Proposed Data Collection Submitted for Public Comment and Recommendations, 42820-42822 [2015-17699]
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42820
Federal Register / Vol. 80, No. 138 / Monday, July 20, 2015 / Notices
2015. Registration instructions can be
found on the Web site https://
www.selectagents.gov.
ADDRESSES: The webcast will be
broadcast from the Centers for Disease
Control and Prevention’s facility, 1600
Clifton Road, Atlanta, GA 30333. This
will only be produced as a webcast,
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FOR FURTHER INFORMATION CONTACT:
CDC: Ms. Diane Martin, Division of
Select Agents and Toxins, Office of
Public Health Preparedness and
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and Prevention, 1600 Clifton Road, NE.,
MS A–46, Atlanta, GA 30329; phone:
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APHIS: Dr. Keith Wiggins, APHIS
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Dated: July 15, 2015.
Pamela J. Cox,
Director, Division of the Executive Secretariat,
Centers for Disease Control and Prevention.
Times And Dates: 1:00 p.m.–2:30
p.m., EDT, August 11, 2015
Place: This meeting will be held by
teleconference. To participate in the
teleconference, please dial (866) 763–
0273 Passcode: 6158968.
Status: This meeting is open to the
public, limited only by the availability
of telephone ports. The public is
welcome to participate during the
public comment period, which is
tentatively scheduled from 2:15 to 2:30
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Purpose: The Subcommittee will
provide advice to the CDC Director
through the ACD on strategic and other
health disparities and health equity
issues and provide guidance on
opportunities for CDC.
Matters For Discussion: The Health
Disparities Subcommittee members will
discuss progress toward implementation
of the Health Disparities Subcommittee
recommendations and discuss the
intersection of health disparities and
women’s health.
The agenda is subject to change as
priorities dictate.
Contact Person For More Information:
Leandris Liburd, Ph.D., M.P.H., M.A.,
Designated Federal Officer, Health
Disparities Subcommittee, Advisory
Committee to the Director, CDC, 1600
Clifton Road, NE., M/S K–77, Atlanta,
Georgia 30333 Telephone (770) 488–
8343, Email: LEL1@cdc.gov.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
[FR Doc. 2015–17734 Filed 7–17–15; 8:45 am]
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
BILLING CODE 4163–18–P
[FR Doc. 2015–17661 Filed 7–17–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
mstockstill on DSK4VPTVN1PROD with NOTICES
Centers for Disease Control and
Prevention
Advisory Committee to the Director
(ACD), Centers for Disease Control and
Prevention—Health Disparities
Subcommittee (HDS)
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting of the
aforementioned subcommittee:
VerDate Sep<11>2014
16:30 Jul 17, 2015
Jkt 235001
Centers for Disease Control and
Prevention
[60Day–15–15AUJ; Docket No. CDC–2015–
0056]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
ACTION:
Notice with comment period.
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 the Paul Coverdell
National Acute Stroke Program
(PCNASP) reporting system, which was
established to improve quality of care
for acute stroke patients from onset of
signs and symptoms through hospital
care and rehabilitation and recovery.
DATES: Written comments must be
received on or before September 18,
2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0056 by any of the following methods:
Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson,
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.
SUMMARY:
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.
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the 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
FOR FURTHER INFORMATION CONTACT:
E:\FR\FM\20JYN1.SGM
20JYN1
Federal Register / Vol. 80, No. 138 / Monday, July 20, 2015 / Notices
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.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
mstockstill on DSK4VPTVN1PROD with NOTICES
Proposed Project
Paul Coverdell National Acute Stroke
Program (PCNASP)—New—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Stroke is the fifth leading cause of
death in the United States and results in
approximately 130,000 deaths per year.
Additionally, approximately 800,000
stroke events are reported each year,
including approximately 250,000
VerDate Sep<11>2014
16:30 Jul 17, 2015
Jkt 235001
recurrent strokes. However, many
strokes are preventable, or their severity
can be reduced through coordinated
care that is delivered in a timely
manner.
Stroke outcomes depend upon the
rapid recognition of signs and
symptoms of stroke, prompt transport to
a treatment facility, and early
rehabilitation. Improving outcomes
requires a coordinated systems
approach involving pre-hospital care,
emergency department and hospital
care, rehabilitation, prevention of
complications, and ongoing secondary
prevention. Each care setting has unique
opportunities for improving the quality
of care provided and access to available
professional and clinical care at the
local level within a coordinated statebased system of care.
