Sterigenics International, Inc.; Withdrawal of Food Additive Petition, 39699-39700 [2010-16884]
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Federal Register / Vol. 75, No. 132 / Monday, July 12, 2010 / Notices
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Dated: July 6, 2010.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2010–16903 Filed 7–9–10; 8:45 am]
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outlined in this RFI, may submit
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fax 301–496–9839; e-mail
CFomous@od.nih.gov.
Dated: July 6, 2010.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[Docket No. FDA–2004–F–0069] (formerly
Docket No. 2004F–0455)
[FR Doc. 2010–16900 Filed 7–9–10; 8:45 am]
Dated: July 7, 2010.
Raynard S. Kington,
Deputy Director, National Institutes of Health.
[FR Doc. 2010–16904 Filed 7–9–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Sterigenics International, Inc.;
Withdrawal of Food Additive Petition
AGENCY:
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Food and Drug Administration,
HHS.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Request for Information (RFI) on the
National Institutes of Health Plan to
Develop the Genetic Testing Registry;
Notice
On June 11, 2010, the National
Institutes of Health (NIH), an agency
within the Department of Health and
Human Services (HHS), published a
Request for Information (RFI) on its plan
to develop a voluntary Genetic Testing
Registry (GTR), a centralized public
resource that will provide information
about the availability, scientific basis,
and usefulness of genetic tests (see Vol.
75, No. 112, page 33317). The NIH is
extending the comment period for the
RFI from July 12, 2010, to August 2,
2010. A copy of the RFI is also available
at https://www.ncbi.nlm.nih.gov/gtr/.
DATES: To ensure consideration,
comments must now be received by
August 2, 2010.
ADDRESSES: Individuals, groups, and
organizations interested in commenting
on the NIH plan to develop the GTR, as
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ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
withdrawal, without prejudice to a
future filing, of a food additive petition
(FAP 3M4744) proposing that the food
additive regulations be amended to
provide for the safe use of ionizing
radiation in the production of shelf
stable foods, including multiple
ingredient shelf stable foods.
FOR FURTHER INFORMATION CONTACT:
Lane A. Highbarger, Center for Food
Safety and Applied Nutrition (HFS–
255), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park,
MD 20740–3835, 301–436–1204.
SUPPLEMENTARY INFORMATION: In a notice
published in the Federal Register of
November 30, 2004 (69 FR 69606), FDA
announced that a food additive petition
(FAP 3M4744) had been filed by
Sterigenics International, Inc., P.O. Box
17349, Memphis, TN 31817–0349
(current address 2015 Spring Rd., suite
650, Oak Brook, IL 60523). The petition
proposed to amend the food additive
regulations in 21 CFR part 179
Irradiation in the Production, Processing
and Handling of Food to provide for the
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39700
Federal Register / Vol. 75, No. 132 / Monday, July 12, 2010 / Notices
safe use of ionizing radiation in the
production of fully cooked shelf stable
foods, including fully cooked multiple
ingredient shelf stable foods, where the
absorbed dose required to cause a 12-log
reduction in Clostridium botulinum has
been established. Sterigenics
International, Inc., has now withdrawn
the petition without prejudice to a
future filing (21 CFR 171.7).
Dated: June 30, 2010.
Mitchell A. Cheeseman,
Acting Director, Office of Food Additive
Safety, Center for Food Safety and Applied
Nutrition.
[FR Doc. 2010–16884 Filed 7–12–10; 8:45 am]
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DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
[USCG–2010–0560]
Information Collection Request to
Office of Management and Budget;
OMB; Control Number: 1625–New
Coast Guard, DHS.
Sixty-day notice requesting
comments.
AGENCY:
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ACTION:
SUMMARY: In compliance with the
Paperwork Reduction Act of 1995, the
U.S. Coast Guard intends to submit an
Information Collection Request (ICR)
and Analysis to the Office of
Management and Budget (OMB)
requesting an approval for the following
collection of information: 1625–New,
Port Stakeholder Interface Form. Before
submitting this ICR to OMB, the Coast
Guard is inviting comments as
described below.
DATES: Comments must reach the Coast
Guard on or before September 10, 2010.
ADDRESSES: To avoid duplicate
submissions to the docket [USCG–2010–
0560], please use only one of the
following means:
(1) Online: https://
www.regulations.gov.
(2) Mail: Docket Management Facility
(DMF) (M–30), U.S. Department of
Transportation (DOT), West Building
Ground Floor, Room W12–140, 1200
New Jersey Avenue, SE., Washington,
DC 20590–0001.
(3) Hand deliver: Same as mail
address above, between 9 a.m. and 5
p.m., Monday through Friday, except
Federal holidays. The telephone number
is 202–366–9329.
(4) Fax: 202–493–2251.
The DMF maintains the public docket
for this Notice. Comments and material
received from the public, as well as
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documents mentioned in this Notice as
being available in the docket, will
become part of the docket and will be
available for inspection or copying at
room W12–140 on the West Building
Ground Floor, 1200 New Jersey Avenue,
SE., Washington, DC, between 9 a.m.
and 5 p.m., Monday through Friday,
except Federal holidays. You may also
find the docket on the Internet at
https://www.regulations.gov.
A copy of the ICR is available through
the docket on the Internet at https://
www.regulations.gov. Additionally,
copies are available from:
Commandant (CG–611), ATTN
Paperwork Reduction Act Manager,
US Coast Guard, 2100 2ND ST SW.
