Proposed Data Collection Submitted for Public Comment and Recommendations, 11990-11991 [2020-04082]
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11990
Federal Register / Vol. 85, No. 40 / Friday, February 28, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
..........................................................
........................
........................
........................
Type of respondents
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–04081 Filed 2–27–20; 8:45 am]
BILLING CODE 4163–18–P
Please Note: Submit all comments through
the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
FOR FURTHER INFORMATION CONTACT:
[60Day–20–20JC; Docket No. CDC–2020–
0023]
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 ‘‘Delta Impact Cooperative
Agreement Evaluation Data Collection
Instruments’’, to collect information
from recipients related to program
evaluation activities for cooperative
agreement CDC–RFA–CE18–1801:
Domestic Violence Prevention
Enhancement and Leadership Through
Alliances (DELTA) Impact.
DATES: Written comments must be
received on or before April 28, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0023 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
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:27 Feb 27, 2020
Jkt 250001
Clifton Road NE, MS–D74, 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.
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
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; and
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
Total burden
(in hours)
1,449
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.
5. Assess information collection costs.
Proposed Project
Delta impact Cooperative Agreement
Evaluation Data Collection
Instruments—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) seeks OMB approval
for three years for a new information
collection request to collect information
from all 10 recipients (State Domestic
Violence Coalitions) and all 17
subrecipients (Coordinated Community
Response teams) funded through CDC’s
Domestic Violence Prevention
Enhancements and Leadership Through
Alliances (DELTA) Impact Program
cooperative agreement (NOFO CDC–
RFA–CE18–1801). CDC will collect
information from DELTA Impact
recipients as part of its program
evaluation to assess the implementation
and impact of the NOFO and further
understand the facilitators, barriers, and
critical factors to implement specific
violence prevention strategies and
conduct program evaluation activities.
The findings from this data collection
will be used for implementing and
evaluating DELTA Impact prevention
efforts, and will inform technical
assistance provided to recipients to
assist them in achieving the goals of the
DELTA Impact program. This data
collection will supplement other data to
highlight recipient and subrecipients’
experiences implementing their primary
prevention efforts to prevent intimate
partner violence and their related
program evaluation activities. CDC
requests approval for 47 burden hours
annually. There is no cost to
respondents other than their time.
E:\FR\FM\28FEN1.SGM
28FEN1
11991
Federal Register / Vol. 85, No. 40 / Friday, February 28, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
DELTA Impact Program Recipients
State Domestic Violence Coalitions.
Total ...........................................
Key Informant
Lead (Att. 3).
1
1
10
Key Informant Interview—Evaluator
(Att. 4).
Subrecipient Survey (Att. 5) .............
Prevention Infrastructure Assessment (Att. 6).
10
1
45/60
8
17
10
1
2
30/60
1
9
20
...........................................................
........................
........................
........................
47
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–20JE; Docket No. CDC–2020–
0025]
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 ‘‘Distribution of Traceable Opioid
Material* Kits (TOM Kits*) across U.S.
Laboratories.’’ CDC will use a brief webbased survey to collect information from
laboratories submitting requests for
TOM Kits*. CDC will use this
information to prioritize which
laboratories will receive kits when
quantities are limited.
* TRACEABLE OPIOID MATERIAL,
TOM KITS, and the TOM KITS logo are
marks of the U.S. Department of Health
and Human Services.
DATES: CDC must receive written
comments on or before April 28, 2020.
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
Total burden
(in hours)
10
[FR Doc. 2020–04082 Filed 2–27–20; 8:45 am]
17:27 Feb 27, 2020
Average
burden per
response
(in hours)
Interview—Project
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
VerDate Sep<11>2014
Number of
responses per
respondent
Number of
respondent
Form name
Jkt 250001
You may submit comments,
identified by Docket No. CDC–2020–
0025 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–D74, 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.
ADDRESSES:
Please note: Submit all comments through
the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
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
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.
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
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; and
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.
5. Assess information collection costs.
Proposed Project
Distribution of Traceable Opioid
Material* Kits (TOM Kits*) across U.S.
Laboratories—NEW—National Center
for Environmental Health (NCEH),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
For the first time in U.S. history, a
drug class has been declared a national
public health emergency; each day more
than 140 Americans die from drug
overdoses, 91 specifically because of
opioids. Since 2013, there have been
significant increases in overdose deaths
involving synthetic opioids—
particularly those involving illicitlymanufactured fentanyl. The U.S. Drug
Enforcement Administration (DEA)
estimates that 75 percent of all opioid
identifications are illicit fentanyls.
Laboratories are routinely asked to
confirm which fentanyl or other opioids
E:\FR\FM\28FEN1.SGM
28FEN1
]]>Agencies
[Federal Register Volume 85, Number 40 (Friday, February 28, 2020)]
[Notices]
[Pages 11990-11991]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-04082]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-20-20JC; Docket No. CDC-2020-0023]
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 ``Delta Impact Cooperative
Agreement Evaluation Data Collection Instruments'', to collect
information from recipients related to program evaluation activities
for cooperative agreement CDC-RFA-CE18-1801: Domestic Violence
Prevention Enhancement and Leadership Through Alliances (DELTA) Impact.
DATES: Written comments must be received on or before April 28, 2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0023 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-D74, 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; and
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.
5. Assess information collection costs.
Proposed Project
Delta impact Cooperative Agreement Evaluation Data Collection
Instruments--New--National Center for Injury Prevention and Control
(NCIPC), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) seeks OMB
approval for three years for a new information collection request to
collect information from all 10 recipients (State Domestic Violence
Coalitions) and all 17 subrecipients (Coordinated Community Response
teams) funded through CDC's Domestic Violence Prevention Enhancements
and Leadership Through Alliances (DELTA) Impact Program cooperative
agreement (NOFO CDC-RFA-CE18-1801). CDC will collect information from
DELTA Impact recipients as part of its program evaluation to assess the
implementation and impact of the NOFO and further understand the
facilitators, barriers, and critical factors to implement specific
violence prevention strategies and conduct program evaluation
activities.
The findings from this data collection will be used for
implementing and evaluating DELTA Impact prevention efforts, and will
inform technical assistance provided to recipients to assist them in
achieving the goals of the DELTA Impact program. This data collection
will supplement other data to highlight recipient and subrecipients'
experiences implementing their primary prevention efforts to prevent
intimate partner violence and their related program evaluation
activities. CDC requests approval for 47 burden hours annually. There
is no cost to respondents other than their time.
[[Page 11991]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondent respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
DELTA Impact Program Key Informant 10 1 1 10
Recipients State Domestic Interview--Proj
Violence Coalitions. ect Lead (Att.
3).
Key Informant 10 1 45/60 8
Interview--Eval
uator (Att. 4).
Subrecipient 17 1 30/60 9
Survey (Att. 5).
Prevention 10 2 1 20
Infrastructure
Assessment
(Att. 6).
---------------------------------------------------------------------------------
Total..................... ................ .............. .............. .............. 47
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-04082 Filed 2-27-20; 8:45 am]
BILLING CODE 4163-18-P
