Agency Forms Undergoing Paperwork Reduction Act Review, 40703-40704 [2016-14724]
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Federal Register / Vol. 81, No. 120 / Wednesday, June 22, 2016 / Notices
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. 2016–14725 Filed 6–21–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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Healthcare Infection Control Practices
Advisory Committee (HICPAC)
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) announce
the following meeting for the
aforementioned committee:
Times and Dates: 9:00 a.m.–5:00 p.m.,
EDT, July 14, 2016; 9:00 a.m.–12:00
p.m., EDT, July 15, 2016.
Place: Centers for Disease Control and
Prevention, Global Communications
Center, Building 19, Auditorium B, 1600
Clifton Road NE., Atlanta, Georgia
30333.
Status: Open to the public, limited
only by the space available. The meeting
room accommodates approximately 300
people. Please register for the meeting at
www.cdc.gov/hicpac.
Purpose: The Committee is charged
with providing advice and guidance to
the Director, Division of Healthcare
Quality Promotion, the Director,
National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
the Director, CDC, the Secretary, Health
and Human Services regarding (1) the
practice of healthcare infection
prevention and control; (2) strategies for
surveillance, prevention, and control of
infections, antimicrobial resistance, and
related events in settings where
healthcare is provided; and (3) periodic
updating of CDC guidelines and other
policy statements regarding prevention
of healthcare-associated infections and
healthcare-related conditions.
Matters for Discussion: The agenda
will include updates on CDC’s activities
for prevention of healthcare associated
infections (HAIs), updates on
antimicrobial stewardship, an update on
Draft Guideline for Prevention of
Infections in Healthcare Personnel, and
an update from the workgroup for
considerations on endoscope
reprocessing.
Agenda items are subject to change as
priorities dictate.
Contact Person for More Information:
Erin Stone, M.S., HICPAC, Division of
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40703
Healthcare Quality Promotion, NCEZID,
CDC, 1600 Clifton Road NE., Mailstop
A–07, Atlanta, Georgia 30333 Telephone
(404) 639–4045, Email: hicpac@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.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, Washington, DC 20503 or by fax
to (202) 395–5806. Written comments
should be received within 30 days of
this notice.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
Proposed Project
Health Risks from Using Private Wells
for Drinking Water—New — National
Center for Environmental Health
(NCEH), Centers for Disease Control and
Prevention (CDC).
[FR Doc. 2016–14788 Filed 6–21–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–16–16TL]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) 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; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
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Background and Brief Description
The Safe Drinking Water Act of 1974
(SDWA) ensures that most Americans
are provided access to water that meets
established public health standards.
However, for over 38 million Americans
who rely on private wells or other
drinking water not protected by the
SDWA (herein referred to as private
wells), that is not the case. There is no
comprehensive knowledge about the
locations of private wells, the
populations served by these sources,
potential contaminants that might be
present in private well water in specific
areas of the country, or the potential
health risks associated with drinking
water from these sources.
The purpose of this new generic
clearance information collection request
is to assess the health risks associated
with exposure to contaminants in
drinking water from private wells across
varied geographic areas of the United
States in partnership with the
requesting agency (state, territorial,
local, or tribal health department). The
information obtained from these
investigations will be used to describe
health risks from exposure to
contaminants in drinking water from
private wells within a defined time
period and geographic distribution. This
information will be used to inform
public health protection activities
conducted by the requesting agencies.
The respondents are defined as adults
at least 18 years old, who use private
wells for drinking water, who are
willing to receive and return a tap water
sampling kit and urine specimen kit or
to provide a blood specimen, and who
are willing to answer survey questions.
They will be recruited from geographic
areas of interest as defined by the
requesting agency.
Based on our historical activities, we
estimate that CDC will conduct up to 10
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Federal Register / Vol. 81, No. 120 / Wednesday, June 22, 2016 / Notices
investigations per year. Each
investigation will involve on average
200 respondents. The total time burden
is 2,084 hours. There will be no cost to
the respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hrs.)
Type of respondents
Form name
Adult at least 18 years old using a private
well for tap water.
Screening Form ..............................................
2,500
1
6/60
Questionnaire .................................................
Urine Specimen and Tap Water Sample Collection.
2,000
2,000
1
1
35/60
20/60
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.
OMB. FDA is withdrawing the proposed
collection of information that published
on June 2, 2016, at this time.
[FR Doc. 2016–14724 Filed 6–21–16; 8:45 am]
Dated: June 16, 2016.
Leslie Kux,
Associate Commissioner for Policy.
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[FR Doc. 2016–14722 Filed 6–21–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Health Resources and Services
Administration
[Docket No. FDA–2013–D–1543]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Guidance for
Industry on Nonproprietary Naming of
Biological Products; Withdrawal
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
This document withdraws a
Food and Drug Administration (FDA)
notice that published in the Federal
Register of June 2, 2016 (81 FR 35367).
DATES: This notice is withdrawn on June
22, 2016.
FOR FURTHER INFORMATION CONTACT:
Howard Muller, Center for Drug
Evaluation and Research (CDER), 10903
New Hampshire Ave., Bldg. 51, Rm.
6234, Silver Spring, MD 20993–0002,
301–796–3474.
