Agency Forms Undergoing Paperwork Reduction Act Review, 30940-30941 [2021-12208]
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30940
Federal Register / Vol. 86, No. 110 / Thursday, June 10, 2021 / Notices
(4) Inform continuous quality
improvement activities over the course
of the funding period, to include
quarterly and annual strategic planning
for current and later iterations of this
program under future funding.
CDC requests OMB approval for an
estimated 655 annual burden hours.
There are no costs to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Total burden
(in hours)
Form name
Core SIPP Program Awardees .........
Implementation Capacity Development Rubric.
Economic Indicators .........................
Recipient-level Group Interviews .....
Injury Indicators Spreadsheet ..........
Emergency Department Injury Indicators Spreadsheet.
Hospital Discharge Injury Indicators
Spreadsheet.
Special Emphasis Reports ...............
23
1
2
46
23
23
23
23
1
1
1
1
1
1.5
5
5
23
35
107
107
23
1
5
107
23
1
10
230
...........................................................
........................
........................
........................
655
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–12211 Filed 6–9–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–21–21BL]
Agency Forms Undergoing Paperwork
Reduction Act Review
khammond on DSKJM1Z7X2PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Type of respondents
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Evaluation of
the Overdose Data to Action Technical
Assistance Hub’’ 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 December
11, 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
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22:14 Jun 09, 2021
Jkt 253001
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.
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
Proposed Project
Evaluation of the Overdose Data to
Action Technical Assistance Hub—
New—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC)
Background and Brief Description
The Division of Overdose Prevention
(DOP), at Centers for Disease Control
and Prevention (CDC) requests a threeyear OMB approval to support the
evaluation of technical assistance (TA)
provided for the Overdose Data to
Action (OD2A) program. OD2A is a
cooperative agreement (CDC–RFA–
CE19–1904) funded in 2019 to focus on
comprehensive and interdisciplinary
opioid overdose prevention efforts in 47
state health departments, 16 localities,
Puerto Rico, Washington DC, and the
North Mariana Islands. This program
consists of two required components—
a surveillance component and a
prevention component. OD2A recipients
implement a combination of activities
across 10 strategies within these
components in order 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.
Training and technical assistance
(TA) is essential to building knowledge
and strengthening the capacity of
recipients to implement and evaluate
OD2A program strategies. CDC will
develop and deploy a TA hub (hereafter
referred to as the OD2A TA Center) to
deliver comprehensive technical
assistance and training to support the
successful implementation and
E:\FR\FM\10JNN1.SGM
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30941
Federal Register / Vol. 86, No. 110 / Thursday, June 10, 2021 / Notices
evaluation of surveillance and
prevention activities. The OD2A 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
contract staff.
The evaluation consists of two webbased surveys designed to collect
process and outcome measures about
TA access, utilization, and outcomes
across all 66 OD2A recipient programs.
The Technical Assistance Feedback
Form will be administered to collect
immediate feedback following
individual TA encounters and group
events such as webinars and in-person
trainings. The Annual OD2A TA Survey
will be distributed twice (mid-point and
final) to assess satisfaction with overall
TA provided and the extent to which
TA supports informed implementation
of OD2A strategies. The information
obtained through this evaluation will
allow TA providers to assess OD2A
recipients’ experience and utility of
knowledge and resources gained
through individual TA support, peer-topeer sessions, and other group trainings.
Ultimately, the evaluation data will
inform subsequent rounds of TA and
allow TA providers to make necessary
adjustments to the overall TA strategy
for continuous quality improvement.
This will ensure recipients have the
support necessary to implement
strategies that will improve opioid
surveillance and prevention policies
and practices within their communities.
The total annualized burden estimate
is 222 hours. There is no cost to
respondents other than the time to
participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
OD2A Recipients ............................................
TA Feedback Form ........................................
Annual OD2A Survey .....................................
Email invitation and reminders for OD2A
Survey.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–12208 Filed 6–9–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; National
Agriculture and Food Defense Strategy
Survey
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Submit written comments
(including recommendations) on the
collection of information by July 12,
2021.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
SUMMARY:
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17:15 Jun 09, 2021
Jkt 253001
comments be submitted to https://
www.reginfo.gov/public/do/PRAMain.
Find this particular information
collection by selecting ‘‘Currently under
Review—Open for Public Comments’’ or
by using the search function. The OMB
control number for this information
collection is 0910–0855. Also include
the FDA docket number found in
brackets in the heading of this
document.
