Proposed Data Collection Submitted for Public Comment and Recommendations, 26116-26117 [2019-11649]
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26116
Federal Register / Vol. 84, No. 108 / Wednesday, June 5, 2019 / Notices
The BGMIS does not collect data related
to assessing aggregate outcomes. A
separate information collection request,
designed to assess cross-cutting outputs
and outcomes resulting from Block grant
has been developed and is undergoing
public comment.
Legislation requires awardees to be
accountable for funds they receive by
evaluating and reporting on program
activities and health status on an annual
basis. The BGMIS system allows CDC
and awardees to measure performance,
identifying the extent to which
objectives were met and identifying the
most highly successful program
interventions. CDC requests OMB
approval to continue the Block Grant
information collection for three years.
CDC will continue to use the BGMIS to
monitor awardee progress, identify
activities and personnel supported with
Block Grant funding, conduct
compliance reviews of Block Grant
awardees, and promote the use of
evidence-based guidelines and
interventions. There are no changes to
the number of respondents or the
estimated annual burden per
respondent. The Work Plan and the
Annual Report will be submitted
annually. The estimated burden per
response for the Work Plan is 20 hours
and the estimated burden per response
for the Annual Report is 15 hours.
Participation in this information
collection is required for Block Grant
awardees. There are no costs to
respondents other than their time.
Awardees continue to submit Success
Stories with their Annual Progress
reports through BGMIS, without
changes.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
PHHS Block Grant Coordinator ......................
PHHS Block Grant Coordinator ......................
Work Plan .......................................................
Annual Report ................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–11645 Filed 6–4–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–19–19AXA; Docket No. CDC–2019–
0046]
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 efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection entitled ‘‘Annual Reporting of
the Rape Prevention and Education
(RPE) Program: CE19–1902 Cooperative
Agreement.’’ Information will be
collected annually from RPE recipients
and will provide crucial data for
SUMMARY:
jbell on DSK3GLQ082PROD with NOTICES
Number of
respondents
Type of respondents
VerDate Sep<11>2014
19:03 Jun 04, 2019
Jkt 247001
performance monitoring and program
evaluation of the implementation of
prevention strategies and approaches,
outcomes, and budget of the cooperative
agreement.
DATES: Written comments must be
received on or before August 5, 2019.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0046 by any of the following methods:
Federal eRulemaking Portal:
Regulation.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. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment
should be submitted 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: omb@cdc.gov.
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
61
61
Number of
responses per
respondent
1
1
Average
burden per
response
(in hours)
20
15
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 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,
SUPPLEMENTARY INFORMATION:
E:\FR\FM\05JNN1.SGM
05JNN1
26117
Federal Register / Vol. 84, No. 108 / Wednesday, June 5, 2019 / Notices
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Annual Reporting of the Rape
Prevention and Education (RPE)
Program: CE19–1902 Cooperative
Agreement—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
OMB approval is requested for three
years for this new collection. The RPE
Program, which provides funding to
health departments in all 50 states, the
District of Columbia (DC), Puerto Rico,
Guam, the U.S. Virgin Islands, and the
Commonwealth of Northern Mariana
Islands. This ICR will collect
information related to implementation
strategies, outcomes, evaluation, and
state action plan.
Collecting information about the
implementation and outcomes of CE19–
1902 cooperative agreement through the
online data system, DVP Partners Portal,
is crucial to informing Sexual Violence
prevention nationally; enhancing
accountability of the use of federal
funds; providing timely program reports
and responses to information requests,
such as Congressional requests
mandated by the authorizing legislation;
improving real-time communications
between CDC and RPE recipients; and
strengthening CDC’s capacity to provide
responsive data-driven technical
assistance and to monitor and evaluate
recipients’ progress and performance.
The only cost to respondents will be
time spent responding to the survey/
screener. The total estimated annualized
burden hours is 440.
and outcomes annually from recipients
of the new funding opportunity CDC–
RFA–CE19–1902: Rape Prevention and
Education (RPE): Using The Best
Available Evidence for Sexual Violence
Prevention cooperative agreement. This
new RPE funding opportunity differs
greatly from previous funding
opportunities provided by CDC through
the RPE Program. Specifically, program
activities differ from the previous
funding cycles, and the program will be
collecting information for the first time
on recipient outcomes.
RPE Program recipients or designated
delegates will submit data annually into
the online data system, DVP Partners
Portal. Recipients will monitor and
report progress on their goals,
objectives, and activities, as well as
relevant information on the
implementation of their prevention
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Total burden
(in hours)
Form name
RPE-funded Health Departments
(State, DC, and Territories) and
their Designated Delegates.
Annual Reporting—Initial Population
55
1
4
220
Annual Reporting—Subsequent Reporting.
55
2
2
220
...........................................................
........................
........................
........................
440
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–11649 Filed 6–4–19; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–1726–N]
Medicare Program; the Announcement
of the Annual Advisory Panel on
Hospital Outpatient Payment (HOP
Panel) Meeting in August 2019 and
New Panel Members
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice of meeting.
