Request for Public Comment: 60-Day Notice for Extension of Fast Track Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery: IHS Customer Service Satisfaction and Similar Surveys, 11206-11208 [2015-04112]
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Federal Register / Vol. 80, No. 40 / Monday, March 2, 2015 / Notices
• Introduction of Ex-Offico and
Advisory Members.
• Report on the French Centenary.
• Discussion of recommendations to
be made to the Congress and the
President.
• World War 1 Washington Memorial
Report.
• Fund Raising Report.
• Education Report.
• Kansas City Memorial Day
invitation.
In this case, the agency is giving less
than 15 days’ notice due to the inability
to have quorum for the meeting.
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.
Dated: February 23, 2015.
Daniel S. Dayton,
Designated Federal Official, World War I
Centennial Commission.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2015–04247 Filed 2–27–15; 8:45 am]
[FR Doc. 2015–04210 Filed 2–27–15; 8:45 am]
BILLING CODE 6820–95–P
BILLING CODE 4163–18–P
Background
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Commission, 701 Pennsylvania Avenue
NW., 123, Washington, DC 20004–2608,
telephone number 202–380–0725 (Note:
This is not a toll-free number).
Written comments may be submitted
to the Commission and will be made
part of the permanent record of the
Commission. Comments must be
received by 5:00 p.m. Eastern Standard
Time (EST), Friday, March 6, 2015 and
may be provided by email to
daniel.dayton@
worldwar1centennial.org. Requests to
comment at the meeting must be
received by 5:00 p.m. Eastern Standard
Time (EST), Friday, March 6, 2015.
Written presentations may be provided
to Mr. Dayton at daniel.dayton@
worldwar1centennial.org until Friday,
March 6, 2015. Please contact Mr.
Dayton at the email address above to
obtain meeting materials.
SUPPLEMENTARY INFORMATION:
Centers for Disease Control and
Prevention
The World War One Centennial
Commission was established by Public
Law 112–272, as a commission to
ensure a suitable observance of the
centennial of World War I, to provide
for the designation of memorials to the
service of members of the United States
Armed Forces in World War I, and for
other purposes. Under this authority,
the Committee will plan, develop, and
execute programs, projects, and
activities to commemorate the
centennial of World War I, encourage
private organizations and State and
local governments to organize and
participate in activities commemorating
the centennial of World War I, facilitate
and coordinate activities throughout the
United States relating to the centennial
of World War I, serve as a clearinghouse
for the collection and dissemination of
information about events and plans for
the centennial of World War I, and
develop recommendations for Congress
and the President for commemorating
the centennial of World War I. The
Commission does not have an
appropriation and is operated solely on
donated funds.
Contact Daniel S. Dayton at
daniel.dayton@worldwar1centennial.org
to register to comment in person during
the meeting’s 30 minute public
comment period. Registered speakers/
organizations will be allowed 5 minutes
and will need to provide written copies
of their presentations.
Agenda: Thursday, March 12, 2015.
Old Business:
• Approval of minutes of previous
meetings.
• Public Comment Period.
New Business:
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Subcommittee for Dose
Reconstruction Reviews (SDRR),
Advisory Board on Radiation and
Worker Health (ABRWH or the
Advisory Board), National Institute for
Occupational Safety and Health
(NIOSH)
Notice of Cancellation: A notice was
published in the Federal Register on
January 30, 2015, Volume 80, Number
20, Page 5117, announcing an Audio
Conference Call of the ABRWH–SDRR
on February 27, 2015. This meeting was
canceled due to a lack of quorum for the
meeting. Notice will be provided when
the meeting is rescheduled in
accordance with section 10(a)(2) of the
Federal Advisory Committee Act (Pub.
L. 92–463).
Contact Person for More Information:
Theodore Katz, Designated Federal
Officer, NIOSH, CDC, 1600 Clifton
Road, Mailstop E–20, Atlanta Georgia
30333, Telephone (513) 533–6800, Toll
Free 1 (800) CDC–INFO, Email ocas@
cdc.gov.
