Proposed Data Collections Submitted for Public Comment and Recommendations, 24971-24973 [2017-11111]
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Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices
information contained in the notice
pursuant to exemption 4 of the Freedom
of Information Act (5 U.S.C. 552(b)(4)).
Board of Governors of the Federal Reserve
System, May 24, 2017.
Ann E. Misback,
Secretary of the Board.
[FR Doc. 2017–11136 Filed 5–30–17; 8:45 am]
Centers for Disease Control and
Prevention, Department of Health and
Human Services (HHS).
ACTION: Notice with comment period.
Change in Bank Control Notices;
Acquisitions of Shares of a Bank or
Bank Holding Company
nlaroche on DSK30NT082PROD with NOTICES
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed revision of the
information collection project titled
‘‘Health Hazard Evaluation and
Technical Assistance—Requests and
Emerging Problems.’’ This data
collection supports legislatively
mandated (PL 91–596) assistance
investigating emerging occupational
hazards in workplaces.
DATES: Written comments must be
received on or before July 31, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0050 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:
The notificants listed below have
applied under the Change in Bank
Control Act (12 U.S.C. 1817(j)) and
§ 225.41 of the Board’s Regulation Y (12
CFR 225.41) to acquire shares of a bank
or bank holding company. The factors
that are considered in acting on the
notices are set forth in paragraph 7 of
the Act (12 U.S.C. 1817(j)(7)).
The notices are available for
immediate inspection at the Federal
Reserve Bank indicated. The notices
also will be available for inspection at
the offices of the Board of Governors.
Interested persons may express their
views in writing to the Reserve Bank
indicated for that notice or to the offices
of the Board of Governors. Comments
must be received not later than June 19,
2017.
A. Federal Reserve Bank of
Minneapolis (Jacquelyn K. Brunmeier,
Assistant Vice President) 90 Hennepin
Avenue, Minneapolis, Minnesota
55480–0291:
1. Mark Edward Davis, Saint Peter,
Minnesota, Stanley M. Davis Revocable
Trust, Stanley Martin Davis, Trustee,
Plymouth, Minnesota, Martin Edward
Davis, Excelsior, Minnesota, Mark
Mitchell, Davis, Excelsior, Minnesota; as
a group acting in concert; to acquire the
voting shares of Bancommunity Services
Corporation, Saint Peter, Minnesota,
and thereby indirectly acquire voting
shares of First National Bank Minnesota,
Saint Peter, Minnesota
Board of Governors of the Federal Reserve
System, May 25, 2017.
Yao-Chin Chao,
Assistant Secretary of the Board.
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.
FOR FURTHER INFORMATION CONTACT:
BILLING CODE 6210–01–P
14:54 May 30, 2017
[60 Day–17–0260; Docket No. CDC–2017–
0050]
AGENCY:
FEDERAL RESERVE SYSTEM
VerDate Sep<11>2014
Centers for Disease Control and
Prevention
Proposed Data Collections Submitted
for Public Comment and
Recommendations
BILLING CODE 6210–01–P
[FR Doc. 2017–11209 Filed 5–30–17; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Jkt 241001
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
24971
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
Health Hazard Evaluation and
Technical Assistance—Requests and
Emerging Problems (OMB Control No.
E:\FR\FM\31MYN1.SGM
31MYN1
24972
Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices
0920–0260, Expiration 11/30/2017)—
Revision—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
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 290 such
requests. Most HHE requests come from
the following types of companies:
service, manufacturing, health and
social services, transportation,
agriculture, mining, skilled trade and
construction. NIOSH is requesting a
three year approval time.
A printed Health Hazard Evaluation
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 Health
Hazard Evaluation 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 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. When
an on-site evaluation is not done,
NIOSH prepares and provides a written
report after gathering information from
the requester(s) and reviewing available
exposure and health records.
In about 70% of on-site evaluations
(presently estimated to be 122 facilities
a year) employees are interviewed
individually to learn about health
problems and possible contributing
factors at work. 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 that involve employee
interviews (presently estimated to be 37
out of 122 facilities a year),
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 who agree
to participate wear a sampler or
monitoring device to measure personal
workplace exposures. They are offered
the opportunity to get a written notice
of their exposure results. To indicate
their preference, employees complete a
contact card. Completing a contact card
may take 5 minutes or less. The number
of employees monitored for workplace
exposures per on-site evaluation may
vary from none up to about 25. In some
instances, however, the number can be
much greater.
