Availability of Draft Toxicological Profiles, 66898-66899 [2019-26361]
Download as PDF
66898
Federal Register / Vol. 84, No. 235 / Friday, December 6, 2019 / Notices
Open Session
FEDERAL RESERVE SYSTEM
Change in Bank Control Notices;
Acquisitions of Shares of a Bank or
Bank Holding Company
The notificants listed below have
applied under the Change in Bank
Control Act (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 applications listed below, as well
as other related filings required by the
Board, if any, are available for
immediate inspection at the Federal
Reserve Bank indicated. The
applications will also be available for
inspection at the offices of the Board of
Governors. Interested persons may
express their views in writing on the
standards enumerated in paragraph 7 of
the Act.
Comments regarding each of these
applications must be received at the
Reserve Bank indicated or the offices of
the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th
Street and Constitution Avenue NW,
Washington DC 20551–0001, not later
than December 23, 2019.
A. Federal Reserve Bank of St. Louis
(David L. Hubbard, Senior Manager)
P.O. Box 442, St. Louis, Missouri
63166–2034. Comments can also be sent
electronically to
Comments.applications@stls.frb.org:
1. Kalista Ann Stover Carroll, Dyer,
Tennessee, and Terrie Lou Stover
Joyner, Trenton, Tennessee;
individually, and as members of a group
acting in concert with Julie Joyner
Hager, Trenton, Tennessee, and Kellie
Joyner Ashburn, Rives, Tennessee, to
retain voting shares of Dyer F & M
Bancshares, Inc., and thereby indirectly
retain voting shares of The Farmers &
Merchants Bank, both of Dyer,
Tennessee.
Board of Governors of the Federal Reserve
System, December 3, 2019.
Yao-Chin Chao,
Assistant Secretary of the Board.
[FR Doc. 2019–26382 Filed 12–5–19; 8:45 am]
lotter on DSKBCFDHB2PROD with NOTICES
BILLING CODE P
FEDERAL RETIREMENT THRIFT
INVESTMENT
Board Member Meeting
77 K Street NE, 10th Floor, Washington,
DC 20002
December 16, 2019, 10:00 a.m.,
Telephonic
VerDate Sep<11>2014
16:11 Dec 05, 2019
Jkt 250001
1. Approval of the November 13, 2019
Board Meeting Minutes
2. Monthly Reports
(a) Participant Activity Report
(b) Investment Performance
(c) Legislative Report
3. Quarterly Reports
(d) Vendor Risk Management Update
Closed Session
Information covered under 5 U.S.C.
552b (c)(4).
FOR FURTHER INFORMATION CONTACT:
Kimberly Weaver, Director, Office of
External Affairs, (202) 942–1640.
Dated: December 3, 2019.
Megan Grumbine,
General Counsel, Federal Retirement Thrift
Investment Board.
[FR Doc. 2019–26376 Filed 12–5–19; 8:45 am]
BILLING CODE 6760–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Toxic Substances and
Disease Registry
[Docket No. ATSDR–2019–0008]
Availability of Draft Toxicological
Profiles
Agency for Toxic Substances
and Disease Registry (ATSDR),
Department of Health and Human
Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Agency for Toxic
Substances and Disease Registry
(ATSDR), within the Department of
Health and Human Services (HHS),
announces the opening of a docket to
obtain comments on Draft Toxicological
Profiles for 1,2-Dichloropropane, 1,1Dichloroethene, Di(2ethylhexyl)phthalate (DEHP), DDT/
DDE/DDD, Chlorobenzene,
Hexachlorobutadiene, and 1,1,2Trichloroethane.
SUMMARY:
Written comments must be
received on or before March 5, 2020.
ADDRESSES: You may submit comments,
identified by docket number ATSDR–
2019–0008, by any of the following
methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Division of Toxicology and
Human Health Sciences, Agency for
Toxic Substances and Disease Registry,
1600 Clifton Rd. NE, Mail Stop S102–1,
Atlanta, GA 30329–4027. Attn: Docket
No. ATSDR–201x–0008.
DATES:
PO 00000
Frm 00029
Fmt 4703
Sfmt 4703
Instructions: All submissions must
include the agency name and Docket
Number. All relevant comments
received will be posted without change
to https://regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
https://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Susan Ingber, Agency for Toxic
Substances and Disease Registry,
Division of Toxicology and Human
Health Sciences, 1600 Clifton Rd. NE,
Mail Stop S102–1, Atlanta, GA 30329–
4027, Email: ATSDRToxProfileFRNs@
cdc.gov; Phone: 1–800–232–4636.
SUPPLEMENTARY INFORMATION: ATSDR
has updated these profiles based on
availability of new health effects
information since their initial release.
On March 21, 2016 ATSDR announced
that it was preparing to develop Draft
Toxicological Profiles for public
comment release (81 FR 15110), which
include those profiles mentioned above.
