Agency Forms Undergoing Paperwork Reduction Act Review, 19336-19337 [2014-07779]
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19336
Federal Register / Vol. 79, No. 67 / Tuesday, April 8, 2014 / Notices
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Dated: April 1, 2014.
Richard Kronick,
AHRQ Director.
[FR Doc. 2014–07804 Filed 4–7–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Toxic Substances and
Disease Registry
[30-Day-14–14FA]
mstockstill on DSK4VPTVN1PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to 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.
VerDate Mar<15>2010
16:42 Apr 07, 2014
Jkt 232001
Proposed Project
State Surveillance under the National
Toxic Substance Incidents Program
(NTSIP)—NEW—Agency for Toxic
Substances and Disease Registry
(ATSDR).
Background and Brief Description
The Agency for Toxic Substances and
Disease Registry (ATSDR) is sponsoring
the National Toxic Substance Incidents
Program (NTSIP) to gather information
from many resources to protect people
from harm caused by spills and leaks of
toxic substances. The NTSIP
information will be used to help prevent
or reduce the harm caused by toxic
substance incidents. The NTSIP is
modeled partially after the Hazardous
Substances Emergency Events
Surveillance (HSEES) Program which
ran from 1992 to 2012 [OMB number:
0923–0008; expiration date 01/31/2012],
with additions suggested by
stakeholders to have a more complete
program. The NTSIP has three
components: A national database, state
surveillance, and the response team.
This information collection request is
focused on the state surveillance
component.
The NTSIP is the only federal public
health-based surveillance system to
coordinate the collection, collation,
analysis, and distribution of acute toxic
substance incidents data to public
health and safety practitioners. Because
thousands of acute spills occur annually
around the country, it is necessary to
establish this surveillance system to
describe the public health impacts on
the population of the United States. The
ATSDR is seeking a three-year approval
for the ongoing collection of information
for the state surveillance system.
The main objectives of this
information collection are to:
1. Describe toxic substance releases
and the public health consequences
associated with such releases within the
participating states,
2. Identify and prioritize
vulnerabilities in industry,
transportation, and communities as they
relate to toxic substance releases, and
3. Identify, develop, and promote
strategies that could prevent ongoing
and future exposures and resultant
health effects from toxic substance
releases.
The NTSIP surveillance system will
be incident-driven and all acute toxic
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Frm 00021
Fmt 4703
Sfmt 4703
substance incidents occurring within
participating states will be included.
A standardized set of data will be
collected by the NTSIP coordinator for
each incident. The NTSIP coordinator
may be a federal employee assigned to
the state health department or an
employee of the state health
department. State, but not federal,
NTSIP coordinators will incur
recordkeeping burden during two
phases.
During the first phase, the NTSIP
coordinators will rapidly collect and
enter data from a variety of existing data
sources. Examples of existing data
sources include, but are not limited to,
reports from the media, the National
Response Center, the U.S. Department of
Transportation Hazardous Materials
Information Reporting System, and state
environmental protection agencies.
Approximately 65% of the information
is expected to be obtained from existing
data sources.
The second phase of the information
collection will require the NTSIP
coordinators to alert other entities of the
incident when appropriate and to
request additional information to
complete the remaining unanswered
data fields. Approximately 35% of the
information is expected to be obtained
from calling, emailing, or faxing
additional types of respondents by the
NTSIP coordinators.
These additional respondents will
incur reporting burden and include, but
are not limited to, the on-scene
commander of the incident, emergency
government services (e.g., state
divisions of emergency management,
local emergency planning committees,
fire or Hazmat units, police, and
emergency medical services), the
responsible party (i.e., the ‘‘spiller’’),
other state and local government
agencies, hospitals and local poison
control centers.
The NTSIP coordinator will enter data
directly into an ATSDR internet-based
data system. NTSIP materials, including
a public use data set, annual report, and
published articles will be made
available on the ATSDR NTSIP Web
page at https://www.atsdr.cdc.gov/ntsip/.
There are no costs to respondents
other than their time. The total
estimated annual burden hours are
1,821.
E:\FR\FM\08APN1.SGM
08APN1
19337
Federal Register / Vol. 79, No. 67 / Tuesday, April 8, 2014 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
State NTSIP Coordinators ..............................