This notice is published less than the
required 15 days prior to the start of the
announced meeting, in accordance with
Section 102–3.150(b) of the GSA Final
Rule (2001) that allows for exceptions to
the meeting notification time
requirement. Section 102–3.150(b) states
the following: ‘‘In exceptional
circumstances, the agency or an
independent Presidential advisory
committee may give less than 15
calendar days’’ notice, provided that the
reasons for doing so are included in the
advisory committee meeting notice
published in the Federal Register.’’
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Indian Health Service
Request for Public Comment: 60-Day
Notice for Extension of Fast Track
Generic Clearance for the Collection of
Qualitative Feedback on Agency
Service Delivery: IHS Customer
Service Satisfaction and Similar
Surveys
Indian Health Service, HHS.
Notice and request for
comments. Request for extension of
approval.
AGENCY:
ACTION:
The Indian Health Service
(IHS), as part of its continuing effort to
reduce paperwork and respondent
burden, invites the general public to
take this opportunity to comment on the
‘‘Generic Clearance for the Collection of
Qualitative Feedback on Agency Service
Delivery’’ for approval under the
Paperwork Reduction Act (PRA) (44
U.S.C. 3501 et. seq.). This collection was
developed as part of a Federal
Government-wide effort to streamline
the process for seeking feedback from
the public on service delivery. This
notice announces our intent to submit
this collection to the Office of
Management and Budget (OMB) for
approval and solicits comments on
specific aspects for the proposed
information collection. A copy of the
draft supporting statement is available
at www.regulations.gov (see Docket ID
[IHS–2015–0002]).
DATES: Consideration will be given to all
comments received by May 1, 2015.
ADDRESSES: Submit comments to
Tamara Clay by one of the following
methods:
• Mail: Tamara Clay, Information
Collection Clearance Officer, Indian
Health Service, 801 Thompson Avenue,
SUMMARY:
E:\FR\FM\02MRN1.SGM
02MRN1
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Federal Register / Vol. 80, No. 40 / Monday, March 2, 2015 / Notices
TMP, STE 450–30, Rockville, MD
20852.
• Phone: 301–443–4750.
• Email: Tamara.Clay@ihs.gov.
• Fax: 301–443–4750.
Comments submitted in response to
this notice will be made available to the
public by publishing them in the 30 day
Federal Register notice for this
information collection. For this reason,
please do not include information of a
confidential nature, such as sensitive
personal information or proprietary
information. If comments are submitted
via email, the email address will be
automatically captured and included as
part of the comment that is placed in the
public docket and made available on the
Internet. Please note that responses to
this public comment request containing
any routine notice about the
confidentiality of the communication
will be treated as public comments that
may be made available to the public
notwithstanding the inclusion of the
routine notice.
FOR FURTHER INFORMATION CONTACT:
Tamara Clay through:
• Mail: Tamara Clay, Information
Collection Clearance Officer, Indian
Health Service, 801 Thompson Avenue,
TMP, STE 450–30, Rockville, MD
20852.
• Phone: 301–443–4750.
• Email: Tamara.Clay@ihs.gov.
• Fax: 301–443–4750.
SUPPLEMENTARY INFORMATION: Title:
Generic Clearance for the Collection of
Qualitative Feedback on Agency Service
Delivery: IHS Customer Service
Satisfaction and Similar Surveys.
Abstract: The proposed information
collection activity provides a means to
garner qualitative customer and
stakeholder feedback in an efficient,
timely manner, in accordance with the
Administration’s commitment to
improving service delivery. Qualitative
feedback is information that provides
useful insights on perceptions and
opinions, but is not statistical surveys
that yield quantitative results that can
be generalized to the population of
study. This feedback will provide
insights into customer or stakeholder
perceptions, experiences and
expectations, provide an early warning
of issues with service, or focus attention
on areas where communication, training
or changes in operations might improve
delivery of products or services. These
collections will allow for ongoing,
collaborative and actionable
communications between the Agency
and its customers and stakeholders. It
will also allow feedback to contribute
directly to the improvement of program
management.
