Sunshine Act Meeting, 9267 [2015-03605]
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Federal Register / Vol. 80, No. 34 / Friday, February 20, 2015 / Notices
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Document Status should be Final EIS.
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9922–98–Region 6]
Underground Injection Control
Program; Hazardous Waste Injection
Restrictions; Petition for Exemption
Reissuance—Class I Hazardous Waste
Injection; Lucite International, Inc.
Beaumont Site, Nederland, TX
Jkt 235001
BILLING CODE 6714–01–P
Dated: February 5, 2015.
William K. Honker,
Director, Water Quality Protection Division.
Investigating and Reporting Adverse
Reactions Related to Human Cells,
Tissues, and Cellular and TissueBased Products; Draft Guidance for
Industry; Availability
AGENCY:
[FR Doc. 2015–03463 Filed 2–19–15; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2015–D–0349]
Food and Drug Administration,
HHS.
ACTION:
Notice.
BILLING CODE 6560–50–P
The Food and Drug
Administration (FDA) is announcing the
availability of a draft document entitled
‘‘Investigating and Reporting Adverse
Reactions Related to Human Cells,
Tissues, and Cellular and Tissue-Based
Products (HCT/Ps) Regulated Solely
Under Section 361 of the Public Health
Service Act and 21 CFR part 1271’’
dated February 2015. The draft guidance
document is intended to provide
manufacturers of human cells, tissues,
and cellular and tissue-based products
(HCT/Ps) for which no premarket
submissions are required because they
are not also regulated as drugs, devices,
and/or biological products, with
recommendations for complying with
the requirements for investigating and
reporting adverse reactions involving
communicable disease in recipients of
these HCT/Ps. The draft guidance, when
finalized, is intended to supplement
section XXII of FDA’s guidance entitled
‘‘Guidance for Industry: Current Good
Tissue Practice (CGTP) and Additional
Requirements for Manufacturers of
Human Cells, Tissues, and Cellular and
Tissue-Based Products (HCT/Ps)’’ dated
December 2011 and supersede the
guidance entitled ‘‘Guidance for
Industry: MedWatch Form FDA 3500A:
Mandatory Reporting of Adverse
Reactions Related to Human Cells,
Tissues, and Cellular and Tissue-Based
Products (HCT/Ps)’’ dated November
2005.
SUMMARY:
Sunshine Act Meeting
Notice is hereby given that a
reissuance of an exemption to the land
disposal Restrictions, under the 1984
Hazardous and Solid Waste
Amendments to the Resource
Conservation and Recovery Act, has
been granted to Lucite International,
Inc. for two Class I hazardous injection
wells located at their Beaumont site
located in Nederland, TX. The company
has adequately demonstrated to the
satisfaction of the Environmental
Protection Agency by the petition
reissuance application and supporting
documentation that, to a reasonable
degree of certainty, there will be no
migration of hazardous constituents
from the injection zone for as long as the
waste remains hazardous. This final
decision allows the continued
underground injection by Lucite, of the
specific restricted hazardous wastes
identified in this exemption reissuance,
into Class I hazardous waste injection
wells WDW–100 & 101 until December
31, 2030, unless EPA moves to
terminate this exemption. Additional
conditions included in this final
decision may be reviewed by contacting
the Region 6 Ground Water/UIC Section.
A public notice was issued December
18, 2014. The public comment period
closed on February 2, 2015. No
comments were received. This decision
constitutes final Agency action and
there is no Administrative appeal. This
decision may be reviewed/appealed in
SUMMARY:
Copies of the petition
reissuance and all pertinent information
relating thereto are on file at the
following location: Environmental
Protection Agency, Region 6, Water
Quality Protection Division, Source
Water Protection Branch (6WQ–S), 1445
Ross Avenue, Dallas, Texas 75202–2733.
ADDRESSES:
FEDERAL DEPOSIT INSURANCE
CORPORATION
Environmental Protection
Agency (EPA).
ACTION: Notice of a final decision on a
no migration petition reissuance.
