Sunshine Act Notice, 3911-3912 [2020-01168]
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Federal Register / Vol. 85, No. 15 / Thursday, January 23, 2020 / Notices
docket for this ICR. The docket can be
viewed online at www.regulations.gov
or in person at the EPA Docket Center,
WJC West, Room 3334, 1301
Constitution Ave. NW, Washington, DC.
The telephone number for the Docket
Center is 202–566–1744. For additional
information about EPA’s public docket,
visit https://www.epa.gov/dockets.
Pursuant to section 3506(c)(2)(A) of
the PRA, EPA is soliciting comments
and information to enable it to: (i)
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 in completing CBI
determinations; (ii) 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;
(iii) enhance the quality, utility, and
clarity of the information to be
collected; and (iv) minimize the burden
of the collection of information on those
who are to respond, including through
the use of appropriate automated
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses. EPA will consider the
comments received and amend the ICR
as appropriate. The final ICR package
will then be submitted to OMB for
review and approval. At that time, EPA
will issue another Federal Register
notice to announce the submission of
the ICR to OMB and the opportunity to
submit additional comments to OMB.
Abstract: The U.S. Environmental
Protection Agency (EPA) established the
requirements set forth in 40 CFR, part 2,
subpart B, ‘‘Confidentiality of Business
Information.’’ The requirements govern
business confidentiality claims. The
requirements include the handling by
the Agency of business information
which is or may be entitled to
confidential treatment, requiring
business submitters to substantiate CBI
claims, determining whether such
information is entitled to confidential
treatment for reasons of business
confidentiality, and responding to
Freedom of Information Act (FOIA)
requests pursuant to 5 U.S.C. 552 for
information claimed as CBI.
Form Numbers: None.
Respondents/affected entities:
Respondents include any business
submitting information to EPA that it
claims as CBI. EPA receives such
information from both the
manufacturing (SIC codes 20–39) and
non-manufacturing sectors (no SIC
codes identified).
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Respondent’s obligation to respond:
Voluntary and mandatory.
Estimated number of respondents:
198 (total).
Frequency of response: 1 response per
respondent annually.
Total estimated burden: 752.4 hours
(per year). Burden is defined at 5 CFR
1320.03(b).
Total estimated cost: $169,290 (per
year), includes $0 annualized capital or
operation & maintenance costs.
Changes in Estimates: The revised
requests for substantiation will decrease
the estimated burden hours for each
response, although it increases the total
estimated respondent burden compared
with the ICR currently approved by
OMB. The decrease is 2 hours for each
business response; the increase is based
on an expected higher response rate
under the new form, producing an
increase from 488 hours to 752.4 hours
total. These changes are due to the
removal of a question that required a
company to describe, with specificity,
the ‘‘substantial competitive harm’’ that
would occur as a direct result of
disclosing the information. EPA
modified its substantiation questions as
a result of the U.S. Supreme Court’s
decision in Food Marketing Institute v.
Argus Leader Media (Argus), 139 S. Ct.
2356 (2019), which evaluated the
definition of ‘‘confidential’’ as used in
Exemption 4 of the Freedom of
Information Act (FOIA). 5 U.S.C.
552(b)(4). In the Argus decision, the
Court held that at least where ‘‘[1]
commercial or financial information is
both customarily and actually treated as
private by its owner and [2] provided to
the government under an assurance of
privacy, the information is ‘confidential’
within the meaning of Exemption 4.’’
Argus, 139 S. Ct. at 2366. EPA has
reduced burdens to business submitters
by removing the requirement to explain
with specificity whatever ‘‘substantial
competitive harm’’ a submitter claims
would ensue from release of each CBI
claim. The evaluation of ‘‘substantial
competitive harm’’ had required
businesses to analyze and describe the
potential impacts of release. EPA has
replaced that question with modified
questions that require a factual
description of the submitter’s handling
and treatment of the CBI-claimed
information, as well as a description of
any assurances provided by EPA at the
time of submission. This replacement
will reduce the burden on companies
since evaluation and analysis of
‘‘substantial competitive harm’’ is no
longer required. Further, EPA reframed
preexisting questions to solicit ‘‘yes’’ or
‘‘no’’ responses, which further reduces
burdens on submitters. These
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3911
modifications will result in greater
clarity to business submitters and
improved responses as the Agency
completes its confidentiality
determinations. The Agency anticipates
that this lower burden on each response
will increase the response rate from
21% in the prior analysis to 66% in the
present analysis. EPA has already
experienced an increase in response rate
as a result of the Supreme Court’s
decision and expects this change to
continue under the new form. EPA also
made other adjustments in its analysis
including adjustments in the hourly
costs for both the Agency and
responding companies as well as
removing a category of burden that was
not relevant to EPA’s information
request.
