Proposed Data Collection Submitted for Public Comment and Recommendations, 86901-86903 [2023-27550]
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Federal Register / Vol. 88, No. 240 / Friday, December 15, 2023 / Notices
Requested Information From Industry
To help GSA assess the ability of
nonprofit computer refurbishers or other
industry partners to participate in the
COVS Act program, please answer the
following questions:
General
• If you are a nonprofit computer
refurbisher, what is the name, mission,
vision, location, and history of your
nonprofit organization? How long have
you been operating as a nonprofit
computer refurbisher or industry
partner?
• What are your sources of funding
and support? How do you ensure
financial sustainability and
accountability?
• How many staff members and
volunteers do you have? What are their
roles and qualifications? How do you
recruit, train, and retain them?
ddrumheller on DSK120RN23PROD with NOTICES1
Refurbishing
• How many computers and
technology equipment do you refurbish
per year? What are the types, models,
brands, and specifications of the
equipment you refurbish? What are the
standards and procedures you follow for
refurbishing?
• When do you consider computer or
technology equipment obsolete or
unrepairable? Is there any type of
surplus computer or technology
equipment that you will not accept? For
example, computers without hard drives
or equipment over a certain age.
• Do you provide data sanitization
services? Do you follow the National
Institute of Standards and Technology
(NIST Special Publication 800–88, Rev.
1) guidelines? Do you provide evidence/
reports that sanitization was completed?
Recycling
• If computer or technology
equipment cannot be repaired or reused,
what do you do with the property? Are
you a certified electronics recycler? If
so, under which standard? If not, do you
partner with certified electronics
recyclers?
• How many computers and
technology equipment do you recycle
per year? What are the types, models,
brands, and specifications of the
equipment you recycle? What are the
standards and procedures you follow for
recycling?
Distribution
• What process would you use to
identify recipients eligible to receive
surplus computer or technology
equipment in accordance with 40 U.S.C.
549a? How would you verify eligibility
to prevent ineligible persons from
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17:57 Dec 14, 2023
Jkt 262001
obtaining equipment? How would you
determine who receives the equipment
to ensure fair and equitable
distribution?
• Would recipients be required to pay
for the equipment? How would you
determine the price or fee in compliance
with 40 U.S.C. 549a(b)(3)(B)?
• Is your organization able to
segregate equipment received under the
COVS Act from other sources to ensure
this equipment is only provided to
eligible recipients?
• Federal agencies are generally
unable to pay for shipping and
transportation to refurbishers. Would
you cover shipping costs? Would you be
able to pick up computers and
equipment from agency locations?
• How would you distribute
refurbished computers and technology
equipment to recipients? What would be
your distribution network and criteria?
How would you ensure quality control
and customer service?
• How long (in days) would it take to
refurbish computers (from the date the
equipment is received) and provide
them to eligible recipients?
Training
• Do you offer training programs on
the use of the repaired computers and
technology equipment? Is this training
provided at no cost, or for a fee? If there
is a charge for the classes, how is this
fee determined?
• Please describe the training
programs, platforms (e.g., in person,
virtual) and the target audiences.
Reporting
• Nonprofit computer refurbishers
receiving surplus computer or
technology equipment under the COVS
Act are required to report information to
GSA on a recurring basis. This includes
information about the distribution of the
equipment and which eligible recipients
received the equipment. Would you be
able to provide the required recipient
data and reports to GSA? How soon
could you provide reports about who
received the equipment (taking into
account the time to repair and transfer
them)? Do you foresee any challenges in
providing this data to GSA?
Partnerships
• Do you have any experience
working with Federal agencies or
receiving surplus computers and
technology equipment from them? If so,
please provide examples.
• How do you envision
nongovernmental entities partnering
with GSA? Do you anticipate any
challenges with GSA establishing
partnerships with nongovernmental
PO 00000
Frm 00029
Fmt 4703
Sfmt 4703
86901
entities to facilitate the identification
and participation of nonprofit computer
refurbishers?
• Are you aware of any nonprofit
computer refurbisher groups, alliances,
or associations? If yes, please list them.
Are there other types of groups we need
to be aware of in the industry?
• Are you a member of a nonprofit
computer refurbisher group, alliance, or
association? If yes, which one? What are
the eligibility and certification
requirements to join? Are you required
to pay any fees to participate? Why did
you decide to join one or choose one
particular group, alliance, or association
over another?