Through the Paul Coverdell National
Acute Stroke Program (PCNASP), CDC
has been continuously working to
measure and improve acute stroke care
using well-known quality improvement
strategies coupled with frequent
evaluation of results. PCNASP awardees
are state health departments who work
with participating hospitals and EMS
agencies in their jurisdictions to
improve quality of care for stroke
patients. State-based efforts include
identifying effective stroke treatment
centers and building capacity and
infrastructure to ensure that stroke
patients are routed to effective treatment
centers in a timely manner.
During initial cooperative agreement
cycles, PCNASP awardees focused on
in-hospital quality of care (QoC) issues
with technical assistance provided by
CDC. Through lessons learned during
this process and other supporting
evidence in the field, it has become
evident that it is also important to
examine pre- and post-hospital
transitions of care to link the entire
continuum of stroke care when
improving QoC for stroke patients.
The PCNASP will continue under a
new five-year cooperative agreement,
subject to available funding, to begin on
or around July 1, 2015. The new funding
period reflects additional emphasis on
pre-hospital quality of care as well as
the post-hospital transition of care
setting from hospital to home and the
next care provider. Therefore, awardees
will systematically collect and report
data on hospital capacity and all three
phases of the stroke care continuum.
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
42821
The new cooperative agreement
funding cycle will include pre-hospital
(EMS), in-hospital, and post-hospital
patient care data. Data to be collected
for pre- and in-hospital care closely
align with standards of The Joint
Commission (TJC), the American Heart
Association’s Get With The Guidelines
(GWTG) program, and the National
Emergency Medical Services
Information System (NEMSIS). CDC and
awardees will work on defining
performance measures for the posthospital transition of care setting. Data
from these three settings will be
transmitted from the awardees to CDC
quarterly. The average burden per
response for this data will vary between
30–90 minutes. The burden will be 30
minutes each for independent
submission of information relating to
the pre-hospital, in-hospital, and posthospital phases of patient care.
Alternatively, the burden will be 90
minutes for awardees who transmit
pre-, in-, and post-hospital data as one
combined file. CDC accepts file
transmissions as individual phases or
combined.
In addition, the new cooperative
agreement funding cycle will also
include primary data collection of
hospital inventory data to understand
the capacity and infrastructure of the
hospitals that admit and treat stroke
patients. Each hospital will report
inventory information to its PCNASP
awardee annually. The average burden
per response is 15 minutes. In addition,
each PCNASP awardee will prepare an
annual aggregate hospital inventory file
for transmission to CDC. The average
burden of reporting hospital inventory
information for each PCNASP awardee
is 8 hours per response. All patient,
hospital, and EMS provider data that is
submitted to CDC by PCNASP awardees
will be de-identified and occur through
secure data systems.
Proposed data elements and quality
indicators may be updated over time to
include new or revised items based on
evolving recommendations and
standards in the field to improve the
quality of stroke care.
OMB approval is requested for three
years. All information is submitted to
CDC electronically. Participation is
voluntary and there are no costs to
respondents other than their time.
E:\FR\FM\20JYN1.SGM
20JYN1
42822
Federal Register / Vol. 80, No. 138 / Monday, July 20, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hrs.)
Total burden
(in hrs.)
Type of respondent
Form name
PCNASP Awardee ............................
Hospital .............................................
Hospital Inventory ............................
In-hospital care data ........................
Pre-hospital care data ......................
Post-hospital transition of care data
Hospital Inventory ............................
9
9
9
9
400
1
4
4
4
1
8
30/60
30/60
30/60
15/60
72
18
18
18
100
Total ...........................................
...........................................................
........................
........................
........................
226
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2015–17699 Filed 7–17–15; 8:45 am]
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
Informational Meeting: The Importation
and Exportation of Infectious
Biological Agents, Infectious
Substances and Vectors; Public
Webcast
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of public webcast.
AGENCY:
The Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS) is hosting a public
webcast which will include
representatives from the U.S.
Department of Transportation, USDA
Animal and Plant Health Inspection
Services, CDC Division of Global
Migration and Quarantine, U.S. Customs
and Border Protection, U.S. Department
of Commerce, U.S. Food and Drug
Administration, HHS/Office of the
Assistant Secretary for Preparedness
and Response/Biomedical Advanced
Research and Development Authority.