On-scene commanders ...................................
Emergency government services ...................
Responsible party ...........................................
Other state and local governments ................
Hospitals .........................................................
Poison Control Centers ...................................
LeRoy 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. 2014–07779 Filed 4–7–14; 8:45 am]
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Centers for Disease Control and
Prevention
[60Day–14–0260]
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Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 or send
comments to LeRoy Richardson, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
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; and (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. Written comments should
be received within 60 days of this
notice.
19:04 Apr 07, 2014
Jkt 232001
NTSIP
NTSIP
NTSIP
NTSIP
NTSIP
NTSIP
NTSIP
State
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State
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State
State
State
Data
Data
Data
Data
Data
Data
Data
Collection
Collection
Collection
Collection
Collection
Collection
Collection
Form
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Proposed Project
Health Hazard Evaluation and
Technical Assistance—Requests and
Emerging Problems (0920–0260,
Expiration 11/30/2014)—Revision—
National Institute for Occupational
Safety and Health (NIOSH), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
VerDate Mar<15>2010
Number of
respondents
Form name
In accordance with its mandates
under the Occupational Safety and
Health Act of 1970 and the Federal
Mine Safety and Health Act of 1977, the
National Institute for Occupational
Safety and Health (NIOSH) responds to
requests for health hazard evaluations
(HHE) to identify chemical, biological or
physical hazards in workplaces
throughout the United States. Each year,
NIOSH receives approximately 300 such
requests. Most HHE requests come from
the following types of companies:
Service, manufacturing, health and
social services, transportation,
construction, agriculture, mining,
skilled trade and construction.
A printed HHE request form is
available in English and in Spanish. The
form is also available on the Internet
and differs from the printed version
only in format and in the fact that it can
be submitted directly from the Web site.
The request form takes an estimated 12
minutes to complete. The form provides
the mechanism for employees,
employers, and other authorized
representatives to supply the
information required by the regulations
governing the NIOSH HHE program (42
CFR 85.3–1). If employees are
submitting the form, it must contain the
signatures of three or more current
employees. However, regulations allow
a single signature if the requestor: Is one
of three (3) or fewer employees in the
process, operation, or job of concern; or
is any officer of a labor union
representing the employees for
collective bargaining purposes. An
individual management official may
request an evaluation on behalf of the
employer. The information provided is
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Sfmt 4703
3
110
810
15
60
10
80
Number of
responses per
respondent
426
1
1
1
1
1
1
Average
burden per
response
(in hrs.)
1
30/60
30/60
30/60
30/60
30/60
30/60
used by NIOSH to determine whether
there is reasonable cause to justify
conducting an investigation and
provides a mechanism to respond to the
requestor.
NIOSH reviews the HHE request to
determine if an on-site evaluation is
needed. The primary purpose of an onsite evaluation is to help employers and
employees identify and eliminate
occupational health hazards. For 40% of
the requests received NIOSH determines
an on-site evaluation is needed.
In about 70% of on-site evaluations,
employees are interviewed to help
further define concerns. Interviews may
take approximately 15 minutes per
respondent. The interview questions are
specific to each workplace and its
suspected diseases and hazards.
However, interviews are based on
standard medical practices.
In approximately 30% of on-site
evaluations (presently estimated to be
38 facilities), questionnaires are
distributed to the employees (averaging
about 100 employees per site).
Questionnaires may require
approximately 30 minutes to complete.
The survey questions are specific to
each workplace and its suspected
diseases and hazards, however, items in
the questionnaires are derived from
standardized or widely used medical
and epidemiologic data collection
instruments.
About 70% of the on-site evaluations
involve employee exposure monitoring
in the workplace. Employees
participating in on-site evaluations by
wearing a sampler or monitoring device
to measure personal workplace
exposures are offered the opportunity to
get a written notice of their exposure
results. To indicate their preference and,
if interested, provide mailing
information, employees complete a
contact information post card. The
previous approved information
collection request has been revised to
include the post card, which may take
5 minutes or less to complete. The
number of employees monitored for
E:\FR\FM\08APN1.SGM
08APN1
Agencies
[Federal Register Volume 79, Number 67 (Tuesday, April 8, 2014)]
[Notices]
[Pages 19336-19337]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-07779]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Toxic Substances and Disease Registry
[30-Day-14-14FA]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
(404) 639-7570 or send an email to omb@cdc.gov. Send written comments
to 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
State Surveillance under the National Toxic Substance Incidents
Program (NTSIP)--NEW--Agency for Toxic Substances and Disease Registry
(ATSDR).