AGENCY:
jbell on DSK3GLQ082PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Type of respondents
This notice announces the
annual public meeting of the Advisory
Panel on Hospital Outpatient Payment
(the Panel) for 2019. In addition, it
announces 6 new membership
SUMMARY:
VerDate Sep<11>2014
19:03 Jun 04, 2019
Jkt 247001
appointments to the Panel. The purpose
of the Panel is to advise the Secretary of
the Department of Health and Human
Services and the Administrator of the
Centers for Medicare & Medicaid
Services concerning the clinical
integrity of the Ambulatory Payment
Classification groups and their
associated weights, and supervision of
hospital outpatient therapeutic services.
The recommendations provided by the
Panel will be considered as we prepare
the annual updates for the hospital
outpatient prospective payment system.
DATES:
Meeting Dates: The public meeting is
scheduled for Monday, August 19, 2019,
from 9:30 a.m. to 5:00 p.m. Eastern
Daylight Time (EDT), and Tuesday,
August 20, 2019, from 9:30 a.m. to 12:00
p.m. Eastern Daylight Time (EDT). The
times listed in this notice are
approximate times. Consequently, the
meetings may last longer or be shorter
than the times listed in this notice but
will not begin before the posted times.
Deadline for Meeting Registration,
Presentations and Comments:
Presentations or comments, and form
CMS–20017 (located at https://
PO 00000
Frm 00054
Fmt 4703
Sfmt 4703
www.cms.gov/Medicare/CMS-Forms/
CMS-Forms/downloads/cms20017.pdf)
must be received by 5:00 p.m. EDT on
Monday, July 22, 2019. Form CMS–
20017 must accompany each
presentation or comment submission.
Presentations and comments that are not
received by the due date and time or
that do not include a completed form
CMS–20017 will be considered late or
incomplete and will not be included on
the agenda. In commenting, refer to file
code CMS–1726–N.
Meeting Registration Timeframe:
Monday, June 24, 2019, through
Monday, July 29, 2019 at 5 p.m. EDT.
Participants planning to attend this
meeting in person must register online,
during the specified timeframe at:
https://www.cms.gov/apps/events/
default.asp.
On this web page, double click the
‘‘Upcoming Events’’ hyperlink, and then
double click the ‘‘HOP Panel’’ event title
link and enter the required information.
Include any requests for special
accommodations. Note: Participants
who do not plan to attend the meeting
in person should not register. No
registration is required for participants
E:\FR\FM\05JNN1.SGM
05JNN1
]]>Agencies
[Federal Register Volume 84, Number 108 (Wednesday, June 5, 2019)]
[Notices]
[Pages 26116-26117]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-11649]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-19-19AXA; Docket No. CDC-2019-0046]
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 efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection entitled ``Annual Reporting of the Rape
Prevention and Education (RPE) Program: CE19-1902 Cooperative
Agreement.'' Information will be collected annually from RPE recipients
and will provide crucial data for performance monitoring and program
evaluation of the implementation of prevention strategies and
approaches, outcomes, and budget of the cooperative agreement.
DATES: Written comments must be received on or before August 5, 2019.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2019-
0046 by any of the following methods:
Federal eRulemaking Portal: Regulation.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. All relevant comments received will be posted
without change to Regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to Regulations.gov.
Please note: All public comment should be submitted 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 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,
[[Page 26117]]
e.g., permitting electronic submissions of responses.
5. Assess information collection costs.
Proposed Project
Annual Reporting of the Rape Prevention and Education (RPE)
Program: CE19-1902 Cooperative Agreement--New--National Center for
Injury Prevention and Control (NCIPC), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
OMB approval is requested for three years for this new collection.
The RPE Program, which provides funding to health departments in all 50
states, the District of Columbia (DC), Puerto Rico, Guam, the U.S.
Virgin Islands, and the Commonwealth of Northern Mariana Islands. This
ICR will collect information related to implementation and outcomes
annually from recipients of the new funding opportunity CDC-RFA-CE19-
1902: Rape Prevention and Education (RPE): Using The Best Available
Evidence for Sexual Violence Prevention cooperative agreement. This new
RPE funding opportunity differs greatly from previous funding
opportunities provided by CDC through the RPE Program. Specifically,
program activities differ from the previous funding cycles, and the
program will be collecting information for the first time on recipient
outcomes.
RPE Program recipients or designated delegates will submit data
annually into the online data system, DVP Partners Portal. Recipients
will monitor and report progress on their goals, objectives, and
activities, as well as relevant information on the implementation of
their prevention strategies, outcomes, evaluation, and state action
plan.
Collecting information about the implementation and outcomes of
CE19-1902 cooperative agreement through the online data system, DVP
Partners Portal, is crucial to informing Sexual Violence prevention
nationally; enhancing accountability of the use of federal funds;
providing timely program reports and responses to information requests,
such as Congressional requests mandated by the authorizing legislation;
improving real-time communications between CDC and RPE recipients; and
strengthening CDC's capacity to provide responsive data-driven
technical assistance and to monitor and evaluate recipients' progress
and performance. The only cost to respondents will be time spent
responding to the survey/screener. The total estimated annualized
burden hours is 440.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
RPE-funded Health Departments Annual 55 1 4 220
(State, DC, and Territories) Reporting--Init
and their Designated ial Population.
Delegates.
Annual 55 2 2 220
Reporting--Subs
equent
Reporting.
---------------------------------------------------------------------------------
Total..................... ................ .............. .............. .............. 440
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-11649 Filed 6-4-19; 8:45 am]
BILLING CODE 4163-19-P