VerDate Sep<11>2014
16:55 Feb 27, 2015
Jkt 235001
The solicitation of feedback will target
areas such as: Timeliness,
appropriateness, accuracy of
information, courtesy, efficiency of
service delivery, and resolution of
issues with service delivery. Responses
will be assessed to plan and inform
efforts to improve or maintain the
quality of service offered to the public.
If this information is not collected, vital
feedback from customers and
stakeholders on the agency’s services
will be unavailable.
The agency will only submit a
collection for approval under this
generic clearance if it meets the
following conditions:
• The collections are voluntary;
• The collections are low-burden for
respondents (based on considerations of
total burden hours, total number of
respondents, or burden-hours per
respondent) and are low-cost for both
the respondents and the Federal
Government;
• The collections are noncontroversial and do not raise issues of
concern to other Federal agencies;
• Any collection is targeted to the
solicitation of opinions from
respondents who have experience with
the program or may have experience
with the program in the near future;
• Personally identifiable information
is collected only to the extent necessary
and is not retained;
• Information gathered will be used
only internally for general service
improvement and program management
purposes and is not intended for release
outside of the agency;
• Information gathered will not be
used for the purpose of substantially
informing influential policy decisions;
and
• Information gathered will yield
qualitative information; the collections
will not be designed or expected to
yield statistically reliable results or used
as though the results are generalizable to
the population of study.
Feedback collected under this generic
clearance provides useful information,
but it does not yield data that can be
generalized to the overall population.
This type of generic clearance for
qualitative information will not be used
for quantitative information collections
that are designed to yield reliably
actionable results, such as monitoring
trends over time or documenting
program performance. Such data uses
require more rigorous designs that
address: The target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
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11207
sample size, the expected response rate,
methods for assessing potential nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior to
fielding the study. Depending on the
degree of influence the results are likely
to have, such collections may still be
eligible for submission for other generic
mechanisms that are designed to yield
quantitative results.
As a general matter, information
collections will not result in any new
system of records containing privacy
information and will not ask questions
of a sensitive nature, such as sexual
behavior and attitudes, religious beliefs,
and other matters that are commonly
considered private.
Current Actions: Extension of
approval for a collection of information.
Type of Review: Extension.
Affected Public: Individuals and
households, businesses and
organizations, and Tribal governments.
Estimated Number of Respondents:
105,000.
Below are projected annual average
estimates for the next three years:
Average Expected Annual Number of
Activities: 100.
Average Number of Respondents per
Activity: 1,050.
Annual Responses: 105,000.
Frequency of Response: Once per
request.
Average Minutes per Response: 10.
Burden Hours: 17,500.
Request for Comments: Comments
submitted in response to this notice will
be summarized and/or included in the
request for OMB approval. Comments
are invited on: (a) Whether the
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
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
E:\FR\FM\02MRN1.SGM
02MRN1
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Federal Register / Vol. 80, No. 40 / Monday, March 2, 2015 / Notices
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.
All written comments will be
available for public inspection on
Regulations.gov.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number.
Comment Due Date: Your comments
regarding this information collection are
best assured of having full effect if
received within 30 days of the date of
this publication.
a useful alcohol biosensor in the near
future. The NIH believes that this
challenge will stimulate investment
from public and private sectors in the
development of functional alcohol
biosensors that will be appealing to
individuals, treatment providers, and
researchers.
DATES:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Submission period begins March 2,
2015, 9:00 a.m. ET.
Submission period ends: December 1,
2015.
Judging period: January 2016.
Winners announced: On or after
February 15, 2016.
The NIH will announce any changes
to this timeline by amending this
Federal Register notice.
