Proposed Data Collection Submitted for Public Comment and Recommendations, 11988-11990 [2020-04081]
Download as PDF
<![CDATA[
11988
Federal Register / Vol. 85, No. 40 / Friday, February 28, 2020 / Notices
Total Annual Responses: 2,908,096.
Total Burden Hours: 29,081.
Ms.
Shonna James, Director, Executive
Resources HR Services Center, Office of
Human Resources Management, General
Services Administration, 1800 F Street
NW, Washington, DC 20405, 202–230–
7005.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Section
4314 (c) (1) through (5) of title 5 U.S.C
requires each agency to establish, in
accordance with regulation prescribed
by the Office of Personnel Management,
one or more SES performance review
board(s). The board is responsible for
making recommendations to the
appointing and awarding authority on
the performance appraisal ratings and
performance awards for employees in
the Senior Executive Service.
The following have been designated
as members of the Performance Review
Board of GSA:
• Allison Azevedo, Acting Deputy
Commissioner, Public Buildings
Service.
• Allison Brigati, Deputy
Administrator—PRB Chair.
• Giancarlo Brizzi, Regional
Commissioner, Public Buildings
Service, Greater Southwest Region.
• Tiffany Hixson, Regional
Commissioner, Federal Acquisition
Service, Northwest, Arctic Region.
• Thomas Howder, Deputy
Commissioner, Federal Acquisition
Service.
• Merrick Krause, Acting Chief
Human Capital Officer, Office of Human
Resources Management.
• Jeffrey Lau, Regional
Commissioner, Federal Acquisition
Service, Northeast and Caribbean
Region.
• Jessica Salmoiraghi, Associate
Administrator for Governmentwide
Policy.
• Jack St. John, General Counsel.
Proposed Data Collection Submitted
for Public Comment and
Recommendations
FOR FURTHER INFORMATION CONTACT:
D. Public Comment
A. A 60-day notice was published in
the Federal Register at 84 FR 68455, on
December 16, 2019. One comment was
received; however, it did not change the
estimate of the burden.
Comment: The commenter expressed
support for the collection of data and
stated that it should be maintained and
enhanced given its essential role in
informing policy decisions surrounding
procurement and trade policy.
Response: This comment supports the
collection of information as necessary
for the proper performance of the
functions of Federal Government
acquisitions. It did not express an
opinion on whether the stated number
of burden hours is accurate for what
they believe to be the actual number of
hours an offeror expends to comply
with the provision.
Obtaining Copies: Requesters may
obtain a copy of the information
collection documents from the General
Services Administration, Regulatory
Secretariat Division (MVCB), 1800 F
Street NW, Washington, DC 20405,
telephone 202–501–4755. Please cite
OMB Control No. 9000–0161, Reporting
Purchases from Sources Outside the
United States, in all correspondence.
Dated: February 25, 2020.
Janet Fry,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2020–04110 Filed 2–27–20; 8:45 am]
BILLING CODE 6820–EP–P
GENERAL SERVICES
ADMINISTRATION
[Notice–CX–2020–01; Docket No. 2020–
0002; Sequence No. 8]
Office of Human Resources
Management; SES Performance
Review Board
Office of Human Resources
Management (OHRM), General Services
Administration (GSA).
ACTION: Notice.
AGENCY:
SUPPLEMENTARY INFORMATION:
Dated: February 21, 2020.
Emily W. Murphy,
Administrator, General Services
Administration.
[FR Doc. 2020–04105 Filed 2–27–20; 8:45 am]
jbell on DSKJLSW7X2PROD with NOTICES
17:27 Feb 27, 2020
Jkt 250001
PO 00000
[60Day–20–20IT; Docket No. CDC–2020–
0022]
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Understanding Long-term
Respiratory Morbidity in Former
Styrene-Exposed Workers. The purpose
of the interviews and medical testing is
to determine the prevalence of
respiratory symptoms and lung function
abnormalities among a cohort of former
styrene-exposed workers with different
exposure levels to evaluate the longterm impacts of styrene exposure on the
respiratory system.