Dated: January 15, 2020.
Timothy R. Epp,
Associate General Counsel.
[FR Doc. 2020–01109 Filed 1–22–20; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL MINE SAFETY AND HEALTH
REVIEW COMMISSION
Sunshine Act Notice
10:00 a.m., Thursday,
February 13, 2020.
TIME AND DATE:
The Richard V. Backley Hearing
Room, Room 511N, 1331 Pennsylvania
Avenue NW, Washington, DC 20004
(enter from F Street entrance).
PLACE:
STATUS:
Open.
The
Commission will consider and act upon
the following in open session: Secretary
of Labor v. M-Class Mining, LLC, Docket
No. LAKE 2018–0188–R. (Issues include
whether the Judge erred in ruling that a
section 103(k) safety order was validly
issued and was not an abuse of
discretion.)
Any person attending this meeting
who requires special accessibility
features and/or auxiliary aids, such as
sign language interpreters, must inform
the Commission in advance of those
needs. Subject to 29 CFR 2706.150(a)(3)
and 2706.160(d).
MATTERS TO BE CONSIDERED:
CONTACT PERSON FOR MORE INFORMATION:
Emogene Johnson (202) 434–9935/(202)
708–9300 for TDD Relay/1–800–877–
8339 for toll free.
Phone Number for Listening to
Meeting: 1 (866) 236–7472.
Passcode: 678–100.
Authority: 5 U.S.C. 552b.
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3912
Federal Register / Vol. 85, No. 15 / Thursday, January 23, 2020 / Notices
Dated: January 21, 2020.
Sarah L. Stewart,
Deputy General Counsel.
[FR Doc. 2020–01168 Filed 1–21–20; 4:15 pm]
BILLING CODE 6735–01–P
GENERAL SERVICES
ADMINISTRATION
[Notice–QQE–2020–01; Docket No. 2020–
0002; Sequence No. 1]
Publication of Website Standards
Technology Transformation
Services (TTS), Federal Acquisition
Service (FAS), General Services
Administration (GSA).
ACTION: Notice.
AGENCY:
The 21st Century Integrated
Digital Experience Act requires any
public website of an executive agency to
comply with GSA’s website standards.
GSA publishes the standards at https://
designsystem.digital.gov/websitestandards. To notify agencies of
revisions to the website standards, GSA
will periodically update the U.S. Web
Design System website and publish
notices in the Federal Register.
DATES: The website standards were first
published on January 22, 2020. They
were last revised on January 22, 2020.
FOR FURTHER INFORMATION CONTACT: For
clarification of content, contact Mr.
Jacob Parcell, Director, Innovation
Portfolio, Technology Transformation
Services, at 202–208–7139, or by email
at uswds@support.digitalgov.gov.
Please cite Notice of website
Standards.
SUMMARY:
Dated: January 16, 2020.
Anil Cheriyan,
Deputy Commissioner, Federal Acquisition
Service and Director, Technology
Transformation Services.
[FR Doc. 2020–01068 Filed 1–22–20; 8:45 am]
BILLING CODE 4733–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–19AYV]
Proposed Project
jbell on DSKJLSW7X2PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Public Health
Laboratory Testing for Emerging
VerDate Sep<11>2014
17:13 Jan 22, 2020
Antibiotic Resistance and Fungal
Threats to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on July 5th,
2019 to obtain comments from the
public and affected agencies. CDC
received one comment from the public.