Ila
S. Mizrachi, Office of Operations, Food
and Drug Administration, Three White
Flint North, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–7726, PRAStaff@
fda.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
[Docket No. FDA–2018–N–1129]
khammond on DSKJM1Z7X2PROD with NOTICES
Number of
respondents
Type of respondents
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
National Agriculture and Food Defense
Strategy Survey
OMB Control Number 0910–0855—
Extension
We are seeking OMB approval of the
National Agriculture and Food Defense
Strategy (NAFDS) under section 108 of
the FDA Food and Safety Modernization
Act (FSMA). This is a voluntary survey
of State, local, territorial, and/or tribal
(SLTT) governments intended to gauge
government activities in food and
agriculture defense from intentional
PO 00000
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671
440
440
Number of
responses per
respondent
2
1
1
Average
burden per
response
(in hours)
5/60
13/60
2/60
contamination and emerging threats.
The collected information will be
included in the mandatory NAFDS
followup Report to Congress. The
authority for us to collect the
information derives from the
Commissioner of Food and Drugs’
authority provided in section
1003(d)(2)(C) of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C.
393(d)(2)(C)).
Protecting the nation’s food and
agriculture supply against intentional
contamination and other emerging
threats is an important responsibility
shared by SLTT governments as well as
private sector partners. On January 4,
2011, the President signed into law
FSMA. FSMA focuses on ensuring the
safety of the U.S. food supply by
shifting the efforts of Federal regulators
from response to prevention and
recognizes the importance of
strengthening existing collaboration
among all stakeholders to achieve
common public health and security
goals. FSMA identifies some key
priorities for working with partners in
areas such as reliance on Federal, State,
and local agencies for inspections;
improving foodborne illness
surveillance; and leveraging and
enhancing State and local food safety
and defense capacities. Section 108 of
FSMA (NAFDS) requires the
Department of Health and Human
Services (HHS) and the U.S. Department
of Agriculture (USDA), in coordination
E:\FR\FM\10JNN1.SGM
10JNN1
]]>Agencies
[Federal Register Volume 86, Number 110 (Thursday, June 10, 2021)]
[Notices]
[Pages 30940-30941]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-12208]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-21-21BL]
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 ``Evaluation of the Overdose Data to Action
Technical Assistance Hub'' 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
December 11, 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
Evaluation of the Overdose Data to Action Technical Assistance Hub--
New--National Center for Injury Prevention and Control (NCIPC), Centers
for Disease Control and Prevention (CDC)
Background and Brief Description
The Division of Overdose Prevention (DOP), at Centers for Disease
Control and Prevention (CDC) requests a three-year OMB approval to
support the evaluation of technical assistance (TA) provided for the
Overdose Data to Action (OD2A) program. OD2A is a cooperative agreement
(CDC-RFA-CE19-1904) funded in 2019 to focus on comprehensive and
interdisciplinary opioid overdose prevention efforts in 47 state health
departments, 16 localities, Puerto Rico, Washington DC, and the North
Mariana Islands. This program consists of two required components--a
surveillance component and a prevention component. OD2A recipients
implement a combination of activities across 10 strategies within these
components in order 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.
Training and technical assistance (TA) is essential to building
knowledge and strengthening the capacity of recipients to implement and
evaluate OD2A program strategies. CDC will develop and deploy a TA hub
(hereafter referred to as the OD2A TA Center) to deliver comprehensive
technical assistance and training to support the successful
implementation and
[[Page 30941]]
evaluation of surveillance and prevention activities. The OD2A 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 contract staff.
The evaluation consists of two web-based surveys designed to
collect process and outcome measures about TA access, utilization, and
outcomes across all 66 OD2A recipient programs. The Technical
Assistance Feedback Form will be administered to collect immediate
feedback following individual TA encounters and group events such as
webinars and in-person trainings. The Annual OD2A TA Survey will be
distributed twice (mid-point and final) to assess satisfaction with
overall TA provided and the extent to which TA supports informed
implementation of OD2A strategies. The information obtained through
this evaluation will allow TA providers to assess OD2A recipients'
experience and utility of knowledge and resources gained through
individual TA support, peer-to-peer sessions, and other group
trainings. Ultimately, the evaluation data will inform subsequent
rounds of TA and allow TA providers to make necessary adjustments to
the overall TA strategy for continuous quality improvement. This will
ensure recipients have the support necessary to implement strategies
that will improve opioid surveillance and prevention policies and
practices within their communities.
The total annualized burden estimate is 222 hours. There is no cost
to respondents other than the time to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
OD2A Recipients....................... TA Feedback Form........ 671 2 5/60
Annual OD2A Survey...... 440 1 13/60
Email invitation and 440 1 2/60
reminders for OD2A
Survey.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-12208 Filed 6-9-21; 8:45 am]
BILLING CODE 4163-18-P