STOP 7101, Washington, DC 20593–
7101.
FOR FURTHER INFORMATION CONTACT:
Contact Mr. Arthur Requina, Office of
Information Management, telephone
202–475–3523, or fax 202–475–3929, for
questions on these documents. Contact
Ms. Renee V. Wright, Program Manager,
Docket Operations, 202–366–9826, for
questions on the docket.
SUPPLEMENTARY INFORMATION:
Public Participation and Request for
Comments
The Coast Guard invites comments on
whether this ICR should be granted
based on the collection being necessary
for the proper performance of
Departmental functions. In particular,
the Coast Guard would appreciate
comments addressing: (1) The practical
utility of the collection; (2) the accuracy
of the estimated burden of the
collection; (3) ways to enhance the
quality, utility, and clarity of
information subject to the collection;
and (4) ways to minimize the burden of
the collections on respondents,
including the use of automated
collection techniques or other forms of
information technology.
We encourage you to respond to this
request by submitting comments and
related materials. We will post all
comments received, without change, to
https://www.regulations.gov. They will
include any personal information you
provide. We have an agreement with
DOT to use their DMF. Please see the
‘‘Privacy Act’’ paragraph below.
Submitting comments: If you submit a
comment, please include the docket
number [USCG–2010–0560], indicate
the specific section of the document to
which each comment applies, providing
a reason for each comment. We
recommend you include your name,
mailing address, an e-mail address, or
other contact information in the body of
your document so that we can contact
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you if we have questions regarding your
submission. You may submit your
comments and material by electronic
means, mail, fax, or delivery to the DMF
at the address under ADDRESSES; but
please submit them by only one means.
If you submit them by mail or delivery,
submit them in an unbound format, no
larger than 8–1⁄2 by 11 inches, suitable
for copying and electronic filing.
If you submit them by mail and would
like to know that they reached the
Facility, please enclose a stamped, selfaddressed postcard or envelope. We will
consider all comments and material
received during the comment period
and will address them accordingly.
Viewing comments and documents:
Go to https://www.regulations.gov to
view documents mentioned in this
Notice as being available in the docket.
Click on the ‘‘read comments’’ box,
which will then become highlighted in
blue. In the ‘‘Keyword’’ box insert
‘‘USCG–2010–0560 ’’ and click ‘‘Search.’’
Click the ‘‘Open Docket Folder’’ in the
‘‘Actions’’ column. You may also visit
the DMF in room W12–140 on the West
Building Ground Floor, 1200 New Jersey
Avenue, SE., Washington, DC, between
9 a.m. and 5 p.m., Monday through
Friday, except Federal holidays.
Privacy Act: Anyone can search the
electronic form of all comments
received in dockets by the name of the
individual submitting the comment (or
signing the comment, if submitted on
behalf of an association, business, labor
union, etc.). You may review the
Privacy Act statement regarding our
public dockets in the January 17, 2008
issue of the Federal Register (73 FR
3316).
Information Collection Request
Title: Port Stakeholder Interface Form.
OMB Control Number: 1625–New.
Summary: This information is needed
to ensure the Coast Guard can gather
critical cargo information from port
stakeholders in the event of a port
closure or disruption to the Marine
Transportation System.
Need: Section 202 of Public Law 109–
347 authorizes the Secretary Department
of Homeland Security to develop and
update, as necessary, protocols for the
resumption of trade in the event of a
transportation disruption/security
incident. It further instructs that
appropriate factors be considered for
establishing prioritization of vessels and
cargo determined by the President to be
critical for response and recovery,
including factors relating to public
health, national security, and economic
need.
Forms: CG–3142.
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[Federal Register Volume 75, Number 132 (Monday, July 12, 2010)]
[Notices]
[Pages 39699-39700]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-16884]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2004-F-0069] (formerly Docket No. 2004F-0455)
Sterigenics International, Inc.; Withdrawal of Food Additive
Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing the
withdrawal, without prejudice to a future filing, of a food additive
petition (FAP 3M4744) proposing that the food additive regulations be
amended to provide for the safe use of ionizing radiation in the
production of shelf stable foods, including multiple ingredient shelf
stable foods.
FOR FURTHER INFORMATION CONTACT: Lane A. Highbarger, Center for Food
Safety and Applied Nutrition (HFS-255), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park, MD 20740-3835, 301-436-1204.
SUPPLEMENTARY INFORMATION: In a notice published in the Federal
Register of November 30, 2004 (69 FR 69606), FDA announced that a food
additive petition (FAP 3M4744) had been filed by Sterigenics
International, Inc., P.O. Box 17349, Memphis, TN 31817-0349 (current
address 2015 Spring Rd., suite 650, Oak Brook, IL 60523). The petition
proposed to amend the food additive regulations in 21 CFR part 179
Irradiation in the Production, Processing and Handling of Food to
provide for the
[[Page 39700]]
safe use of ionizing radiation in the production of fully cooked shelf
stable foods, including fully cooked multiple ingredient shelf stable
foods, where the absorbed dose required to cause a 12-log reduction in
Clostridium botulinum has been established. Sterigenics International,
Inc., has now withdrawn the petition without prejudice to a future
filing (21 CFR 171.7).
Dated: June 30, 2010.
Mitchell A. Cheeseman,
Acting Director, Office of Food Additive Safety, Center for Food Safety
and Applied Nutrition.
[FR Doc. 2010-16884 Filed 7-12-10; 8:45 am]
BILLING CODE 4160-01-S