Proposed Data Collection Submitted for Public Comment and Recommendations, 7560-7562 [2020-02541]
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7560
Federal Register / Vol. 85, No. 27 / Monday, February 10, 2020 / Notices
monitoring. This information includes
an Environmental Public Health
Tracking Workplan Template, a
Performance Measure Report, a
Communication Plan, a Partnership
Plan, and a website Analytics Template.
Each of these forms are collected
annually as documents emailed to the
Tracking Program. A public health
action (PHA) report is submitted at least
once and up to four times a year via
email to the Tracking Program as funded
SLHD have PHA to report.
Over the past three years, these data
were used to identify funded SLHD in
some cases, the data at the source are
centralized and easily extracted. In
other cases, like for radon data, the data
are not. In those cases, the number of
hours for extracting and standardizing
the data is much greater. Four
respondents have been added to the 26
SLHDs the program currently funds to
account for the data voluntarily received
from unfunded SLHDs and to allow for
potential program growth over the next
three years.
need of additional technical assistance,
identify common challenges and
successes, improve communication
between funded SLHD and CDC, and to
monitor funded SLHD compliance with
funding requirements.
There are no costs for the respondents
other than their time. The total
estimated time burden is 21,860 hours.
This estimate includes the time it takes
to extract the data from the original data
source(s), standardize and format the
data to match the corresponding
Tracking Network data form, and submit
the data to the Tracking Network. In
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Avg. burden
per response
(in hrs.)
Total burden
(in hrs.)
Form name
State and local health departments ..
Birth defects prevalence ..................
Childhood lead blood levels .............
Community drinking water monitoring.
Emergency department visits ...........
Hospitalizations ................................
Radon testing ...................................
Metadata records .............................
EPHT Work Plan ..............................
Public Health Action Report .............
Performance Measure Report ..........
Communications plan .......................
Partnership plan ...............................
Website analytics .............................
22
18
30
1
1
1
80
80
100
1760
1440
3000
30
30
18
30
30
30
30
30
30
30
1
1
1
6
1
4
1
1
1
2
80
80
100
20
40
20
20
20
20
1
2400
2400
1800
3600
1200
2400
600
600
600
60
...........................................................
........................
........................
........................
21,860
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–02542 Filed 2–7–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–0260; Docket No. CDC–2020–
0008]
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:
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondent
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
SUMMARY:
VerDate Sep<11>2014
16:58 Feb 07, 2020
Jkt 250001
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 Health Hazard Evaluations/
Technical Assistance and Emerging
Problems. This proposed collection, in
accordance with mandates under the
Occupational Safety and Health Act of
1970 and the Federal Mine Safety and
Health Act of 1977, allows the National
Institute for Occupational Safety and
Health (NIOSH) to respond to requests
for HHEs to identify chemical,
biological or physical hazards in
workplaces throughout the United
States.
CDC must receive written
comments on or before April 10, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0008 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
DATES:
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
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 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,
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
E:\FR\FM\10FEN1.SGM
10FEN1
7561
Federal Register / Vol. 85, No. 27 / Monday, February 10, 2020 / Notices
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
Health Hazard Evaluations/Technical
Assistance and Emerging Problems
(OMB Control No. 0920–0260, Exp. 10/
31/2020)—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,
NIOSH responds to requests for Health
Hazard Evaluation (HHE) to identify
chemical, biological or physical hazards
in workplaces throughout the United
States. Each year, NIOSH receives
approximately 250 such requests. Most
HHE requests come from workplaces in
the following industrial sectors:
contact card may take five minutes or
less. The number of employees
monitored for workplace exposures per
on-site evaluation is estimated to be 25
per site.
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. This program entails the
mailing of follow-back questionnaires to
employer and employee representatives
at all the workplaces where NIOSH
conducted an on-site evaluation. In a
small number of instances, a followback on-site evaluation may be
completed. The first follow-back
questionnaire is sent shortly after the
first visit for an on-site evaluation and
takes about 10 minutes to complete. A
second follow-back questionnaire is sent
after the final report is completed and
requires about 20 minutes to complete.
At 12 months, a third follow-back
questionnaire is sent 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 after our response letter is
sent 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. The total
estimated burden hours is 1715. There
is no cost to respondents other than
their time.
Services, manufacturing, health and
social services, transportation, 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 website.
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). 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 25% of the requests
received, NIOSH determines an on-site
evaluation is needed.
In about 70% of on-site evaluations,
employees are interviewed in an
informal manner 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 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 notification of their exposure results.
To indicate their preference and, if
interested, provide contact information,
employees complete a contact
information post card. Completing the
jbell on DSKJLSW7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Employees and Representatives ......
VerDate Sep<11>2014
16:58 Feb 07, 2020
Number of
respondents
Form name
Health Hazard Evaluation Request
Form.
Jkt 250001
PO 00000
Frm 00036
Fmt 4703
Number of
responses per
respondent
175
Sfmt 4703
E:\FR\FM\10FEN1.SGM
1
10FEN1
Average
burden per
response
(in hrs.)
12/60
Total burden
(in hrs.)
35
7562
Federal Register / Vol. 85, No. 27 / Monday, February 10, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
Employers * .......................................
Health Hazard Evaluation Request
Form.
Health Hazard Evaluation specific
interview example.