DATES: CDC must receive written
comments on or before April 28, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0022 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
SUMMARY:
Please note: Submit all Federal comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
BILLING CODE 6820–FM–P
Notice is hereby given of the
appointment of new members to the
General Services Administration Senior
Executive Service Performance Review
Board. The Performance Review Board
assures consistency, stability, and
objectivity in the performance appraisal
process.
DATES: Applicable: February 28, 2020.
SUMMARY:
VerDate Sep<11>2014
Centers for Disease Control and
Prevention
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
FOR FURTHER INFORMATION CONTACT:
Frm 00043
Fmt 4703
Sfmt 4703
E:\FR\FM\28FEN1.SGM
28FEN1
11989
Federal Register / Vol. 85, No. 40 / Friday, February 28, 2020 / Notices
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. 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 submissions
of responses.
5. Assess information collection costs.
that workers previously exposed to high
concentrations of styrene (≥5 ppm),
even those with short tenure (<1 year),
will have a higher prevalence of
respiratory symptoms and lung function
abnormalities compared with workers
exposed to low concentration of styrene
(<5 ppm).
We will conduct face-to-face
interviews with members of a cohort of
workers from two reinforced plastic
boatbuilding plants that closed in 1989
and 1993. The purpose of the interviews
is to collect demographic information,
detailed job history during and after the
worker’s tenure at the boatbuilding
plant, upper and lower respiratory
symptoms, physician diagnoses of
respiratory diseases, cigarette smoking
history, and medication use. A NIOSH
employee will conduct the interviews.
We will also conduct several lung
function tests including: Exhaled nitric
oxide, impulse oscillometry, multiplebreath washout, spirometry,
bronchodilator reversibility testing, and
high-resolution computed tomography
(HRCT) scan.
The purpose of the lung function
testing is to identify small and large
airway abnormalities that are consistent
with NMRD. With the exception of the
HRCT scans, NIOSH technicians will
perform the lung function testing. An
accredited imaging center will be hired
to perform the HRCT scans. We will
collect blood to analyze for biomarkers
associated with lung injury caused by
obliterative bronchiolitis. A NIOSH
phlebotomist will collect the blood
samples. Finally, we will assess cohort
members for color vision abnormalities
using the Lanthony D–15 Color Test.
Color vision assessment will be
completed by a NIOSH technician. The
total estimated burden hours are 1,449.
There are no costs to respondents other
than their time.
Proposed Project
Understanding Long-term Respiratory
Morbidity in Former Styrene-Exposed
Workers—New—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Styrene is used in the production of
automobile parts, boats, computer
housings, food containers, wind energy
components, and many other products.
An estimated 90,000 U.S. workers are
potentially exposed to styrene at more
than 5,000 U.S. manufacturing plants.
Occupational exposure to styrene has
been associated with deleterious health
effects, including changes in color
vision, mucous membrane irritation,
hearing loss, and neurocognitive
impairment. Workplace exposure to
styrene has also been associated with
cases of non-malignant respiratory
disease (NMRD), including COPD and
obliterative bronchiolitis. However,
little is understood about the long-term
respiratory effects on styrene-exposed
workers. NIOSH is requesting a three
year OMB approval.
The goal of this project is to
understand the prevalence of long-term
respiratory morbidity in styreneexposed workers. The objectives of the
proposed study are: (1) To characterize
work exposures by acquiring job
histories and comparing with historical
exposure levels obtained from a past
industrial hygiene survey, (2) to
examine prevalence of respiratory
morbidity by duration and level of
styrene exposure and other
characteristics, (3) to apply research
biomarkers of lung injury to a styreneexposed workforce, and (4) to describe
the prevalence of color vision
impairment with the presence of
respiratory morbidity. Our hypothesis is
jbell on DSKJLSW7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Boatbuilder Cohort Members ............
Questionnaire and medical survey
consent form.
Questionnaire ...................................
Exhaled Nitric Oxide—no form ........
Impulse Oscillometry—no form ........
Spirometry—no form ........................
Bronchodilator Test—no form ..........
Multiple-Breath Washout—no form ..