• If you’re not part of a group,
alliance, or association, is there a reason
you have not joined or are you opposed
to joining one?
Other
• Please provide any additional
comments or challenges you anticipate
related to participating in the COVS Act
program.
Krystal J. Brumfield,
Associate Administrator, Office of
Government-wide Policy, U.S. General
Services Administration.
[FR Doc. 2023–27536 Filed 12–14–23; 8:45 am]
BILLING CODE 6820–14–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–0909; Docket No. CDC–2023–
0096]
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 to comment on a continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on the
proposed data collection titled, CDC
Diabetes Prevention Recognition
Program (DPRP). The Diabetes
Prevention Recognition Program (DPRP)
continues the collection of nationwide,
de-identified data for the
SUMMARY:
E:\FR\FM\15DEN1.SGM
15DEN1
ddrumheller on DSK120RN23PROD with NOTICES1
86902
Federal Register / Vol. 88, No. 240 / Friday, December 15, 2023 / Notices
implementation of the National Diabetes
Prevention Program (National DPP)
lifestyle change program using a set of
evidence-based standards.
DATES: CDC must receive written
comments on or before February 13,
2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0096 by either of the following methods:
• Federal eRulemaking Portal:
www.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
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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
H21–8, Atlanta, Georgia 30329;
Telephone: 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
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
VerDate Sep<11>2014
17:57 Dec 14, 2023
Jkt 262001
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
CDC Diabetes Prevention Recognition
Program (DPRP)—Revision—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC’s Division of Diabetes
Translation (DDT) established and
administers the National Diabetes
Prevention Recognition Program
(DPRP), which recognizes organizations
that deliver a diabetes prevention
program according to evidence-based
requirements set forth in the CDC’s
Diabetes Prevention Recognition
Program Standards and Operating
Procedures (DPRP Standards).
Additionally, the Centers for Medicare &
Medicaid Services (CMS) Medicare
Diabetes Prevention Program (MDPP)
expansion of CDC’s National DPP was
announced in early 2016, when the
Secretary of Health and Human Services
(HHS) determined that the Diabetes
Prevention Program met the statutory
criteria for inclusion in Medicare’s
expanded list of health care services for
beneficiaries (https://cmmi.my.site.com/
mdpp/). This was the first time a
preventive service model from the CMS
Innovation Center was expanded into
Medicare. After extensive testing of this
model in 17 sites across the US from
2014–2016, CMS proposed the MDPP in
Sections 1102 and 1871 of the Social
Security Act (42 U.S.C. 1302 and
1395hh section 424.59), authorizing
CDC-recognized organizations to
prepare for enrollment as MDPP
suppliers beginning in January 2018 in
order to bill CMS for these services.
Only organizations in good standing
with the CDC DPRP are eligible as
MDPP suppliers. CDC continues to work
with CMS to support the MDPP.
CDC requests an additional three
years of OMB approval to continue
collecting the information needed to
administer the DPRP and provide
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
information needed by CMS to support
the MDPP benefit. Based on experience
with the DPRP from 2011–2023,
including data analysis and feedback
from applicant organizations and
internal and external partners, CDC
plans to revise the DPRP Standards and
the associated information collection.
Key changes are a direct result of DPRP
data analyses, recent literature reviews,
and discussion with National DPP
stakeholders, including those serving
socially vulnerable populations. Key
changes to the evaluation data
collection instrument allow for the
collection of participant zip codes (for
aggregate reporting only, not to be
reported per each individual
participant); an OMB-recommended 6point disability variable; a health
equity-related social determinants of
health (SDOH) variable set (to assess
whether there was a social needs
assessment conducted; key SDOH issues
identified; and whether any action was
taken); a Middle Eastern or North
African write-in option within the
current race/ethnicity variable; and two
new options for the current payersource
variable.
Key changes to the application data
collection instrument allow for: (1) a
yes/no drop-down question asking if an
organization’s zip code is in an area of
high social vulnerability based on the
Social Vulnerability Index, which
would permit an in-person organization
to be fast-tracked to preliminary
recognition status to allow the
organization to apply to CMS to become
an MDPP supplier; (2) revisions to the
Combination delivery mode to include
an option for in-person delivery with a
distance learning component; and (3)
collection of a projected program startdate.
