Proposed Data Collection Submitted for Public Comment and Recommendations, 41963-41965 [2017-18697]
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Federal Register / Vol. 82, No. 170 / Tuesday, September 5, 2017 / Notices
Please cite OMB Control No. 3090–
XXXX, Inquiry/Request Instrument, in
all correspondence.
Jeffrey A. Koses,
Director, Office of Acquisition Policy, Office
of Government-wide Policy.
[FR Doc. 2017–18675 Filed 9–1–17; 8:45 am]
BILLING CODE 6820–61–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Patient Safety Organizations:
Voluntary Relinquishment From the
Quantros Patient Safety Center
Agency for Healthcare Research
and Quality (AHRQ), Department of
Health and Human Services (HHS).
ACTION: Notice of delisting.
AGENCY:
The Patient Safety Rule
authorizes AHRQ, on behalf of the
Secretary of HHS, to list as a PSO an
entity that attests that it meets the
statutory and regulatory requirements
for listing. A PSO can be ‘‘delisted’’ by
the Secretary if it is found to no longer
meet the requirements of the Patient
Safety Act and Patient Safety Rule,
when a PSO chooses to voluntarily
relinquish its status as a PSO for any
reason, or when a PSO’s listing expires.
AHRQ has accepted a notification of
voluntary relinquishment from the
Quantros Patient Safety Center of its
status as a PSO, and has delisted the
PSO accordingly.
DATES: The directories for both listed
and delisted PSOs are ongoing and
reviewed weekly by AHRQ. The
delisting was applicable at 12:00
Midnight ET (2400) on August 15, 2017.
ADDRESSES: Both directories can be
accessed electronically at the following
HHS Web site: https://
www.pso.ahrq.gov/listed.
FOR FURTHER INFORMATION CONTACT:
Eileen Hogan, Center for Quality
Improvement and Patient Safety, AHRQ,
5600 Fishers Lane, Room 06N94B,
Rockville, MD 20857; Telephone (toll
free): (866) 403–3697; Telephone (local):
(301) 427–1111; TTY (toll free): (866)
438–7231; TTY (local): (301) 427–1130;
Email: pso@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
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SUMMARY:
Background
The Patient Safety and Quality
Improvement Act of 2005, 42 U.S.C.
299b–21 to b–26, (Patient Safety Act)
and the related Patient Safety and
Quality Improvement Final Rule, 42
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CFR part 3 (Patient Safety Rule),
published in the Federal Register on
November 21, 2008, 73 FR 70732–
70814, establish a framework by which
hospitals, doctors, and other health care
providers may voluntarily report
information to Patient Safety
Organizations (PSOs), on a privileged
and confidential basis, for the
aggregation and analysis of patient
safety events.
The Patient Safety Act authorizes the
listing of PSOs, which are entities or
component organizations whose
mission and primary activity are to
conduct activities to improve patient
safety and the quality of health care
delivery.
HHS issued the Patient Safety Rule to
implement the Patient Safety Act.
AHRQ administers the provisions of the
Patient Safety Act and Patient Safety
Rule relating to the listing and operation
of PSOs. The Patient Safety Rule
authorizes AHRQ to list as a PSO an
entity that attests that it meets the
statutory and regulatory requirements
for listing. A PSO can be ‘‘delisted’’ if
it is found to no longer meet the
requirements of the Patient Safety Act
and Patient Safety Rule, when a PSO
chooses to voluntarily relinquish its
status as a PSO for any reason, or when
a PSO’s listing expires. Section 3.108(d)
of the Patient Safety Rule requires
AHRQ to provide public notice when it
removes an organization from the list of
federally approved PSOs.
AHRQ has accepted a notification
from the Quantros Patient Safety Center,
a component entity of Quantros Inc.,
PSO number P0014, to voluntarily
relinquish its status as a PSO.
Accordingly, the Quantros Patient
Safety Center was delisted effective at
12:00 Midnight ET (2400) on August 15,
2017.