NIOSH distributes interim and final
reports of health hazard evaluations,
excluding personal identifiers, to:
Requesters, employers, employee
representatives; the Department of Labor
(Occupational Safety and Health
Administration or Mine Safety and
Health Administration, as appropriate);
state health departments; and, as
needed, other state and federal agencies.
NIOSH administers a follow-back
program to assess the effectiveness of its
HHE program in reducing workplace
hazards. NIOSH distributes follow-back
questionnaires to the primary employer
and employee representative at all the
workplaces where NIOSH conducted an
on-site evaluation. In a small number of
instances, a follow-back on-site
evaluation may be completed. The first
follow-back questionnaire is distributed
shortly after the first visit for an on-site
evaluation and takes about 10 minutes
to complete. A second follow-back
questionnaire is distributed a month
after the final report and requires about
20 minutes to complete. At 24 months,
a third follow-back questionnaire is
distributed which takes about 15
minutes to complete.
For requests where NIOSH does not
conduct an on-site evaluation, the
requestor receives the first follow-back
questionnaire 1 month after our report
and a second one 12 months after our
response. The first questionnaire takes
about 10 minutes to complete and the
second questionnaire takes about 15
minutes to complete.
Because of the number of
investigations conducted each year, the
need to respond quickly to requests for
assistance, the diverse and
unpredictable nature of these
investigations, and its follow-back
program to assess evaluation
effectiveness; NIOSH requests a
consolidated clearance for data
collections performed within the
domain of its HHE program. There is no
cost to respondents other than their
time. The total estimated annual burden
hours is 2,960.
ESTIMATE OF ANNUALIZED BURDEN HOURS
Number of
respondents
nlaroche on DSK30NT082PROD with NOTICES
Type of respondent
Form
Employees and Representatives .....
Health Hazard Evaluation Request
Form.
Health Hazard Evaluation Request
Form.
Health Hazard Evaluation specific
interview example.
Employers ........................................
Employees .......................................
VerDate Sep<11>2014
14:54 May 30, 2017
Jkt 241001
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
in hours
Total burden
hours
203
1
12/60
41
87
1
12/60
18
2,580
1
15/60
645
E:\FR\FM\31MYN1.SGM
31MYN1
24973
Federal Register / Vol. 82, No. 103 / Wednesday, May 31, 2017 / Notices
ESTIMATE OF ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Average
burden per
response
in hours
Number of
responses per
respondent
Total burden
hours
Type of respondent
Form
Employees .......................................
Health Hazard Evaluation specific
questionnaire example.
Contact information post card .........
First followback questionnaire .........
Second followback questionnaire ....
3,700
1
30/60
1,850
2,150
244
244
1
1
1
5/60
10/60
20/60
180
41
82
Third followback questionnaire ........
244
1
15/60
61
First followback questionnaire .........
98
1
10/60
17
Second followback questionnaire ....
98
1
15/60
25
..........................................................
........................
..........................
........................
2,960
Employees .......................................
Employees and Representatives;
Employers—Year 1 (on-site evaluation).
Employees and Representatives;
Employers—Year 2 (on-site evaluation).
Employees and Representatives;
Employers—Year 1 (without onsite evaluation).
Employees and Representatives;
Employers—Year 2 (without onsite evaluation).
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. 2017–11111 Filed 5–30–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–1036; Docket No. CDC–2017–
0051]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention, 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 take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on ‘‘Community Assessment
for Public Health Emergency Response
(CASPER).’’ CASPER is an effective
public health tool designed to quickly
provide low-cost, household-based
information about a community’s needs
and health status in a simple, easy-tounderstand format for decision makers.
nlaroche on DSK30NT082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
14:54 May 30, 2017
Jkt 241001
Written comments must be
received on or before July 31, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0051 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.
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
DATES:
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
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
E:\FR\FM\31MYN1.SGM
31MYN1
]]>Agencies
[Federal Register Volume 82, Number 103 (Wednesday, May 31, 2017)]
[Notices]
[Pages 24971-24973]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-11111]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-17-0260; Docket No. CDC-2017-0050]
Proposed Data Collections Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention, Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
revision of the information collection project titled ``Health Hazard
Evaluation and Technical Assistance--Requests and Emerging Problems.''
This data collection supports legislatively mandated (PL 91-596)
assistance investigating emerging occupational hazards in workplaces.