Health Hazard Evaluation specific
questionnaire example.
Contact information post card ..........
First follow-back questionnaire ........
Employees ........................................
Employees ........................................
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 ...........................................
12/60
15
1,470
1
15/60
368
2,100
1
30/60
1,050
1,225
140
1
1
5/60
10/60
102
23
Second follow-back questionnaire ...
Third follow-back questionnaire .......
140
140
1
1
20/60
15/60
47
35
First follow-back questionnaire ........
94
1
10/60
16
Second follow-back questionnaire ...
94
1
15/60
24
...........................................................
........................
........................
........................
1,715
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2017–N–1095]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Electronic
Submission Process for Voluntary
Allegations to the Center for Devices
and Radiological Health
Food and Drug Administration,
HHS.
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
Under the Paperwork Reduction Act of
1995 (PRA), Federal Agencies are
required to publish notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on information
voluntarily submitted to the Center for
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
16:58 Feb 07, 2020
Total burden
(in hrs.)
1
[FR Doc. 2020–02541 Filed 2–7–20; 8:45 am]
ACTION:
Average
burden per
response
(in hrs.)
75
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
AGENCY:
Number of
responses per
respondent
Number of
respondents
Type of respondents
Jkt 250001
Devices and Radiological Health (CDRH)
on actual or potential health risk
concerns about a medical device or
radiological product or its use.
DATES: Submit either electronic or
written comments on the collection of
information by April 10, 2020.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before April 10,
2020. The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of April 10, 2020. Comments
received by mail/hand delivery/courier
(for written/paper submissions) will be
considered timely if they are
postmarked or the delivery service
acceptance receipt is on or before that
date.
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2017–N–1095 for ‘‘Agency Information
Collection Activities; Proposed
Collection; Comment Request;
Electronic Submission Process for
Voluntary Allegations to the Center for
Devices and Radiological Health.’’
Received comments, those filed in a
timely manner (see ADDRESSES), will be
E:\FR\FM\10FEN1.SGM
10FEN1
]]>Agencies
[Federal Register Volume 85, Number 27 (Monday, February 10, 2020)]
[Notices]
[Pages 7560-7562]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-02541]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-20-0260; Docket No. CDC-2020-0008]
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 Health Hazard Evaluations/
Technical Assistance and Emerging Problems. This proposed collection,
in accordance with mandates under the Occupational Safety and Health
Act of 1970 and the Federal Mine Safety and Health Act of 1977, allows
the National Institute for Occupational Safety and Health (NIOSH) to
respond to requests for HHEs to identify chemical, biological or
physical hazards in workplaces throughout the United States.
DATES: CDC must receive written comments on or before April 10, 2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0008 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 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, 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
[[Page 7561]]
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
Health Hazard Evaluations/Technical Assistance and Emerging
Problems (OMB Control No. 0920-0260, Exp. 10/31/2020)--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,
NIOSH responds to requests for Health Hazard Evaluation (HHE) to
identify chemical, biological or physical hazards in workplaces
throughout the United States. Each year, NIOSH receives approximately
250 such requests. Most HHE requests come from workplaces in the
following industrial sectors: Services, manufacturing, health and
social services, transportation, 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 website. 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). 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 25% of the requests received, NIOSH determines an
on-site evaluation is needed.
In about 70% of on-site evaluations, employees are interviewed in
an informal manner 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 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
notification of their exposure results. To indicate their preference
and, if interested, provide contact information, employees complete a
contact information post card. Completing the contact card may take
five minutes or less. The number of employees monitored for workplace
exposures per on-site evaluation is estimated to be 25 per site.
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. This program entails
the mailing of follow-back questionnaires to employer and employee
representatives 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
sent shortly after the first visit for an on-site evaluation and takes
about 10 minutes to complete. A second follow-back questionnaire is
sent after the final report is completed and requires about 20 minutes
to complete. At 12 months, a third follow-back questionnaire is sent
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 after our
response letter is sent 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. The total estimated burden hours is 1715. There is
no cost to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hrs.)
respondent hrs.)
----------------------------------------------------------------------------------------------------------------
Employees and Representatives. Health Hazard 175 1 12/60 35
Evaluation
Request Form.
[[Page 7562]]
Employers *................... Health Hazard 75 1 12/60 15
Evaluation
Request Form.
Employees..................... Health Hazard 1,470 1 15/60 368
Evaluation
specific
interview
example.
Employees..................... Health Hazard 2,100 1 30/60 1,050
Evaluation
specific
questionnaire
example.
Employees..................... Contact 1,225 1 5/60 102
information
post card.
Employees and Representatives; First follow- 140 1 10/60 23
Employers--Year 1 (on-site back
evaluation). questionnaire.
Second follow- 140 1 20/60 47
back
questionnaire.
Employees and Representatives; Third follow- 140 1 15/60 35
Employers--Year 2 (on-site back
evaluation). questionnaire.
Employees and Representatives; First follow- 94 1 10/60 16
Employers--Year 1 (without on- back
site evaluation). questionnaire.
Employees and Representatives; Second follow- 94 1 15/60 24
Employers--Year 2 (without on- back
site evaluation). questionnaire.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1,715
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-02541 Filed 2-7-20; 8:45 am]
BILLING CODE 4163-18-P