The Quantros Patient Safety Center
has patient safety work product (PSWP)
in its possession. The PSO will meet the
requirements of section 3.108(c)(2)(i) of
the Patient Safety Rule regarding
notification to providers that have
reported to the PSO and of section
3.108(c)(2)(ii) regarding disposition of
PSWP consistent with section
3.108(b)(3). According to section
3.108(b)(3) of the Patient Safety Rule,
the PSO has 90 days from the effective
date of delisting and revocation to
complete the disposition of PSWP that
is currently in the PSO’s possession.
More information on PSOs can be
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41963
obtained through AHRQ’s PSO Web site
at https://www.pso.ahrq.gov.
Sharon B. Arnold,
Deputy Director.
[FR Doc. 2017–18707 Filed 9–1–17; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0765; Docket No. CDC–2017–
0062]
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 comment on proposed and/
or continuing information collections,
as required by the Paperwork Reduction
Act of 1995. This notice invites
comments on a request for an extension
of an approved information collection
entitled, CDC’s Fellowship Management
System. CDC uses the information
collected for processes that aid and
enhance the selection of fellowship
participants and host sites and to track
participant information that helps
strengthen the current, emerging, and
ever-changing public health workforce.
DATES: Written comments must be
received on or before November 6, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0062 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.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:
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Federal Register / Vol. 82, No. 170 / Tuesday, September 5, 2017 / Notices
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 Leroy A.
Richardson, 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 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
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FOR FURTHER INFORMATION CONTACT:
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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
Fellowship Management System
(OMB No. 0920–0765, expires 04/30/
2018)— Extension—Division of
Scientific Education and Professional
Development (DSEPD), Center for
Surveillance, Education, and Laboratory
Services (CSELS), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
DSEPD requests a three-year
extension to continue use of the CDC
Fellowship Management System (FMS)
for its electronic applications, host sites,
and directory processes that allow
individuals to apply to fellowships
online, allow public health agencies to
submit fellowship assignment proposals
online, and track applicant and alumni
information. CDC uses the FMS
application module to collect, process,
and manage data from nonfederal
applicants seeking training or public
health support services through CDC
fellowships, under the Office of
Management and Budget (OMB) control
number 0920–0765. FMS is key to
CDC’s ability to protect the public’s
health by supporting training
opportunities that strengthen the public
health workforce. In 2015, OMB
approval for revision was granted for
FMS for a 3-year period. Since 2015,
OMB has approved nonsubstantive
changes to FMS information collection
requests under the same OMB control
number, 0920–0765. These changes
were made to accurately reflect evolving
fellowship eligibility requirements,
provide clarification of existing
questions, efficiently and effectively
accommodate changing needs of host
organizations, and to account for the
addition of 150 new applicants to the
Science Ambassadors Fellowship. A 3year extension will allow all fellowship
applicants, public health agencies that
host fellowship participants, and
fellowship alumni the continued use of
FMS for submission of electronic data.
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The mission of DSEPD is to improve
health outcomes through a competent,
sustainable, and empowered public
health workforce. Professionals in
public health, epidemiology, medicine,
economics, information science,
veterinary medicine, nursing, public
policy, and other related professionals
seek opportunities, through CDC
fellowships, to broaden their
knowledge, and skills to improve the
science and practice of public health.
CDC fellows are assigned to state, tribal,
local, and territorial public health
agencies; federal government agencies,
including CDC and Department of
Health and Human Services’ (HHS)
operational divisions, such as Centers
for Medicare & Medicaid Services; and
to nongovernmental organizations,
including academic institutions, tribal
organizations, and private public health
organizations.
FMS allows CDC to electronically
collect and process fellowship
applications, fellowship assignment
proposals, and fellowship alumni
information from nonfederal persons.
FMS is a flexible and robust data
management system that is standardized
and tailored for each CDC fellowship,
collecting only the minimum amount of
information required, thereby
streamlining decision processes for CDC
and reducing burden for respondents.