SUPPLEMENTARY INFORMATION: FDA
published a notice in the Federal
Register of June 2, 2016, informing
interested parties that the proposed
collection of information entitled
‘‘Guidance for Industry on
Nonproprietary Naming of Biological
Products’’ had been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995
and inviting the public to submit
comments on the proposed collection to
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Health Resources and Services
Administration, HHS.
ACTION: Notice.
AGENCY:
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects (section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995), the
Health Resources and Services
Administration (HRSA) announces
plans to submit an Information
Collection Request (ICR), described
below, to the Office of Management and
Budget (OMB). Prior to submitting the
ICR to OMB, HRSA seeks comments
from the public regarding the burden
estimate, below, or any other aspect of
the ICR.
DATES: Comments on this ICR should be
received no later than August 22, 2016.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 14N–39, 5600 Fishers
Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
SUMMARY:
Withdrawal of notice.
SUMMARY:
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request
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or call the HRSA Information Collection
Clearance Officer at (301) 443–1984.
When
submitting comments or requesting
information, please include the
information request collection title for
reference.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title:
Data Collection Tool for State Offices of
Rural Health Grant Program
OMB No. 0915–0322—Extension
Abstract: The mission of the Federal
Office of Rural Health Policy (FORHP)
is to sustain and improve access to
quality care services for rural
communities. In its authorizing
language (section 711 of the Social
Security Act [42 U.S.C. 912]), Congress
charged FORHP with administering
grants, cooperative agreements, and
contracts to provide technical assistance
and other activities as necessary to
support activities related to improving
health care in rural areas. In accordance
with the Public Health Service Act,
section 338J (42 U.S.C. 254r), HRSA
proposes to continue the State Offices of
Rural Health (SORH) Grant Program—
Funding Opportunity Announcement
(FOA) and Forms for the Application.
The FOA is used by 50 states in
preparing applications for grants under
the SORH Grant Program of the Public
Health Service Act, and in preparing the
required report.
Need and Proposed Use of the
Information: FORHP seeks to continue
gathering information from grantees on
their efforts to provide technical
assistance to clients within their states.
SORH grantees submit a Technical
Assistance Report that includes: (1) The
total number of technical assistance
encounters provided directly by the
grantee, and (2) the total number of
unduplicated clients that received direct
technical assistance from the grantee.
The Technical Assistance Report is
submitted via the HRSA Electronic
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]]>Agencies
[Federal Register Volume 81, Number 120 (Wednesday, June 22, 2016)]
[Notices]
[Pages 40703-40704]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-14724]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-16-16TL]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for the proposed
information collection is published to obtain comments from the public
and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (a)
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; (b) Evaluate the
accuracy of the agencies estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (c) Enhance the quality, utility, and clarity of
the information to be collected; (d) Minimize the burden of the
collection of information on those who are to respond, including
through the use of appropriate automated, electronic, mechanical, or
other technological collection techniques or other forms of information
technology, e.g., permitting electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to omb@cdc.gov. Direct written comments
and/or suggestions regarding the items contained in this notice to the
Attention: CDC Desk Officer, Office of Management and Budget,
Washington, DC 20503 or by fax to (202) 395-5806. Written comments
should be received within 30 days of this notice.
Proposed Project
Health Risks from Using Private Wells for Drinking Water--New --
National Center for Environmental Health (NCEH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Safe Drinking Water Act of 1974 (SDWA) ensures that most
Americans are provided access to water that meets established public
health standards. However, for over 38 million Americans who rely on
private wells or other drinking water not protected by the SDWA (herein
referred to as private wells), that is not the case. There is no
comprehensive knowledge about the locations of private wells, the
populations served by these sources, potential contaminants that might
be present in private well water in specific areas of the country, or
the potential health risks associated with drinking water from these
sources.
The purpose of this new generic clearance information collection
request is to assess the health risks associated with exposure to
contaminants in drinking water from private wells across varied
geographic areas of the United States in partnership with the
requesting agency (state, territorial, local, or tribal health
department). The information obtained from these investigations will be
used to describe health risks from exposure to contaminants in drinking
water from private wells within a defined time period and geographic
distribution. This information will be used to inform public health
protection activities conducted by the requesting agencies.
The respondents are defined as adults at least 18 years old, who
use private wells for drinking water, who are willing to receive and
return a tap water sampling kit and urine specimen kit or to provide a
blood specimen, and who are willing to answer survey questions. They
will be recruited from geographic areas of interest as defined by the
requesting agency.
Based on our historical activities, we estimate that CDC will
conduct up to 10
[[Page 40704]]
investigations per year. Each investigation will involve on average 200
respondents. The total time burden is 2,084 hours. There will be no
cost to the respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hrs.)
----------------------------------------------------------------------------------------------------------------
Adult at least 18 years old using a Screening Form.......... 2,500 1 6/60
private well for tap water.
Questionnaire........... 2,000 1 35/60
Urine Specimen and Tap 2,000 1 20/60
Water Sample Collection.
----------------------------------------------------------------------------------------------------------------
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. 2016-14724 Filed 6-21-16; 8:45 am]
BILLING CODE 4163-18-P