FOR FURTHER INFORMATION CONTACT: M.
Katherine Jung, Ph.D., Program Director,
Division of Metabolism and Health
Effects, National Institute on Alcohol
Abuse and Alcoholism, Phone: 301–
443–8744, Email Kathy.jung@nih.gov.
F.L. Dammann, M.P.A., Management
Analyst and Special Assistant to the
Executive, National Institute on Alcohol
Abuse and Alcoholism, Phone: 301–
480–9433, Email: fl.dammann@nih.gov.
SUPPLEMENTARY INFORMATION:
National Institutes of Health
Subject of Challenge
Dated: February 20, 2015.
Robert G. McSwain,
Acting Director, Indian Health Service.
[FR Doc. 2015–04112 Filed 2–27–15; 8:45 am]
BILLING CODE 4165–16–P
Announcement of Requirements and
Registration for ‘‘A Wearable Alcohol
Biosensor’’ Challenge
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Authority: 15 U.S.C. 3719.
Award Approving Official: Dr.
Lawrence A. Tabak, Principal Deputy
Director, National Institutes of Health
(NIH).
SUMMARY: Through the ‘‘A Wearable
Alcohol Biosensor’’ Challenge (the
‘‘Challenge’’), the National Institute on
Alcohol Abuse and Alcoholism
(NIAAA), a component of the National
Institutes of Health (NIH), is searching
for a wearable or otherwise discreet
device capable of measuring blood
alcohol level in real time. The advent of
alcohol biosensors that can be worn
discreetly and used by individuals in
the course of their daily lives will
advance the mission of NIAAA in the
arenas of research, treatment, and
rehabilitation. NIAAA has supported
academic and small business grants and
contracts to advance the development
and use of alcohol biosensors in the
past. Current technological
developments in electronics,
miniaturization, wireless technology,
and biophysical techniques of alcohol
detection in humans increase the
likelihood of successful development of
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16:55 Feb 27, 2015
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Current technologies for real time
monitoring of alcohol consumption,
used in criminal justice applications,
have performed adequately, but have
disadvantages for broader use.
NIAAA seeks the design and
production of a wearable device to
monitor blood alcohol levels in real
time. The device should be
inconspicuous, low profile, and
appealing to the wearer. The design can
take the form of jewelry, clothing, or any
other format located in contact with the
human body. A non-invasive technology
is preferred.
Current technology for continuous
alcohol monitoring takes a reading every
30 minutes. We are seeking a solution
that improves on this interval and most
closely approximates real time
monitoring and data collection. The
device should be able to quantitate
blood alcohol level, interpret and store
the data, or transmit it to a smartphone
or other device by wireless
transmission. Data storage and
transmission must be completely secure
in order to protect the privacy of the
individual. The device should have the
ability to verify standardization at
regular intervals and to indicate loss of
functionality. The power source should
be dependable and rechargeable. A form
of subject identification would be an
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added benefit. The device can be
removable.
This is a reduction to practice
challenge that requires written
documentation and a working prototype
of the submitted solution.
NIAAA is open to a range of design
forms which can accomplish the above
tasks.
Statutory Authority of the Funding
Source
This Challenge is consistent with and
advances the mission of NIAAA, as
described in 42 U.S.C. 285n, to conduct
and support biomedical and behavioral
research, health services research,
research training, and health
information dissemination with respect
to the prevention of alcohol abuse and
the treatment of alcoholism, and to
conduct a study of alternative
approaches for alcoholism and alcohol
abuse treatment and rehabilitation.
Eligibility Rules for the Challenge
1. To Participate
This Challenge is open to any
‘‘Solver’’ where ‘‘Solver’’ is defined as
an individual, a group of individuals
(i.e., a team), or an entity. Whether
singly or as part of a group or entity,
individuals younger than 18
participating in the Challenge must
provide parental consent and must
abide by the Children’s Online Privacy
Protection Act.