Respondent types vary depending on
fellowship eligibility requirements, and
responses to FMS questions are
voluntary. CDC uses the information
FMS gathers to identify participants for
its fellowship programs and effectively
address each program’s needs and the
needs of the public. By allowing online
submissions of applications to
fellowships and proposals for
fellowship assignments, FMS can track
fellowship applicants, alumni, and
public health service agency employees
seeking to host and work with fellows,
all in one integrated database.
The annual burden table reflects
OMB-approved changes since 2015,
including the 150 new respondents
applying to Science Ambassadors and
changes for public health agency
representatives. No changes were made
relative to the FMS Alumni Directory or
the FMS Host Site Module. There is no
cost to respondents other than their
time.
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Federal Register / Vol. 82, No. 170 / Tuesday, September 5, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden time
per response
(in hours)
Frequency
of response
Average total
response
burden
(in hours)
Type of respondent
Form name
Fellowship Applicants ........................
FMS Application ...............................
Science Ambassadors .....................
FMS Alumni Directory ......................
FMS Host Site Module ....................
1,991
150
1,382
408
1
1
1
1
1.75
45/60
15/60
1.5
3,485
113
346
612
..........................................................
3,931
........................
........................
4,556
Fellowship Alumni .............................
Public Health Agency or Organization Staff.
Total ...........................................
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. 2017–18697 Filed 9–1–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10203 and
CMS–10346]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected; and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
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SUMMARY:
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Comments on the collection(s) of
information must be received by the
OMB desk officer by October 5, 2017.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions:
OMB, Office of Information and
Regulatory Affairs
Attention: CMS Desk Officer
Fax Number: (202) 395–5806 OR
Email: OIRA_submission@omb.eop.gov.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
Web site address at https://
www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
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. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
DATES:
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Fmt 4703
Sfmt 4703
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare Health
Outcomes Survey (HOS); Use: The
collection is necessary to hold Medicare
managed care contracts accountable for
the quality of care they deliver to
beneficiaries. This reporting
requirement allows us to obtain the
information necessary for proper
oversight of the Medicare Advantage
program. It is critical to our mission that
we collect and disseminate valid and
reliable information that can be used to
improve quality of care through
identification of quality improvement
opportunities, assist us in carrying out
our oversight responsibilities, and help
beneficiaries make an informed choice
among health plans. Form Number:
CMS–10203 (OMB control number:
0938–0701); Frequency: Yearly; Affected
Public: Individuals and households;
Number of Respondents: 739,959; Total
Annual Responses: 554,895; Total
Annual Hours: 183,115. (For policy
questions regarding this collection
contact Kimberly DeMichele at 410–
786–4286.)
2. Type of Information Collection
Request: Reinstatement with change of a
previously approved information
collection; Title of Information
Collection: Appeals of Quality Bonus
Payment Determinations; Use: Section
1853(o) of the Social Security Act
requires us to make Quality Bonus
Payments (QBPs) to Medicare
Advantage (MA) organizations that
achieve performance rating scores of at
least 4 stars under a five star rating
system. MA organizations have 10
calendar days from the date of CMS’
release of its QBP determinations to
request a technical report from CMS
E:\FR\FM\05SEN1.SGM
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]]>Agencies
[Federal Register Volume 82, Number 170 (Tuesday, September 5, 2017)]
[Notices]
[Pages 41963-41965]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-18697]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-17-0765; Docket No. CDC-2017-0062]
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 comment on proposed and/or continuing information
collections, as required by the Paperwork Reduction Act of 1995. This
notice invites comments on a request for an extension of an approved
information collection entitled, CDC's Fellowship Management System.
CDC uses the information collected for processes that aid and enhance
the selection of fellowship participants and host sites and to track
participant information that helps strengthen the current, emerging,
and ever-changing public health workforce.
DATES: Written comments must be received on or before November 6, 2017.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2017-
0062 by any of the following methods:
Federal eRulemaking Portal: Regulations.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.