This public webcast will address import
and export regulations for infectious
biological agents, infectious substances,
and vectors, and import and export
exemptions. The purpose of this notice
is to inform all interested parties,
including those individuals and entities
already possessing an import or export
permit (or license) of the webcast.
DATES: The webcast will be held on
September 16, 2015 from 11 a.m. to 4
p.m. EDT. Registration instructions are
mstockstill on DSK4VPTVN1PROD with NOTICES
VerDate Sep<11>2014
16:30 Jul 17, 2015
Jkt 235001
The webcast will be
broadcast from the Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., Atlanta, Georgia 30329.
ADDRESSES:
Von
McClee, Division of Select Agents and
Toxins, Office of Public Health
Preparedness and Response, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS A–46, Atlanta, GA
30333; phone: 404–718–2000; email:
lrsat@cdc.gov.
FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
SUMMARY:
found on the HHS/CDC’s Import Permit
Program Web site, https://www.cdc.gov/
od/eaipp/importApplication/
agents.htm.
This
webcast is an opportunity for the
regulated community (i.e., academic
institutions and biomedical centers,
commercial manufacturing facilities,
federal, state, and local laboratories,
including clinical and diagnostic
laboratories, research facilities,
exhibition facilities, and educational
facilities) and other interested
individuals to obtain specific regulatory
guidance and information regarding
import and export regulations. The
webcast will also provide assistance to
those interested in applying for an
import or export permit (or license)
from federal agencies within the United
States.
Instructions for registration are found
on the HHS/CDC’s Import Permit
Program Web site, https://www.cdc.gov/
od/eaipp/importApplication/
agents.htm. Participants must register
by September 2, 2015. This is a webcast
only event and there will be no on-site
participation at the HHS/CDC broadcast
facility.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Advisory Board on Radiation and
Worker Health (ABRWH or Advisory
Board), National Institute for
Occupational Safety and Health
(NIOSH)
Correction: This notice was published
in the Federal Register on June 30,
2015, Volume 80, Number 125, Pages
37263–37264. The time and date should
read as follows:
Time and Date: 8:15 a.m.–5:30 p.m.,
Mountain Time, July 23, 2015.
Public Comment Time and Date: 5:30
p.m.–6:30 p.m., Mountain Time, July 23,
2015.
Contact Person for More Information:
Theodore Katz, Designated Federal
Officer, NIOSH, CDC, 1600 Clifton Road
NE., MS E–20, Atlanta, Georgia 30333,
telephone: (513) 533–6800, toll free: 1–
800–CDC–INFO, email: dcas@cdc.gov.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2015–17704 Filed 7–17–15; 8:45 am]
BILLING CODE 4163–18–P
Dated: July 15, 2015.
Pamela J. Cox,
Director, Division of the Executive Secretariat,
Centers for Disease Control and Prevention.
[FR Doc. 2015–17735 Filed 7–17–15; 8:45 am]
BILLING CODE 4163–18–P
PO 00000
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E:\FR\FM\20JYN1.SGM
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Agencies
[Federal Register Volume 80, Number 138 (Monday, July 20, 2015)]
[Notices]
[Pages 42820-42822]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-17699]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-15AUJ; Docket No. CDC-2015-0056]
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 the Paul
Coverdell National Acute Stroke Program (PCNASP) reporting system,
which was established to improve quality of care for acute stroke
patients from onset of signs and symptoms through hospital care and
rehabilitation and recovery.
DATES: Written comments must be received on or before September 18,
2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0056 by any of the following methods:
Federal eRulemaking Portal: Regulation.gov. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson, 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 the 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
[[Page 42821]]
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.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; (d) ways to
minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services
to provide information. Burden means the total time, effort, or
financial resources expended by persons to generate, maintain, retain,
disclose or provide information to or for a Federal agency. This
includes the time needed to review instructions; to develop, acquire,
install and utilize technology and systems for the purpose of
collecting, validating and verifying information, processing and
maintaining information, and disclosing and providing information; to
train personnel and to be able to respond to a collection of
information, to search data sources, to complete and review the
collection of information; and to transmit or otherwise disclose the
information.