All toxicological profiles issued as
‘‘Drafts for Public Comment’’ represent
the result of ATSDR’s evidence-based
evaluations to provide important
toxicological information on priority
hazardous substances. ATSDR is
seeking public comments and additional
information or reports on studies about
the health effects of 1,2dichloropropane, 1,1-dichloroethene,
di(2-ethylhexyl)phthalate (DEHP), DDT,
DDE, DDD, chlorobenzene,
hexachlorobutadiene, and 1,1,2trichloroethane for review and potential
inclusion in the profiles. ATSDR
considers key studies for these
substances during the profile
development process. This document
solicits any relevant, additional studies.
ATSDR will evaluate the quality and
relevance of such data or studies for
possible inclusion into the profile.
Public Participation
Interested persons or organizations
are invited to participate by submitting
written views, information, and data.
Please note that comments received,
including attachments and other
supporting materials, are part of the
public record and are subject to public
disclosure. Comments will be posted on
https://www.regulations.gov. Therefore,
do not include any information in your
comment or supporting materials that
you consider confidential or
inappropriate for public disclosure. If
you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be on
public display. ATSDR will review all
E:\FR\FM\06DEN1.SGM
06DEN1
Federal Register / Vol. 84, No. 235 / Friday, December 6, 2019 / Notices
submissions and may choose to redact,
or withhold, submissions containing
private or proprietary information such
as Social Security numbers, medical
information, inappropriate language, or
duplicate/near duplicate examples of a
mass-mail campaign. ATSDR will
carefully consider all comments
submitted in preparation of the final
Toxicological Profiles and may revise
the profiles as appropriate.
The Superfund Amendments and
Reauthorization Act of 1986 (SARA) [42
U.S.C. 9601 et seq.] amended the
Comprehensive Environmental
Response, Compensation, and Liability
Act of 1980 (CERCLA or Superfund) [42
U.S.C. 9601 et seq.] by establishing
certain requirements for ATSDR and the
U.S. Environmental Protection Agency
(EPA) regarding the hazardous
substances most commonly found at
facilities on the CERCLA National
Priorities List (NPL). Among these
statutory requirements is a mandate for
the Administrator of ATSDR to prepare
toxicological profiles for each substance
included on the priority list of
hazardous substances [also called the
Substance Priority List (SPL)]. This list
identifies 275 hazardous substances that
ATSDR and EPA have determined pose
the most significant potential threat to
human health. The SPL is available
online at www.atsdr.cdc.gov/spl.
In addition, CERCLA provides ATSDR
with the authority to prepare
toxicological profiles for substances not
found on the SPL. CERCLA authorizes
ATSDR to establish and maintain an
inventory of literature, research, and
studies on the health effects of toxic
substances (CERCLA Section
104(i)(1)(B); 42 U.S.C. 9604(i)(1)(B)); to
respond to requests for health
consultations (CERCLA Section
104(i)(4); 42 U.S.C. 9604(i)(4)); and to
support the site-specific response
actions conducted by the agency.
Availability
lotter on DSKBCFDHB2PROD with NOTICES
These Draft Toxicological Profiles will
be available online at https://
www.atsdr.cdc.gov/ToxProfiles and at
www.regulations.gov, Docket No.
ATSDR–0008.
Pamela I. Protzel Berman,
Director, Office of Policy, Partnerships and
Planning, Agency for Toxic Substances and
Disease Registry.
[FR Doc. 2019–26361 Filed 12–5–19; 8:45 am]
BILLING CODE 4163–70–P
16:11 Dec 05, 2019
Centers for Disease Control and
Prevention
[60Day–20–0263; Docket No. CDC–2019–
0110]
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:
Legislative Background
VerDate Sep<11>2014
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Jkt 250001
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
Requirements for the Importation of
Nonhuman Primates into the United
States. This information collection
contains the reporting and
documentation requirements for
registered importers of nonhuman
primates, as outlined in 42 Code of
Federal Regulations part 71.53
Requirements for importers of
nonhuman primates.
DATES: CDC must receive written
comments on or before February 4,
2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0110 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 comments 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 Jeffrey M. Zirger, of
the Information Collection Review
Office, Centers for Disease Control and
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
66899
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.
Proposed Project
Requirements for the Importation of
Nonhuman Primates into the United
States (OMB Control No. 0920–0263,
Exp. 08/31/2020)—Revision—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
Under the 42 CFR 71.53, CDC collects
information pertaining to importers and
imported nonhuman primates. This
information collection enables CDC to
evaluate compliance with pre-arrival of
shipment notification requirements, to
investigate the number and species of
imported nonhuman primates, and to
E:\FR\FM\06DEN1.SGM
06DEN1
Agencies
[Federal Register Volume 84, Number 235 (Friday, December 6, 2019)]
[Notices]
[Pages 66898-66899]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-26361]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Toxic Substances and Disease Registry
[Docket No. ATSDR-2019-0008]
Availability of Draft Toxicological Profiles
AGENCY: Agency for Toxic Substances and Disease Registry (ATSDR),
Department of Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Agency for Toxic Substances and Disease Registry (ATSDR),
within the Department of Health and Human Services (HHS), announces the
opening of a docket to obtain comments on Draft Toxicological Profiles
for 1,2-Dichloropropane, 1,1-Dichloroethene, Di(2-ethylhexyl)phthalate
(DEHP), DDT/DDE/DDD, Chlorobenzene, Hexachlorobutadiene, and 1,1,2-
Trichloroethane.