This notice serves to allow an additional
30 days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, 725 17th Street NW,
Washington, DC 20503 or by fax to (202)
395–5806. Provide written comments
within 30 days of notice publication.
Jkt 250001
Public Health Laboratory Testing for
Emerging Antibiotic Resistance and
Fungal Threats—Existing Collection in
Use without an OMB Control Number—
National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
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Background and Brief Description
This state and local laboratory testing
capacity study is being implemented by
the Department of Health and Human
Services (HHS), Centers for Disease
Control and Prevention (CDC) in
response to the Executive Order 13676
of September 18, 2014, the National
Strategy of September 2014 and to
implement sub-objective 2.1.1 of the
National Action Plan of March 2015 for
Combating Antibiotic Resistant Bacteria.
Data collected throughout this network
is also authorized by Section 301 of the
Public Health Service Act (42 U.S.C.
241).
The Antibiotic Resistance Laboratory
Network (AR Lab Network) is made up
of jurisdictional public health
laboratories (i.e. all fifty states, four
large cities, and Puerto Rico). These
public health laboratories will be
equipped to detect and characterize
isolates of carbapenem-resistant
Enterobacteriaceae (CRE), carbapenemresistant Pseudomonas aeruginosa
(CRPA), and carbapenem-resistant
Acinetobacter baumannii (CRAB), as
well as carbapenemase-positive
organisms (CPOs) from colonization
screening swabs. These resistant
bacteria are becoming more and more
prevalent, particularly in healthcare
settings, and are typically identified in
clinical laboratories, but
characterization is often limited. The
laboratory testing will allow for
additional testing and characterization,
including use of gold-standard methods.
Isolate characterization includes
organism identification, antimicrobial
susceptibility testing (AST) to confirm
carbapenem resistance and determine
susceptibility to new drugs of
therapeutic and epidemiological
importance, a phenotypic method to
detect carbapenemase enzyme
production, and molecular testing to
identify the resistance mechanism(s).
Screening swabs will undergo molecular
testing to identify whether
carbapenemase-producing organisms are
present.
Results from this laboratory testing
will be used to (1) identify targets for
infection control, (2) detect new types of
resistance, (3) characterize geographical
distribution of resistance, (4) determine
whether resistance mechanisms are
spreading among organisms, people,
and facilities, and (5) provide data that
informs state and local public health
surveillance and prevention activities
and priorities. Additionally, some
jurisdictions will participate in
reference identification of Candida spp.
to aid in these pursuits using matrixassisted laser desorption ionization/
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Agencies
[Federal Register Volume 85, Number 15 (Thursday, January 23, 2020)]
[Notices]
[Pages 3911-3912]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01168]
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FEDERAL MINE SAFETY AND HEALTH REVIEW COMMISSION
Sunshine Act Notice
TIME AND DATE: 10:00 a.m., Thursday, February 13, 2020.
PLACE: The Richard V. Backley Hearing Room, Room 511N, 1331
Pennsylvania Avenue NW, Washington, DC 20004 (enter from F Street
entrance).
STATUS: Open.
MATTERS TO BE CONSIDERED: The Commission will consider and act upon the
following in open session: Secretary of Labor v. M-Class Mining, LLC,
Docket No. LAKE 2018-0188-R. (Issues include whether the Judge erred in
ruling that a section 103(k) safety order was validly issued and was
not an abuse of discretion.)
Any person attending this meeting who requires special
accessibility features and/or auxiliary aids, such as sign language
interpreters, must inform the Commission in advance of those needs.
Subject to 29 CFR 2706.150(a)(3) and 2706.160(d).
CONTACT PERSON FOR MORE INFORMATION: Emogene Johnson (202) 434-9935/
(202) 708-9300 for TDD Relay/1-800-877-8339 for toll free.
Phone Number for Listening to Meeting: 1 (866) 236-7472.
Passcode: 678-100.
Authority: 5 U.S.C. 552b.
[[Page 3912]]
Dated: January 21, 2020.
Sarah L. Stewart,
Deputy General Counsel.
[FR Doc. 2020-01168 Filed 1-21-20; 4:15 pm]
BILLING CODE 6735-01-P