Color vision test—no form ...............
Blood test—no form .........................
HRCT consent form .........................
HRCT Imaging—no form .................
Boatbuilder
Boatbuilder
Boatbuilder
Boatbuilder
Boatbuilder
Boatbuilder
Boatbuilder
Boatbuilder
Boatbuilder
Boatbuilder
Cohort
Cohort
Cohort
Cohort
Cohort
Cohort
Cohort
Cohort
Cohort
Cohort
VerDate Sep<11>2014
Members
Members
Members
Members
Members
Members
Members
Members
Members
Members
............
............
............
............
............
............
............
............
............
............
17:27 Feb 27, 2020
Jkt 250001
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
676
1
15/60
169
676
676
676
676
50
676
676
676
70
70
1
1
1
1
1
1
1
1
1
1
45/60
5/60
10/60
10/60
20/60
30/60
5/60
5/60
5/60
15/60
507
56
113
113
17
338
56
56
6
18
E:\FR\FM\28FEN1.SGM
28FEN1
11990
Federal Register / Vol. 85, No. 40 / Friday, February 28, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
..........................................................
........................
........................
........................
Type of respondents
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–04081 Filed 2–27–20; 8:45 am]
BILLING CODE 4163–18–P
Please Note: Submit all comments through
the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
FOR FURTHER INFORMATION CONTACT:
[60Day–20–20JC; Docket No. CDC–2020–
0023]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled ‘‘Delta Impact Cooperative
Agreement Evaluation Data Collection
Instruments’’, to collect information
from recipients related to program
evaluation activities for cooperative
agreement CDC–RFA–CE18–1801:
Domestic Violence Prevention
Enhancement and Leadership Through
Alliances (DELTA) Impact.
DATES: Written comments must be
received on or before April 28, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0023 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:27 Feb 27, 2020
Jkt 250001
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
Total burden
(in hours)
1,449
4. 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 submissions
of responses.
5. Assess information collection costs.
Proposed Project
Delta impact Cooperative Agreement
Evaluation Data Collection
Instruments—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) seeks OMB approval
for three years for a new information
collection request to collect information
from all 10 recipients (State Domestic
Violence Coalitions) and all 17
subrecipients (Coordinated Community
Response teams) funded through CDC’s
Domestic Violence Prevention
Enhancements and Leadership Through
Alliances (DELTA) Impact Program
cooperative agreement (NOFO CDC–
RFA–CE18–1801). CDC will collect
information from DELTA Impact
recipients as part of its program
evaluation to assess the implementation
and impact of the NOFO and further
understand the facilitators, barriers, and
critical factors to implement specific
violence prevention strategies and
conduct program evaluation activities.
The findings from this data collection
will be used for implementing and
evaluating DELTA Impact prevention
efforts, and will inform technical
assistance provided to recipients to
assist them in achieving the goals of the
DELTA Impact program. This data
collection will supplement other data to
highlight recipient and subrecipients’
experiences implementing their primary
prevention efforts to prevent intimate
partner violence and their related
program evaluation activities. CDC
requests approval for 47 burden hours
annually. There is no cost to
respondents other than their time.
E:\FR\FM\28FEN1.SGM
28FEN1
]]>Agencies
[Federal Register Volume 85, Number 40 (Friday, February 28, 2020)]
[Notices]
[Pages 11988-11990]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-04081]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-20-20IT; Docket No. CDC-2020-0022]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Understanding Long-term
Respiratory Morbidity in Former Styrene-Exposed Workers. The purpose of
the interviews and medical testing is to determine the prevalence of
respiratory symptoms and lung function abnormalities among a cohort of
former styrene-exposed workers with different exposure levels to
evaluate the long-term impacts of styrene exposure on the respiratory
system.
DATES: CDC must receive written comments on or before April 28, 2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0022 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, 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. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all Federal comments 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 Jeffrey M. Zirger, Information Collection
Review Office,
[[Page 11989]]
Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS-
D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: [email protected].
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 the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. 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
submissions of responses.