During the period of this Revision,
CDC estimates receipt of approximately
200 DPRP application forms per year
from new organizations. The estimated
burden per one-time application
response is one hour. In addition, CDC
estimates receipt of semi-annual
evaluation data submissions from the
same 200 additional organizations per
year, estimated at two hours per
response. The total estimated average
annualized evaluation burden to new
respondents is 2,400 hours. This
includes an estimate of the time needed
to extract and compile the required data
records and fields from an existing
electronic database, review the data, and
enter the data via the DPRP Data Portal.
CDC also has 1,500 currently recognized
organizations that will continue to
submit semi-annual evaluation data.
The estimated burden per response is
modest, since the information requested
E:\FR\FM\15DEN1.SGM
15DEN1
86903
Federal Register / Vol. 88, No. 240 / Friday, December 15, 2023 / Notices
for DPRP recognition is routinely
collected by most organizations that
deliver the National DPP lifestyle
change program for their own internal
evaluation and possible insurance
reimbursement purposes, including the
MDPP benefit. Participation in the DPRP
is voluntary, data are de-identified, no
personally identifiable information (PII)
is collected by CDC, and there are no
costs to respondents other than their
time. CDC is requesting a three-year
revised approval. The total estimated
annual burden hours requested is 7,400.
ESTIMATED ANNUALIZED BURDEN HOURS FOR NEW ORGANIZATIONS
Number of
respondents
Number of
responses per
respondent
Application Form ...........
Evaluation Data ............
Application Form ...........
Evaluation Data ............
80
680
120
1,120
1
2
1
2
1
2
1
2
80
2,720
120
4,480
..................................................
....................
........................
........................
7,400
Type of respondent
Form name
Public sector organizations that deliver the National DPP lifestyle change program.
Private sector organizations that deliver the
National DPP lifestyle change program.
Total ............................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2023–27550 Filed 12–14–23; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–1186; Docket No. CDC–2023–
0099]
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 continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Information
Collection for Tuberculosis Data from
Referring Entities to CureTB. The
CureTB program works to prevent the
spread of tuberculosis (TB) among
people who cross international borders
by providing linkage to care for patients
with active/suspected TB when they
leave the U.S., accurate and up-to-date
information for receiving providers,
motivation and resources for mobile
individuals to continue care, linkage for
comorbidities, and facilitation of
ddrumheller on DSK120RN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:57 Dec 14, 2023
Jkt 262001
DPRP
DPRP
DPRP
DPRP
positive outcomes and communication
between partners.
DATES: CDC must receive written
comments on or before February 13,
2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0099 by either of the following methods:
• Federal eRulemaking Portal:
www.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
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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
H21–8, Atlanta, Georgia 30329;
Telephone: 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
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
Avg. burden
per response
(in hours)
Total burden
(in hours)
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
Information Collection for
Tuberculosis Data from Referring
Entities to CureTB (OMB Control No.
0920–1186, Exp. 2/29/2024)—
Extension—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The CureTB program at CDC works to
prevent the spread of tuberculosis (TB)
among people who cross international
borders. To reduce disease transmission
and the emergence of drug-resistant TB,
E:\FR\FM\15DEN1.SGM
15DEN1
]]>Agencies
[Federal Register Volume 88, Number 240 (Friday, December 15, 2023)]
[Notices]
[Pages 86901-86903]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-27550]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-0909; Docket No. CDC-2023-0096]
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 to comment on a continuing information collection, as
required by the Paperwork Reduction Act of 1995. This notice invites
comment on the proposed data collection titled, CDC Diabetes Prevention
Recognition Program (DPRP). The Diabetes Prevention Recognition Program
(DPRP) continues the collection of nationwide, de-identified data for
the
[[Page 86902]]
implementation of the National Diabetes Prevention Program (National
DPP) lifestyle change program using a set of evidence-based standards.