2. To Win
To be eligible to win a prize under
this Challenge, the Solver—
1. Shall have registered to participate
in the Challenge at www.challenge.gov.
2. Shall have complied with all the
requirements under this section on
Eligibility.
3. In the case of a private entity, shall
be incorporated in and maintain a
primary place of business in the United
States; and in the case of an individual,
whether participating singly or in a
group, shall be a citizen or permanent
resident of the United States. Note: NonU.S. citizens and nonpermanent
residents can participate as a member of
a team that otherwise satisfies the
eligibility criteria but will not be eligible
to win a monetary prize (in whole or in
part); however, their participation as
part of a winning team, if applicable,
may be recognized when results are
announced.
4. In the case of an individual, he/she
may not be an employee of the NIH; an
individual involved in formulation of
the Challenge and/or serving on the
technical evaluation panel; any other
individual involved with the design,
E:\FR\FM\02MRN1.SGM
02MRN1
]]>Agencies
[Federal Register Volume 80, Number 40 (Monday, March 2, 2015)]
[Notices]
[Pages 11206-11208]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-04112]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Indian Health Service
Request for Public Comment: 60-Day Notice for Extension of Fast
Track Generic Clearance for the Collection of Qualitative Feedback on
Agency Service Delivery: IHS Customer Service Satisfaction and Similar
Surveys
AGENCY: Indian Health Service, HHS.
ACTION: Notice and request for comments. Request for extension of
approval.
-----------------------------------------------------------------------
SUMMARY: The Indian Health Service (IHS), as part of its continuing
effort to reduce paperwork and respondent burden, invites the general
public to take this opportunity to comment on the ``Generic Clearance
for the Collection of Qualitative Feedback on Agency Service Delivery''
for approval under the Paperwork Reduction Act (PRA) (44 U.S.C. 3501
et. seq.). This collection was developed as part of a Federal
Government-wide effort to streamline the process for seeking feedback
from the public on service delivery. This notice announces our intent
to submit this collection to the Office of Management and Budget (OMB)
for approval and solicits comments on specific aspects for the proposed
information collection. A copy of the draft supporting statement is
available at www.regulations.gov (see Docket ID [IHS-2015-0002]).
DATES: Consideration will be given to all comments received by May 1,
2015.
ADDRESSES: Submit comments to Tamara Clay by one of the following
methods:
Mail: Tamara Clay, Information Collection Clearance
Officer, Indian Health Service, 801 Thompson Avenue,
[[Page 11207]]
TMP, STE 450-30, Rockville, MD 20852.
Phone: 301-443-4750.
Email: Tamara.Clay@ihs.gov.
Fax: 301-443-4750.
Comments submitted in response to this notice will be made
available to the public by publishing them in the 30 day Federal
Register notice for this information collection. For this reason,
please do not include information of a confidential nature, such as
sensitive personal information or proprietary information. If comments
are submitted via email, the email address will be automatically
captured and included as part of the comment that is placed in the
public docket and made available on the Internet. Please note that
responses to this public comment request containing any routine notice
about the confidentiality of the communication will be treated as
public comments that may be made available to the public
notwithstanding the inclusion of the routine notice.
FOR FURTHER INFORMATION CONTACT: Tamara Clay through:
Mail: Tamara Clay, Information Collection Clearance
Officer, Indian Health Service, 801 Thompson Avenue, TMP, STE 450-30,
Rockville, MD 20852.
Phone: 301-443-4750.
Email: Tamara.Clay@ihs.gov.
Fax: 301-443-4750.