AGENCY:
TKELLEY on DSK3SPTVN1PROD with NOTICES
[FR Doc. 2015–03605 Filed 2–18–15; 4:15 pm]
Philip Dellinger, Chief Ground Water/
UIC Section, EPA—Region 6, telephone
(214) 665–8324.
[FR Doc. 2015–03524 Filed 2–19–15; 8:45 am]
17:07 Feb 19, 2015
This action is effective as of
February 5, 2015.
DATES:
Federal Deposit Insurance Corporation.
Robert E. Feldman,
Executive Secretary.
FOR FURTHER INFORMATION CONTACT:
Dated: February 17, 2015.
Dawn Roberts,
Management Analyst, NEPA Compliance
Division, Office of Federal Activities.
VerDate Sep<11>2014
compliance with the Administrative
Procedure Act.
9267
Pursuant to the provisions of the
‘‘Government in the Sunshine Act’’ (5
U.S.C. 552b), notice is hereby given that
at 10:03 a.m. on Tuesday, February 17,
2015, the Board of Directors of the
Federal Deposit Insurance Corporation
met in closed session to consider
matters related to the Corporation’s
supervision, corporate, and resolution
activities.
In calling the meeting, the Board
determined, on motion of Vice
Chairman Thomas M. Hoenig, seconded
by Director Jeremiah O. Norton
(Appointive), concurred in by Director
Thomas J. Curry (Comptroller of the
Currency), Director Richard Cordray
(Director, Consumer Financial
Protection Bureau), and Chairman
Martin J. Gruenberg, that Corporation
business required its consideration of
the matters which were to be the subject
of this meeting on less than seven days’
notice to the public; that no earlier
notice of the meeting was practicable;
that the public interest did not require
consideration of the matters in a
meeting open to public observation; and
that the matters could be considered in
a closed meeting by authority of
subsections (c)(4), (c)(6), (c)(8),
(c)(9)(A)(ii), and (c)(9)(B) of the
‘‘Government in the Sunshine Act’’ (5
U.S.C. 552b(c)(4), (c)(6), (c)(8),
(c)(9)(A)(ii), and (c)(9)(B).
The meeting was held by telephone.
Dated: February 17, 2015.
PO 00000
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Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the Agency
considers your comment on this draft
guidance before it begins work on the
final version of the guidance, submit
either electronic or written comments
on the draft guidance by April 21, 2015.
DATES:
E:\FR\FM\20FEN1.SGM
20FEN1
Agencies
[Federal Register Volume 80, Number 34 (Friday, February 20, 2015)]
[Notices]
[Page 9267]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-03605]
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FEDERAL DEPOSIT INSURANCE CORPORATION
Sunshine Act Meeting
Pursuant to the provisions of the ``Government in the Sunshine
Act'' (5 U.S.C. 552b), notice is hereby given that at 10:03 a.m. on
Tuesday, February 17, 2015, the Board of Directors of the Federal
Deposit Insurance Corporation met in closed session to consider matters
related to the Corporation's supervision, corporate, and resolution
activities.
In calling the meeting, the Board determined, on motion of Vice
Chairman Thomas M. Hoenig, seconded by Director Jeremiah O. Norton
(Appointive), concurred in by Director Thomas J. Curry (Comptroller of
the Currency), Director Richard Cordray (Director, Consumer Financial
Protection Bureau), and Chairman Martin J. Gruenberg, that Corporation
business required its consideration of the matters which were to be the
subject of this meeting on less than seven days' notice to the public;
that no earlier notice of the meeting was practicable; that the public
interest did not require consideration of the matters in a meeting open
to public observation; and that the matters could be considered in a
closed meeting by authority of subsections (c)(4), (c)(6), (c)(8),
(c)(9)(A)(ii), and (c)(9)(B) of the ``Government in the Sunshine Act''
(5 U.S.C. 552b(c)(4), (c)(6), (c)(8), (c)(9)(A)(ii), and (c)(9)(B).
The meeting was held by telephone.
Dated: February 17, 2015.
Federal Deposit Insurance Corporation.
Robert E. Feldman,
Executive Secretary.
[FR Doc. 2015-03605 Filed 2-18-15; 4:15 pm]
BILLING CODE 6714-01-P