Proposed Data Collection Submitted for Public Comment and Recommendations
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Abstract
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 Evaluation of the Division of Overdose Prevention Technical Assistance Center. This data collection activity is focused on comprehensive and interdisciplinary opioid overdose prevention efforts in 90 jurisdictions.
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<title>Federal Register, Volume 91 Issue 216 (Tuesday, November 10, 2026)</title>
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[Federal Register Volume 91, Number 216 (Tuesday, November 10, 2026)]
[Notices]
[Pages 72540-72541]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-22881]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-27-1355; Docket No. CDC-2026-1751]
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.
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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 continuing information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed information collection project
titled Evaluation of the Division of Overdose Prevention Technical
Assistance Center. This data collection activity is focused on
comprehensive and interdisciplinary opioid overdose prevention efforts
in 90 jurisdictions.
DATES: CDC must receive written comments on or before January 11, 2027.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2026-
1751 by either of the following methods:
<bullet> Federal eRulemaking Portal: <a href="http://www.regulations.gov">www.regulations.gov</a>. Follow
the instructions for submitting comments.
<bullet> 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 <a href="http://www.regulations.gov">www.regulations.gov</a>.
Please note: Submit all comments through the Federal eRulemaking
portal (<a href="http://www.regulations.gov">www.regulations.gov</a>) 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: <a href="/cdn-cgi/l/email-protection#c7a8aaa587a4a3a4e9a0a8b1"><span class="__cf_email__" data-cfemail="016e6c63416265622f666e77">[email protected]</span></a>.
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
Evaluation of the Division of Overdose Prevention Technical
Assistance Center (OMB Control No. 0920-1355, Exp. 12/31/2027)--
Extension--National Center for Injury Prevention and Control (NCIPC),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
This Extension is being submitted to support the evaluation of
technical assistance (TA) provided for the Overdose Data to Action
(OD2A) in States (S) and OD2A: Limiting Overdose through Collaborative
Actions in Localities (LOCAL) programs. OD2A-S and OD2A: LOCAL are
cooperative agreements funded in 2023 to focus on comprehensive and
interdisciplinary opioid overdose prevention efforts in 90
[[Page 72541]]
jurisdictions, including 49 state health departments, 39 localities,
Puerto Rico, and Washington DC. Each program consists of two required
components; a surveillance component and a prevention component. OD2A
recipients implement a combination of activities across nine state
strategies and eight local strategies within these components to gain
access to high quality, complete, and timelier data on opioid
prescribing and overdoses, and to use those data to inform prevention
and response efforts in their jurisdictions.
In the previously approved iteration of this information collection
request (ICR), the information collected surrounding OD2A recipient
feedback on their experiences receiving TA has been invaluable in
improving TA delivery. The feedback provided in the original data
collection instruments was also used to improve the TA Strategy of OD2A
at large. Further information gathering will enhance TA perspectives
and needs to utilize the Division of Overdose Prevention (DOP) TA
Center resource effectively and responsibly.
Training and TA is essential to building knowledge and
strengthening the capacity of recipients to implement and evaluate OD2A
program strategies. CDC developed and deployed a TA hub (hereafter
referred to as the DOP TA Center) to deliver comprehensive technical
assistance and training to support the successful implementation and
evaluation of surveillance and prevention activities. The DOP TA Center
is designed to enhance the efficiency, coordination, and effectiveness
of TA efforts by streamlining and centralizing the provision of
overdose surveillance and prevention TA. TA to OD2A recipients is
divided into four different levels with multiple modes of TA delivery
and involves a wide range of TA providers including CDC staff, internal
and external subject matter experts (SMEs) and program partners as well
as Tanaq and ICF staff. The TA levels are used to direct the process
for engaging stakeholders to support program recipients and triage
appropriate resources to support their needs.
This package aims to extend approval for the instruments previously
approved. CDC requests OMB approval for an estimated 388 annual burden
hours. There are no costs to respondents other than their time to
participate.
Estimated Annualized Burden Hours
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Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
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OD2A (OD2A in States and OD2A: LOCAL) TA Feedback Form Individual............ 618 2 5/60 103
Recipients.
TA Feedback Form Universal............. 617 2 5/60 103
Annual Technical Assistance Survey..... 162 1 10/60 27
Implementation Feedback Survey......... 18 1 15/60 5
Email invitation for Annual Survey..... 900 1 2/60 30
Focus Groups Email invitation.......... 600 1 2/60 20
Focus Group Session.................... 100 1 1 100
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Total...................................... ....................................... .............. .............. .............. 388
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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. 2026-22881 Filed 11-9-26; 8:45 am]
BILLING CODE 4163-18-P
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