Background and Brief Description
The Agency for Toxic Substances and Disease Registry (ATSDR) is
sponsoring the National Toxic Substance Incidents Program (NTSIP) to
gather information from many resources to protect people from harm
caused by spills and leaks of toxic substances. The NTSIP information
will be used to help prevent or reduce the harm caused by toxic
substance incidents. The NTSIP is modeled partially after the Hazardous
Substances Emergency Events Surveillance (HSEES) Program which ran from
1992 to 2012 [OMB number: 0923-0008; expiration date 01/31/2012], with
additions suggested by stakeholders to have a more complete program.
The NTSIP has three components: A national database, state
surveillance, and the response team. This information collection
request is focused on the state surveillance component.
The NTSIP is the only federal public health-based surveillance
system to coordinate the collection, collation, analysis, and
distribution of acute toxic substance incidents data to public health
and safety practitioners. Because thousands of acute spills occur
annually around the country, it is necessary to establish this
surveillance system to describe the public health impacts on the
population of the United States. The ATSDR is seeking a three-year
approval for the ongoing collection of information for the state
surveillance system.
The main objectives of this information collection are to:
1. Describe toxic substance releases and the public health
consequences associated with such releases within the participating
states,
2. Identify and prioritize vulnerabilities in industry,
transportation, and communities as they relate to toxic substance
releases, and
3. Identify, develop, and promote strategies that could prevent
ongoing and future exposures and resultant health effects from toxic
substance releases.
The NTSIP surveillance system will be incident-driven and all acute
toxic substance incidents occurring within participating states will be
included.
A standardized set of data will be collected by the NTSIP
coordinator for each incident. The NTSIP coordinator may be a federal
employee assigned to the state health department or an employee of the
state health department. State, but not federal, NTSIP coordinators
will incur recordkeeping burden during two phases.
During the first phase, the NTSIP coordinators will rapidly collect
and enter data from a variety of existing data sources. Examples of
existing data sources include, but are not limited to, reports from the
media, the National Response Center, the U.S. Department of
Transportation Hazardous Materials Information Reporting System, and
state environmental protection agencies. Approximately 65% of the
information is expected to be obtained from existing data sources.
The second phase of the information collection will require the
NTSIP coordinators to alert other entities of the incident when
appropriate and to request additional information to complete the
remaining unanswered data fields. Approximately 35% of the information
is expected to be obtained from calling, emailing, or faxing additional
types of respondents by the NTSIP coordinators.
These additional respondents will incur reporting burden and
include, but are not limited to, the on-scene commander of the
incident, emergency government services (e.g., state divisions of
emergency management, local emergency planning committees, fire or
Hazmat units, police, and emergency medical services), the responsible
party (i.e., the ``spiller''), other state and local government
agencies, hospitals and local poison control centers.
The NTSIP coordinator will enter data directly into an ATSDR
internet-based data system. NTSIP materials, including a public use
data set, annual report, and published articles will be made available
on the ATSDR NTSIP Web page at https://www.atsdr.cdc.gov/ntsip/.
There are no costs to respondents other than their time. The total
estimated annual burden hours are 1,821.
[[Page 19337]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hrs.)
----------------------------------------------------------------------------------------------------------------
State NTSIP Coordinators.............. NTSIP State Data 3 426 1
Collection Form.
On-scene commanders................... NTSIP State Data 110 1 30/60
Collection Form.
Emergency government services......... NTSIP State Data 810 1 30/60
Collection Form.
Responsible party..................... NTSIP State Data 15 1 30/60
Collection Form.
Other state and local governments..... NTSIP State Data 60 1 30/60
Collection Form.
Hospitals............................. NTSIP State Data 10 1 30/60
Collection Form.
Poison Control Centers................ NTSIP State Data 80 1 30/60
Collection Form.
----------------------------------------------------------------------------------------------------------------
LeRoy 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. 2014-07779 Filed 4-7-14; 8:45 am]
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