5. Assess information collection costs.
Proposed Project
Understanding Long-term Respiratory Morbidity in Former Styrene-
Exposed Workers--New--National Institute for Occupational Safety and
Health (NIOSH), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Styrene is used in the production of automobile parts, boats,
computer housings, food containers, wind energy components, and many
other products. An estimated 90,000 U.S. workers are potentially
exposed to styrene at more than 5,000 U.S. manufacturing plants.
Occupational exposure to styrene has been associated with deleterious
health effects, including changes in color vision, mucous membrane
irritation, hearing loss, and neurocognitive impairment. Workplace
exposure to styrene has also been associated with cases of non-
malignant respiratory disease (NMRD), including COPD and obliterative
bronchiolitis. However, little is understood about the long-term
respiratory effects on styrene-exposed workers. NIOSH is requesting a
three year OMB approval.
The goal of this project is to understand the prevalence of long-
term respiratory morbidity in styrene-exposed workers. The objectives
of the proposed study are: (1) To characterize work exposures by
acquiring job histories and comparing with historical exposure levels
obtained from a past industrial hygiene survey, (2) to examine
prevalence of respiratory morbidity by duration and level of styrene
exposure and other characteristics, (3) to apply research biomarkers of
lung injury to a styrene-exposed workforce, and (4) to describe the
prevalence of color vision impairment with the presence of respiratory
morbidity. Our hypothesis is that workers previously exposed to high
concentrations of styrene (>=5 ppm), even those with short tenure (<1
year), will have a higher prevalence of respiratory symptoms and lung
function abnormalities compared with workers exposed to low
concentration of styrene (<5 ppm).
We will conduct face-to-face interviews with members of a cohort of
workers from two reinforced plastic boatbuilding plants that closed in
1989 and 1993. The purpose of the interviews is to collect demographic
information, detailed job history during and after the worker's tenure
at the boatbuilding plant, upper and lower respiratory symptoms,
physician diagnoses of respiratory diseases, cigarette smoking history,
and medication use. A NIOSH employee will conduct the interviews. We
will also conduct several lung function tests including: Exhaled nitric
oxide, impulse oscillometry, multiple-breath washout, spirometry,
bronchodilator reversibility testing, and high-resolution computed
tomography (HRCT) scan.
The purpose of the lung function testing is to identify small and
large airway abnormalities that are consistent with NMRD. With the
exception of the HRCT scans, NIOSH technicians will perform the lung
function testing. An accredited imaging center will be hired to perform
the HRCT scans. We will collect blood to analyze for biomarkers
associated with lung injury caused by obliterative bronchiolitis. A
NIOSH phlebotomist will collect the blood samples. Finally, we will
assess cohort members for color vision abnormalities using the Lanthony
D-15 Color Test. Color vision assessment will be completed by a NIOSH
technician. The total estimated burden hours are 1,449. There are no
costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Boatbuilder Cohort Members.... Questionnaire 676 1 15/60 169
and medical
survey consent
form.
Boatbuilder Cohort Members.... Questionnaire... 676 1 45/60 507
Boatbuilder Cohort Members.... Exhaled Nitric 676 1 5/60 56
Oxide--no form.
Boatbuilder Cohort Members.... Impulse 676 1 10/60 113
Oscillometry--n
o form.
Boatbuilder Cohort Members.... Spirometry--no 676 1 10/60 113
form.
Boatbuilder Cohort Members.... Bronchodilator 50 1 20/60 17
Test--no form.
Boatbuilder Cohort Members.... Multiple-Breath 676 1 30/60 338
Washout--no
form.
Boatbuilder Cohort Members.... Color vision 676 1 5/60 56
test--no form.
Boatbuilder Cohort Members.... Blood test--no 676 1 5/60 56
form.
Boatbuilder Cohort Members.... HRCT consent 70 1 5/60 6
form.
Boatbuilder Cohort Members.... HRCT Imaging--no 70 1 15/60 18
form.
---------------------------------------------------------------------------------
[[Page 11990]]
Total..................... ................ .............. .............. .............. 1,449
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-04081 Filed 2-27-20; 8:45 am]
BILLING CODE 4163-18-P