SUPPLEMENTARY INFORMATION: Title: Generic Clearance for the Collection
of Qualitative Feedback on Agency Service Delivery: IHS Customer
Service Satisfaction and Similar Surveys. Abstract: The proposed
information collection activity provides a means to garner qualitative
customer and stakeholder feedback in an efficient, timely manner, in
accordance with the Administration's commitment to improving service
delivery. Qualitative feedback is information that provides useful
insights on perceptions and opinions, but is not statistical surveys
that yield quantitative results that can be generalized to the
population of study. This feedback will provide insights into customer
or stakeholder perceptions, experiences and expectations, provide an
early warning of issues with service, or focus attention on areas where
communication, training or changes in operations might improve delivery
of products or services. These collections will allow for ongoing,
collaborative and actionable communications between the Agency and its
customers and stakeholders. It will also allow feedback to contribute
directly to the improvement of program management.
The solicitation of feedback will target areas such as: Timeliness,
appropriateness, accuracy of information, courtesy, efficiency of
service delivery, and resolution of issues with service delivery.
Responses will be assessed to plan and inform efforts to improve or
maintain the quality of service offered to the public. If this
information is not collected, vital feedback from customers and
stakeholders on the agency's services will be unavailable.
The agency will only submit a collection for approval under this
generic clearance if it meets the following conditions:
The collections are voluntary;
The collections are low-burden for respondents (based on
considerations of total burden hours, total number of respondents, or
burden-hours per respondent) and are low-cost for both the respondents
and the Federal Government;
The collections are non-controversial and do not raise
issues of concern to other Federal agencies;
Any collection is targeted to the solicitation of opinions
from respondents who have experience with the program or may have
experience with the program in the near future;
Personally identifiable information is collected only to
the extent necessary and is not retained;
Information gathered will be used only internally for
general service improvement and program management purposes and is not
intended for release outside of the agency;
Information gathered will not be used for the purpose of
substantially informing influential policy decisions; and
Information gathered will yield qualitative information;
the collections will not be designed or expected to yield statistically
reliable results or used as though the results are generalizable to the
population of study.
Feedback collected under this generic clearance provides useful
information, but it does not yield data that can be generalized to the
overall population. This type of generic clearance for qualitative
information will not be used for quantitative information collections
that are designed to yield reliably actionable results, such as
monitoring trends over time or documenting program performance. Such
data uses require more rigorous designs that address: The target
population to which generalizations will be made, the sampling frame,
the sample design (including stratification and clustering), the
precision requirements or power calculations that justify the proposed
sample size, the expected response rate, methods for assessing
potential non-response bias, the protocols for data collection, and any
testing procedures that were or will be undertaken prior to fielding
the study. Depending on the degree of influence the results are likely
to have, such collections may still be eligible for submission for
other generic mechanisms that are designed to yield quantitative
results.
As a general matter, information collections will not result in any
new system of records containing privacy information and will not ask
questions of a sensitive nature, such as sexual behavior and attitudes,
religious beliefs, and other matters that are commonly considered
private.
Current Actions: Extension of approval for a collection of
information.
Type of Review: Extension.
Affected Public: Individuals and households, businesses and
organizations, and Tribal governments.
Estimated Number of Respondents: 105,000.
Below are projected annual average estimates for the next three
years:
Average Expected Annual Number of Activities: 100.
Average Number of Respondents per Activity: 1,050.
Annual Responses: 105,000.
Frequency of Response: Once per request.
Average Minutes per Response: 10.
Burden Hours: 17,500.
Request for Comments: Comments submitted in response to this notice
will be summarized and/or included in the request for OMB approval.
Comments are invited on: (a) Whether the 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 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
[[Page 11208]]
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.
All written comments will be available for public inspection on
Regulations.gov.
An agency may not conduct or sponsor, and a person is not required
to respond to, a collection of information unless it displays a
currently valid OMB control number.
Comment Due Date: Your comments regarding this information
collection are best assured of having full effect if received within 30
days of the date of this publication.
Dated: February 20, 2015.
Robert G. McSwain,
Acting Director, Indian Health Service.
[FR Doc. 2015-04112 Filed 2-27-15; 8:45 am]
BILLING CODE 4165-16-P