Proposed Project
Paul Coverdell National Acute Stroke Program (PCNASP)--New--
National Center for Chronic Disease Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Stroke is the fifth leading cause of death in the United States and
results in approximately 130,000 deaths per year. Additionally,
approximately 800,000 stroke events are reported each year, including
approximately 250,000 recurrent strokes. However, many strokes are
preventable, or their severity can be reduced through coordinated care
that is delivered in a timely manner.
Stroke outcomes depend upon the rapid recognition of signs and
symptoms of stroke, prompt transport to a treatment facility, and early
rehabilitation. Improving outcomes requires a coordinated systems
approach involving pre-hospital care, emergency department and hospital
care, rehabilitation, prevention of complications, and ongoing
secondary prevention. Each care setting has unique opportunities for
improving the quality of care provided and access to available
professional and clinical care at the local level within a coordinated
state-based system of care.
Through the Paul Coverdell National Acute Stroke Program (PCNASP),
CDC has been continuously working to measure and improve acute stroke
care using well-known quality improvement strategies coupled with
frequent evaluation of results. PCNASP awardees are state health
departments who work with participating hospitals and EMS agencies in
their jurisdictions to improve quality of care for stroke patients.
State-based efforts include identifying effective stroke treatment
centers and building capacity and infrastructure to ensure that stroke
patients are routed to effective treatment centers in a timely manner.
During initial cooperative agreement cycles, PCNASP awardees
focused on in-hospital quality of care (QoC) issues with technical
assistance provided by CDC. Through lessons learned during this process
and other supporting evidence in the field, it has become evident that
it is also important to examine pre- and post-hospital transitions of
care to link the entire continuum of stroke care when improving QoC for
stroke patients.
The PCNASP will continue under a new five-year cooperative
agreement, subject to available funding, to begin on or around July 1,
2015. The new funding period reflects additional emphasis on pre-
hospital quality of care as well as the post-hospital transition of
care setting from hospital to home and the next care provider.
Therefore, awardees will systematically collect and report data on
hospital capacity and all three phases of the stroke care continuum.
The new cooperative agreement funding cycle will include pre-
hospital (EMS), in-hospital, and post-hospital patient care data. Data
to be collected for pre- and in-hospital care closely align with
standards of The Joint Commission (TJC), the American Heart
Association's Get With The Guidelines (GWTG) program, and the National
Emergency Medical Services Information System (NEMSIS). CDC and
awardees will work on defining performance measures for the post-
hospital transition of care setting. Data from these three settings
will be transmitted from the awardees to CDC quarterly. The average
burden per response for this data will vary between 30-90 minutes. The
burden will be 30 minutes each for independent submission of
information relating to the pre-hospital, in-hospital, and post-
hospital phases of patient care. Alternatively, the burden will be 90
minutes for awardees who transmit pre-, in-, and post-hospital data as
one combined file. CDC accepts file transmissions as individual phases
or combined.
In addition, the new cooperative agreement funding cycle will also
include primary data collection of hospital inventory data to
understand the capacity and infrastructure of the hospitals that admit
and treat stroke patients. Each hospital will report inventory
information to its PCNASP awardee annually. The average burden per
response is 15 minutes. In addition, each PCNASP awardee will prepare
an annual aggregate hospital inventory file for transmission to CDC.
The average burden of reporting hospital inventory information for each
PCNASP awardee is 8 hours per response. All patient, hospital, and EMS
provider data that is submitted to CDC by PCNASP awardees will be de-
identified and occur through secure data systems.
Proposed data elements and quality indicators may be updated over
time to include new or revised items based on evolving recommendations
and standards in the field to improve the quality of stroke care.
OMB approval is requested for three years. All information is
submitted to CDC electronically. Participation is voluntary and there
are no costs to respondents other than their time.
[[Page 42822]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response (in (in hrs.)
respondent hrs.)
----------------------------------------------------------------------------------------------------------------
PCNASP Awardee................ Hospital 9 1 8 72
Inventory.
In-hospital care 9 4 30/60 18
data.
Pre-hospital 9 4 30/60 18
care data.
Post-hospital 9 4 30/60 18
transition of
care data.
Hospital...................... Hospital 400 1 15/60 100
Inventory.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 226
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2015-17699 Filed 7-17-15; 8:45 am]
BILLING CODE 4163-18-P