
Grandfathering). We are now seeking
approval of a PRA package based on
E:\FR\FM\04NON1.SGM
04NON1
]]>Agencies
[Federal Register Volume 85, Number 214 (Wednesday, November 4, 2020)]
[Notices]
[Pages 70164-70166]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-24475]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-21-20OG]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled ``Assessments of adults' professional
experiences for improving programs to decrease sexual risk and related
behaviors and adverse health outcomes among youth,'' to the Office of
Management and Budget (OMB) for review and approval. CDC previously
published a ``Proposed Data Collection Submitted for Public Comment and
Recommendations'' notice on June 2, 2020 to obtain comments from the
public and affected agencies. CDC did not receive comments related to
the previous notice. This notice serves to allow an additional 30 days
for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) 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;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) 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; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570. 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. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Assessments of adults' professional experiences for improving
programs to decrease sexual risk and related behaviors and adverse
health outcomes among youth--New--Division of Adolescent and School
Health, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) requests
approval for a new generic information collection package that supports
collection of quantitative and qualitative information from adults who
help implement programs and services designed to prevent HIV, other
sexually transmitted diseases (STDs), and pregnancy or influence
related risk and protective factors; data will be collected for needs
[[Page 70165]]
assessment and program refinement. The National Center for HIV/AIDS,
Viral Hepatitis, STD, and TB Prevention (NCHHSTP) conducts the
assessment of program practices and health services to reduce sexual
risk behaviors among adolescents and reduce adverse health outcomes of
those risk behaviors.
NCHHSTP conducts behavioral and health service assessments and
research projects as part of its response to the domestic HIV/AIDS
epidemic, STD prevention, TB elimination and viral hepatitis control
with national, state, and local partners. Adolescents are a population
with specific developmental, health and social, and resource needs.
Their health risk factors and access to health care is addressed as a
primary mission by the Division of Adolescent and School Health (DASH),
and adolescents are a population of interest for several other NCHHSTP
divisions. The assessment and research conducted by NCHHSTP is one
pillar upon which recommendations and guidelines are revised and
updated. Recommendations and guidelines for adolescent sexual risk
reduction require a foundation of scientific evidence. Assessment of
programmatic practices for adolescents helps improve programs through
better identification of strategies relevant to adolescents as a
population as well as specific sub-groups of adolescents at highest
risk for HIV and other STDs so that programs can be better tailored
specifically for them.
Participants in data collection include adults (over 18 years old)
who help implement or oversee programs to prevent HIV, other sexually
transmitted diseases (STDs), and pregnancy among youth or influence
related risk and protective factors. These participants may include
adults in roles such as:
School staff and administrators
Staff in state and local education agencies
Staff in state and local health agencies
Staff in youth-serving community and national non-governmental
organizations
Community-based health care providers for adolescents
School-based health care providers for students
The types of information collection activities included in this
generic package are:
(1) Quantitative data collection conducted in-person on remotely
through electronic (via computers, tablets, other mobile devices,
etc.), telephone, or paper questionnaires to gather information about
programmatic and service activities related to sexual risk reduction or
related adverse health outcomes among youth. Questions relate to work-
related experiences, training, context, duties, activities, and youths'
health and service needs. Information may also be gathered on program
implementers' demographic and social characteristics, program-related
knowledge, attitudes, skills, and implementation practices.
(2) Qualitative data collection in-person or remotely through
electronic, telephone, or paper means to gather information about
program and service activities related to sexual risk reduction or
prevention of related adverse health outcomes among youth. Qualitative
data collection may involve focus groups and/or in-depth individual or
group interviews. Interview and focus group guides may include
questions about work-related experiences, training, context, duties,
activities, and youths' health and service needs. Information may also
be gathered on program implementers' demographic and social
characteristics, program-related knowledge, attitudes, skills, and
implementation practices. For adolescents, data collection instruments
will include questions on demographic characteristics; experiences with
programs and services to reduce the risk of HIV and other STD
transmission; and knowledge, attitudes, behaviors, and skills related
to sexual risk and protective factors on the individual, interpersonal,
and community levels.
The participants for this data collection are considered to be the
``implementers'' of the types of programs that are funded by CDC/DASH.
Typically, CDC/DASH programs are intended to have direct impact on
proximal indicators such as sexual health-related knowledge, attitudes,
perceptions, and behaviors among youth, and although CDC/DASH programs
are typically set in schools, they can be implemented by adults who
work in a variety of school, community, and health-care roles.
Any data collection request put forward under this generic
clearance will identify the programs and/or services to be informed or
refined with the information from the collection and will include a
cross-walk of data elements to the aspects of the program the project
team seeks to inform or refine. Because this request includes a wide
range of possible data collection instruments, specific requests will
include items of information to be collected and copies of data
collection instruments. It is expected that all data collection
instruments will be pilot-tested, and will be culturally appropriate
for the intended populations. All data collection procedures will
receive review and approval by an Institutional Review Board for the
Protection of Human Subjects and follow appropriate consent and assent
procedures as outlined in the IRB-approved protocols, and these will be
described in the individual information collection requests put forward
under this generic package. Participation of respondents is voluntary.
There is no cost to the participants other than their time.
The table below provides the estimated annualized response burden
for up to 10 individual data collections per year under this generic
clearance. Average burden per response is based on pilot testing and
timing of quantitative and qualitative instrument administration during
previous studies. Response times include the time to read and respond
to consent forms and to read or listen to instructions. The proposed
information collections combine for a total estimated annualized burden
of up to 60,000 hours for respondents.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Adults helping with program Questionnaire........... 15,000 1 1
implementation (e.g., school or
district staff, community partners,
NGO staff).
Adults helping with program Pre/Post Questionnaire.. 15,000 2 1
implementation.
Adults helping with program Interview/focus group 4,000 1 1.5
implementation. guide.
Adults helping with program Pre/Post Interview/focus 3,000 2 1.5
implementation. group guide.
----------------------------------------------------------------------------------------------------------------
[[Page 70166]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-24475 Filed 11-3-20; 8:45 am]
BILLING CODE 4163-18-P
