Advisory Committee on Immunization Practices; Cancellation of Meeting, 73558-73559 [2022-26084]
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Federal Register / Vol. 87, No. 229 / Wednesday, November 30, 2022 / Notices
currently approved through May 31,
2023. An Agency may not conduct or
sponsor and a person is not required to
respond to a collection of information
unless it displays a currently valid OMB
control number.
DATES: Comments must be submitted on
or before January 30, 2023.
ADDRESSES: Submit your comments,
referencing Docket ID No. EPA–HQ–
OECA–2013–0547, online using
www.regulations.gov (our preferred
method), by email to docket.oeca@
epa.gov, or by mail to: EPA Docket
Center, Environmental Protection
Agency, Mail Code 28221T, 1200
Pennsylvania Ave. NW, Washington, DC
20460.
EPA’s policy is that all comments
received will be included in the public
docket without change including any
personal information provided, unless
the comment includes profanity, threats,
information claimed to be Confidential
Business Information (CBI) or other
information whose disclosure is
restricted by statute.
FOR FURTHER INFORMATION CONTACT:
Gregory Savitske, Monitoring,
Assistance, and Media Programs
Division, Office of Compliance, (2227A),
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460; telephone number: (202) 564–
2601; fax number: (202) 564–0050;
email address: Savitske.Gregory@
epa.gov.
SUPPLEMENTARY INFORMATION:
Supporting documents which explain in
detail the information that the EPA will
be collecting are available in the public
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 Paperwork Reduction Act, 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; (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
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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: Discharge Monitoring
Report-Quality Assurance (DMR–QA)
study program participation is
mandatory for Major and selected Minor
National Pollutant Discharge
Elimination System (NPDES) permit
holders in accordance with Clean Water
Act Section 308. The DMR–QA study
program is designed to evaluate the
analytic ability of laboratories that
perform chemical, microbiological and
whole effluent toxicity (WET) analyses
required in NPDES permits for reporting
results in the Discharge Monitoring
Reports (DMR). Under DMR–QA, the
permit holder is responsible for having
their in-house and/or contract
laboratories analyze proficiency test
samples and submit results to
proficiency testing (PT) providers for
grading. Graded results are transmitted
by either the permit holder or PT
provider to the appropriate federal or
state NPDES permitting authority.
Permit holders are responsible for
submitting corrective action reports to
the appropriate permitting authority.
Form Numbers: 6400–01.
Respondents/affected entities: Major
and selected Minor permit holders
under the Clean Water Act’s National
Pollutant Discharge Elimination System
(NPDES).
Respondent’s obligation to respond:
Major permit holders must participate
annually. Minor permit holders must
participate if selected by the state or
EPA DMR–QA coordinator.
Estimated number of respondents:
5,500 (total).
Frequency of response: Major permit
holders must participate annually.
Minor permit holders must participate if
selected by the state or EPA DMR–QA
coordinator.
Total estimated burden: 36,300 hours
(per year). Burden is defined at 5 CFR
1320.03(b).
Total estimated cost: $5,240,070 (per
year), includes $3,243,350 annualized
capital or operation & maintenance
costs.
Changes in estimates: The total
estimated respondent burden is
projected to remain the same as the ICR
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currently approved by OMB; this is
attributed to the estimated number of
respondents receiving this ICR
remaining stable over the past three
years. Labor costs will likely increase to
account for changes in employee benefit
and compensation costs as well as
inflation. Non-labor costs for obtaining
proficiency test samples will also likely
increase.
Dated: November 23, 2022.
Elizabeth Vizard,
Acting Director, Monitoring, Assistance, and
Media Programs Division, Office of
Compliance.
[FR Doc. 2022–26087 Filed 11–29–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2022–0136]
Advisory Committee on Immunization
Practices; Cancellation of Meeting
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
ACTION:
Notice.
Notice is
hereby given of a change in the meeting
of the Advisory Committee on
Immunization Practices (ACIP);
December 9, 2022, from 10 a.m. to 5
p.m., EST. The virtual meeting was
published in the Federal Register on
November 23, 2022, Volume 87,
Number 225, pages 71641–71642. This
meeting is being canceled in its entirety.
SUPPLEMENTARY INFORMATION:
FOR FURTHER INFORMATION CONTACT:
Stephanie Thomas, ACIP Committee
Management Specialist, Centers for
Disease Control and Prevention,
National Center for Immunization and
Respiratory Diseases, 1600 Clifton Road
NE, Mailstop H24–8, Atlanta, Georgia
30329–4027; Telephone: 404–639–8836;
Email: ACIP@cdc.gov.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
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Federal Register / Vol. 87, No. 229 / Wednesday, November 30, 2022 / Notices
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2022–26084 Filed 11–29–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
[OMB Control No. 0985–0029]
Agency Information Collection
Activities: Proposed Collection; Public
Comment Request of the State
Councils on Developmental Disabilities
(Councils) State Plan
Administration for Community
Living, Department of Health and
Human Services.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) is announcing
an opportunity for the public to
comment on the proposed collection of
information listed above. Under the
Paperwork Reduction Act of 1995
(PRA), Federal agencies are required to
publish a 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 Information Collection (IC)
Revision solicits comments on the
information collection requirements
relating to the Developmental
Disabilities State Plan OMB control
number 0985–0029.