DATES: Written comments must be received on or before July 31, 2017.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2017-
0050 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.
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
Health Hazard Evaluation and Technical Assistance--Requests and
Emerging Problems (OMB Control No.
[[Page 24972]]
0920-0260, Expiration 11/30/2017)--Revision--National Institute for
Occupational Safety and Health (NIOSH), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
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 290 such
requests. Most HHE requests come from the following types of companies:
service, manufacturing, health and social services, transportation,
agriculture, mining, skilled trade and construction. NIOSH is
requesting a three year approval time.
A printed Health Hazard Evaluation 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 Health
Hazard Evaluation 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 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 on-site 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. When an on-site evaluation is not done, NIOSH
prepares and provides a written report after gathering information from
the requester(s) and reviewing available exposure and health records.
In about 70% of on-site evaluations (presently estimated to be 122
facilities a year) employees are interviewed individually to learn
about health problems and possible contributing factors at work.
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 that involve employee
interviews (presently estimated to be 37 out of 122 facilities a year),
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 who agree to participate wear a
sampler or monitoring device to measure personal workplace exposures.
They are offered the opportunity to get a written notice of their
exposure results. To indicate their preference, employees complete a
contact card. Completing a contact card may take 5 minutes or less. The
number of employees monitored for workplace exposures per on-site
evaluation may vary from none up to about 25. In some instances,
however, the number can be much greater.
NIOSH distributes interim and final reports of health hazard
evaluations, excluding personal identifiers, to: Requesters, employers,
employee representatives; the Department of Labor (Occupational Safety
and Health Administration or Mine Safety and Health Administration, as
appropriate); state health departments; and, as needed, other state and
federal agencies.
NIOSH administers a follow-back program to assess the effectiveness
of its HHE program in reducing workplace hazards. NIOSH distributes
follow-back questionnaires to the primary employer and employee
representative at all the workplaces where NIOSH conducted an on-site
evaluation. In a small number of instances, a follow-back on-site
evaluation may be completed. The first follow-back questionnaire is
distributed shortly after the first visit for an on-site evaluation and
takes about 10 minutes to complete. A second follow-back questionnaire
is distributed a month after the final report and requires about 20
minutes to complete. At 24 months, a third follow-back questionnaire is
distributed which takes about 15 minutes to complete.
For requests where NIOSH does not conduct an on-site evaluation,
the requestor receives the first follow-back questionnaire 1 month
after our report and a second one 12 months after our response. The
first questionnaire takes about 10 minutes to complete and the second
questionnaire takes about 15 minutes to complete.
Because of the number of investigations conducted each year, the
need to respond quickly to requests for assistance, the diverse and
unpredictable nature of these investigations, and its follow-back
program to assess evaluation effectiveness; NIOSH requests a
consolidated clearance for data collections performed within the domain
of its HHE program. There is no cost to respondents other than their
time. The total estimated annual burden hours is 2,960.
Estimate of Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form respondents responses per response in hours
respondent hours
----------------------------------------------------------------------------------------------------------------
Employees and Representatives Health Hazard 203 1 12/60 41
Evaluation
Request Form.
Employers.................... Health Hazard 87 1 12/60 18
Evaluation
Request Form.
Employees.................... Health Hazard 2,580 1 15/60 645
Evaluation
specific
interview
example.
[[Page 24973]]
Employees.................... Health Hazard 3,700 1 30/60 1,850
Evaluation
specific
questionnaire
example.
Employees.................... Contact 2,150 1 5/60 180
information
post card.
Employees and First followback 244 1 10/60 41
Representatives; Employers-- questionnaire. 244 1 20/60 82
Year 1 (on-site evaluation). Second
followback
questionnaire.
Employees and Third followback 244 1 15/60 61
Representatives; Employers-- questionnaire.
Year 2 (on-site evaluation).
Employees and First followback 98 1 10/60 17
Representatives; Employers-- questionnaire.
Year 1 (without on-site
evaluation).
Employees and Second 98 1 15/60 25
Representatives; Employers-- followback
Year 2 (without on-site questionnaire.
evaluation).
----------------------------------------------------------------
Total.................... ................ .............. ............... .............. 2,960
----------------------------------------------------------------------------------------------------------------
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. 2017-11111 Filed 5-30-17; 8:45 am]
BILLING CODE 4163-18-P