DATES: CDC must receive written comments on or before February 13,
2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2023-
0096 by either of the following methods:
Federal eRulemaking Portal: www.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 www.regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (www.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 H21-8, Atlanta, Georgia 30329; Telephone: 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
CDC Diabetes Prevention Recognition Program (DPRP)--Revision--
National Center for Chronic Disease Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
CDC's Division of Diabetes Translation (DDT) established and
administers the National Diabetes Prevention Recognition Program
(DPRP), which recognizes organizations that deliver a diabetes
prevention program according to evidence-based requirements set forth
in the CDC's Diabetes Prevention Recognition Program Standards and
Operating Procedures (DPRP Standards). Additionally, the Centers for
Medicare & Medicaid Services (CMS) Medicare Diabetes Prevention Program
(MDPP) expansion of CDC's National DPP was announced in early 2016,
when the Secretary of Health and Human Services (HHS) determined that
the Diabetes Prevention Program met the statutory criteria for
inclusion in Medicare's expanded list of health care services for
beneficiaries (https://cmmi.my.site.com/mdpp/). This was the first time
a preventive service model from the CMS Innovation Center was expanded
into Medicare. After extensive testing of this model in 17 sites across
the US from 2014-2016, CMS proposed the MDPP in Sections 1102 and 1871
of the Social Security Act (42 U.S.C. 1302 and 1395hh section 424.59),
authorizing CDC-recognized organizations to prepare for enrollment as
MDPP suppliers beginning in January 2018 in order to bill CMS for these
services. Only organizations in good standing with the CDC DPRP are
eligible as MDPP suppliers. CDC continues to work with CMS to support
the MDPP.
CDC requests an additional three years of OMB approval to continue
collecting the information needed to administer the DPRP and provide
information needed by CMS to support the MDPP benefit. Based on
experience with the DPRP from 2011-2023, including data analysis and
feedback from applicant organizations and internal and external
partners, CDC plans to revise the DPRP Standards and the associated
information collection. Key changes are a direct result of DPRP data
analyses, recent literature reviews, and discussion with National DPP
stakeholders, including those serving socially vulnerable populations.
Key changes to the evaluation data collection instrument allow for the
collection of participant zip codes (for aggregate reporting only, not
to be reported per each individual participant); an OMB-recommended 6-
point disability variable; a health equity-related social determinants
of health (SDOH) variable set (to assess whether there was a social
needs assessment conducted; key SDOH issues identified; and whether any
action was taken); a Middle Eastern or North African write-in option
within the current race/ethnicity variable; and two new options for the
current payersource variable.
Key changes to the application data collection instrument allow
for: (1) a yes/no drop-down question asking if an organization's zip
code is in an area of high social vulnerability based on the Social
Vulnerability Index, which would permit an in-person organization to be
fast-tracked to preliminary recognition status to allow the
organization to apply to CMS to become an MDPP supplier; (2) revisions
to the Combination delivery mode to include an option for in-person
delivery with a distance learning component; and (3) collection of a
projected program start-date.
During the period of this Revision, CDC estimates receipt of
approximately 200 DPRP application forms per year from new
organizations. The estimated burden per one-time application response
is one hour. In addition, CDC estimates receipt of semi-annual
evaluation data submissions from the same 200 additional organizations
per year, estimated at two hours per response. The total estimated
average annualized evaluation burden to new respondents is 2,400 hours.
This includes an estimate of the time needed to extract and compile the
required data records and fields from an existing electronic database,
review the data, and enter the data via the DPRP Data Portal. CDC also
has 1,500 currently recognized organizations that will continue to
submit semi-annual evaluation data. The estimated burden per response
is modest, since the information requested
[[Page 86903]]
for DPRP recognition is routinely collected by most organizations that
deliver the National DPP lifestyle change program for their own
internal evaluation and possible insurance reimbursement purposes,
including the MDPP benefit. Participation in the DPRP is voluntary,
data are de-identified, no personally identifiable information (PII) is
collected by CDC, and there are no costs to respondents other than
their time. CDC is requesting a three-year revised approval. The total
estimated annual burden hours requested is 7,400.
Estimated Annualized Burden Hours for New Organizations
----------------------------------------------------------------------------------------------------------------
Number of Avg. burden Total
Type of respondent Form name Number of responses per per response burden (in
respondents respondent (in hours) hours)
----------------------------------------------------------------------------------------------------------------
Public sector organizations that DPRP Application 80 1 1 80
deliver the National DPP Form. 680 2 2 2,720
lifestyle change program. DPRP Evaluation
Data.
Private sector organizations that DPRP Application 120 1 1 120
deliver the National DPP Form. 1,120 2 2 4,480
lifestyle change program. DPRP Evaluation
Data.
------------------------------------------------------------------------------
Total........................ ................... ........... .............. .............. 7,400
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health
Ethics and Regulations, Office of Science, Centers for Disease Control
and Prevention.
[FR Doc. 2023-27550 Filed 12-14-23; 8:45 am]
BILLING CODE 4163-18-P