DATES: Comments on the collection of
information must be submitted
electronically by 11:59 p.m. (EST) or
postmarked by January 30, 2023.
ADDRESSES: Submit comments on the
collection of information via email to
Sara.Newell-Perez@acl.hhs.gov or to
Administration for Community Living,
330 C Street SW, Washington, DC
20201, Attention: Sara Newell-Perez.
FOR FURTHER INFORMATION CONTACT: Sara
Newell-Perez, 202–795–7413 or
Sara.Newell-Perez@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
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.
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SUMMARY:
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‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
The PRA requires Federal agencies to
provide a 60-day notice in the Federal
Register concerning each proposed
collection of information, including
each proposed extension of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, ACL is publishing a notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, ACL invites
comments on our burden estimates or
any other aspect of this collection of
information, including:
(1) whether the proposed collection of
information is necessary for the proper
performance of ACL’s functions,
including whether the information will
have practical utility;
(2) the accuracy of ACL’s estimate of
the burden of the proposed collection of
information, including the validity of
the methodology and assumptions used
to determine burden estimates;
(3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and
(4) ways to minimize the burden of
the collection of information on
respondents, including through the use
of automated collection techniques
when appropriate, and other forms of
information technology.
The State Councils on Developmental
Disabilities (Councils) are authorized in
Subtitle B, of the Developmental
Disabilities Assistance and Bill of Rights
Act of 2000 (DD Act), as amended, [42
U.S.C. 15001 et seq.] (The DD Act). The
DD Act requires Councils to submit a
five-year State plan. Section 124(a) [42
U.S.C. 15024(a)], states that: Any State
desiring to receive assistance under this
subtitle shall submit to the Secretary,
and obtain approval of, a 5-year
strategic State plan under this section.
The DD Act regulations outlines
additional guiding requirements in 45
CFR part 1326.30(a), which states that:
In order to receive Federal financial
assistance under this subpart, each
State Developmental Disabilities
Council must prepare and submit to the
Secretary, and have in effect, a State
plan which meets the requirements of
sections 122 and 124 of the Act (42
U.S.C. 6022 and 6024) and these
regulations.
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73559
The Council is responsible for the
development, and submission of the
State plan as well as implementation of
the activities described in the plan. The
Council updates the Sate plan annually
during the five years. The State plan
provides information on individuals
with developmental disabilities in the
State, and a description of the services
available to them and their families. The
State plan sets forth the goals and
specific objectives to be achieved by the
State Council in pursuing systems
change and capacity building that result
in empowering people with
developmental disabilities to lead
independent lives within the
community. It describes State priorities,
strategies, and actions, and the
allocation of funds to meet these goals
and objectives. Additionally, the data
collected in the State plan and
submitted to ACL is also used to comply
with the GPRA Modernization Act of
2010 (GPRAMA).
The State Plan is used in three ways.
First, it provides a framework for
citizens, State governments, and other
key stakeholder to provide input and
comments to help shape the goals and
objectives during the development
stage. Secondly, it is used by each
Council as a planning document to
operationalize its goals and strategies.
Finally, it provides information the
Department needs for monitoring and
providing technical assistance to ensure
the Council is compliant.
This is a revision of a currently
approved information collect that
expires March 30, 2023. To ensure the
DD Council State plan is consistent with
the Executive Order on Advancing
Racial Equity and Support for
Underserved Communities Through the
Federal Government and the Executive
Order on Advancing Equality for
Lesbian, Gay, Bisexual, Transgender,
Queer, and Intersex Individuals, ACL
intends to determine whether sexual
orientation and gender identity (SOGI)
data elements need to be adapted prior
to adding them to ensure accessibility of
the questions for individuals with
intellectual and developmental
disabilities.
The proposed data collection tool may
be found on the ACL website for review
at: https://www.acl.gov/about-acl/
public-input.
Estimated Program Burden: ACL
estimates the burden of this collection
of information as follows:
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]]>Agencies
[Federal Register Volume 87, Number 229 (Wednesday, November 30, 2022)]
[Notices]
[Pages 73558-73559]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-26084]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[Docket No. CDC-2022-0136]
Advisory Committee on Immunization Practices; Cancellation of
Meeting
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUPPLEMENTARY INFORMATION: Notice is hereby given of a change in the
meeting of the Advisory Committee on Immunization Practices (ACIP);
December 9, 2022, from 10 a.m. to 5 p.m., EST. The virtual meeting was
published in the Federal Register on November 23, 2022, Volume 87,
Number 225, pages 71641-71642. This meeting is being canceled in its
entirety.
FOR FURTHER INFORMATION CONTACT: Stephanie Thomas, ACIP Committee
Management Specialist, Centers for Disease Control and Prevention,
National Center for Immunization and Respiratory Diseases, 1600 Clifton
Road NE, Mailstop H24-8, Atlanta, Georgia 30329-4027; Telephone: 404-
639-8836; Email: [email protected].
The Director, Strategic Business Initiatives Unit, Office of the
Chief Operating Officer, Centers for Disease Control and Prevention,
has been delegated the authority to sign Federal Register notices
pertaining to announcements of meetings and other committee management
activities, for both the Centers for Disease Control and
[[Page 73559]]
Prevention and the Agency for Toxic Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease Control and Prevention.
[FR Doc. 2022-26084 Filed 11-29-22; 8:45 am]
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