[[Page 41964]]
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 Leroy A. Richardson, 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 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
Fellowship Management System (OMB No. 0920-0765, expires 04/30/
2018)-- Extension--Division of Scientific Education and Professional
Development (DSEPD), Center for Surveillance, Education, and Laboratory
Services (CSELS), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
DSEPD requests a three-year extension to continue use of the CDC
Fellowship Management System (FMS) for its electronic applications,
host sites, and directory processes that allow individuals to apply to
fellowships online, allow public health agencies to submit fellowship
assignment proposals online, and track applicant and alumni
information. CDC uses the FMS application module to collect, process,
and manage data from nonfederal applicants seeking training or public
health support services through CDC fellowships, under the Office of
Management and Budget (OMB) control number 0920-0765. FMS is key to
CDC's ability to protect the public's health by supporting training
opportunities that strengthen the public health workforce. In 2015, OMB
approval for revision was granted for FMS for a 3-year period. Since
2015, OMB has approved nonsubstantive changes to FMS information
collection requests under the same OMB control number, 0920-0765. These
changes were made to accurately reflect evolving fellowship eligibility
requirements, provide clarification of existing questions, efficiently
and effectively accommodate changing needs of host organizations, and
to account for the addition of 150 new applicants to the Science
Ambassadors Fellowship. A 3-year extension will allow all fellowship
applicants, public health agencies that host fellowship participants,
and fellowship alumni the continued use of FMS for submission of
electronic data.
The mission of DSEPD is to improve health outcomes through a
competent, sustainable, and empowered public health workforce.
Professionals in public health, epidemiology, medicine, economics,
information science, veterinary medicine, nursing, public policy, and
other related professionals seek opportunities, through CDC
fellowships, to broaden their knowledge, and skills to improve the
science and practice of public health. CDC fellows are assigned to
state, tribal, local, and territorial public health agencies; federal
government agencies, including CDC and Department of Health and Human
Services' (HHS) operational divisions, such as Centers for Medicare &
Medicaid Services; and to nongovernmental organizations, including
academic institutions, tribal organizations, and private public health
organizations.
FMS allows CDC to electronically collect and process fellowship
applications, fellowship assignment proposals, and fellowship alumni
information from nonfederal persons. FMS is a flexible and robust data
management system that is standardized and tailored for each CDC
fellowship, collecting only the minimum amount of information required,
thereby streamlining decision processes for CDC and reducing burden for
respondents. Respondent types vary depending on fellowship eligibility
requirements, and responses to FMS questions are voluntary. CDC uses
the information FMS gathers to identify participants for its fellowship
programs and effectively address each program's needs and the needs of
the public. By allowing online submissions of applications to
fellowships and proposals for fellowship assignments, FMS can track
fellowship applicants, alumni, and public health service agency
employees seeking to host and work with fellows, all in one integrated
database.
The annual burden table reflects OMB-approved changes since 2015,
including the 150 new respondents applying to Science Ambassadors and
changes for public health agency representatives. No changes were made
relative to the FMS Alumni Directory or the FMS Host Site Module. There
is no cost to respondents other than their time.
[[Page 41965]]
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average burden Average total
Number of Frequency of time per response
Type of respondent Form name respondents response response (in burden (in
hours) hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Fellowship Applicants.......................... FMS Application........................ 1,991 1 1.75 3,485
Science Ambassadors.................... 150 1 45/60 113
Fellowship Alumni.............................. FMS Alumni Directory................... 1,382 1 15/60 346
Public Health Agency or Organization Staff..... FMS Host Site Module................... 408 1 1.5 612
---------------------------------------------------------------
Total...................................... ....................................... 3,931 .............. .............. 4,556
--------------------------------------------------------------------------------------------------------------------------------------------------------
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. 2017-18697 Filed 9-1-17; 8:45 am]
BILLING CODE 4163-18-P