DATES: Written comments must be received on or before March 5, 2020.
ADDRESSES: You may submit comments, identified by docket number ATSDR-
2019-0008, by any of the following methods:
Federal eRulemaking Portal: www.regulations.gov. Follow
the instructions for submitting comments.
Mail: Division of Toxicology and Human Health Sciences,
Agency for Toxic Substances and Disease Registry, 1600 Clifton Rd. NE,
Mail Stop S102-1, Atlanta, GA 30329-4027. Attn: Docket No. ATSDR-201x-
0008.
Instructions: All submissions must include the agency name and
Docket Number. All relevant comments received will be posted without
change to https://regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to https://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT: Susan Ingber, Agency for Toxic
Substances and Disease Registry, Division of Toxicology and Human
Health Sciences, 1600 Clifton Rd. NE, Mail Stop S102-1, Atlanta, GA
30329-4027, Email: [email protected]; Phone: 1-800-232-4636.
SUPPLEMENTARY INFORMATION: ATSDR has updated these profiles based on
availability of new health effects information since their initial
release. On March 21, 2016 ATSDR announced that it was preparing to
develop Draft Toxicological Profiles for public comment release (81 FR
15110), which include those profiles mentioned above. All toxicological
profiles issued as ``Drafts for Public Comment'' represent the result
of ATSDR's evidence-based evaluations to provide important
toxicological information on priority hazardous substances. ATSDR is
seeking public comments and additional information or reports on
studies about the health effects of 1,2-dichloropropane, 1,1-
dichloroethene, di(2-ethylhexyl)phthalate (DEHP), DDT, DDE, DDD,
chlorobenzene, hexachlorobutadiene, and 1,1,2-trichloroethane for
review and potential inclusion in the profiles. ATSDR considers key
studies for these substances during the profile development process.
This document solicits any relevant, additional studies. ATSDR will
evaluate the quality and relevance of such data or studies for possible
inclusion into the profile.
Public Participation
Interested persons or organizations are invited to participate by
submitting written views, information, and data.
Please note that comments received, including attachments and other
supporting materials, are part of the public record and are subject to
public disclosure. Comments will be posted on https://www.regulations.gov. Therefore, do not include any information in your
comment or supporting materials that you consider confidential or
inappropriate for public disclosure. If you include your name, contact
information, or other information that identifies you in the body of
your comments, that information will be on public display. ATSDR will
review all
[[Page 66899]]
submissions and may choose to redact, or withhold, submissions
containing private or proprietary information such as Social Security
numbers, medical information, inappropriate language, or duplicate/near
duplicate examples of a mass-mail campaign. ATSDR will carefully
consider all comments submitted in preparation of the final
Toxicological Profiles and may revise the profiles as appropriate.
Legislative Background
The Superfund Amendments and Reauthorization Act of 1986 (SARA) [42
U.S.C. 9601 et seq.] amended the Comprehensive Environmental Response,
Compensation, and Liability Act of 1980 (CERCLA or Superfund) [42
U.S.C. 9601 et seq.] by establishing certain requirements for ATSDR and
the U.S. Environmental Protection Agency (EPA) regarding the hazardous
substances most commonly found at facilities on the CERCLA National
Priorities List (NPL). Among these statutory requirements is a mandate
for the Administrator of ATSDR to prepare toxicological profiles for
each substance included on the priority list of hazardous substances
[also called the Substance Priority List (SPL)]. This list identifies
275 hazardous substances that ATSDR and EPA have determined pose the
most significant potential threat to human health. The SPL is available
online at www.atsdr.cdc.gov/spl.
In addition, CERCLA provides ATSDR with the authority to prepare
toxicological profiles for substances not found on the SPL. CERCLA
authorizes ATSDR to establish and maintain an inventory of literature,
research, and studies on the health effects of toxic substances (CERCLA
Section 104(i)(1)(B); 42 U.S.C. 9604(i)(1)(B)); to respond to requests
for health consultations (CERCLA Section 104(i)(4); 42 U.S.C.
9604(i)(4)); and to support the site-specific response actions
conducted by the agency.
Availability
These Draft Toxicological Profiles will be available online at
https://www.atsdr.cdc.gov/ToxProfiles and at www.regulations.gov, Docket
No. ATSDR-0008.
Pamela I. Protzel Berman,
Director, Office of Policy, Partnerships and Planning, Agency for Toxic
Substances and Disease Registry.
[FR Doc. 2019-26361 Filed 12-5-19; 8:45 am]
BILLING CODE 4163-70-P