Notice of Agreement Filed, 50536 [2021-19483]
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50536
Federal Register / Vol. 86, No. 172 / Thursday, September 9, 2021 / Notices
FEDERAL ELECTION COMMISSION
Sunshine Act Meeting
Tuesday, September 14,
2021 at 10:00 a.m.
PLACE: 1050 First Street NE,
Washington, DC (this meeting will be a
virtual meeting).
STATUS: This meeting will be closed to
the public.
MATTERS TO BE CONSIDERED:
Compliance matters pursuant to 52
U.S.C. 30109.
Matters relating to internal personnel
decisions, or internal rules and
practices.
Investigatory records compiled for law
enforcement purposes and production
would disclose investigative
techniques.
Matters concerning participation in civil
actions or proceedings or arbitration.
*
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CONTACT PERSON FOR MORE INFORMATION:
Judith Ingram, Press Officer; Telephone:
(202) 694–1220.
TIME AND DATE:
Vicktoria J. Allen,
Acting Deputy Secretary of the Commission.
[FR Doc. 2021–19597 Filed 9–7–21; 4:15 pm]
also revise the agreement to replace
references to NYK with ONE and delete
provisions of the agreement relating to
the now complete transition to ONE.
The parties request expedited review.
Proposed Effective Date: 10/16/2021.
Location: https://www2.fmc.gov/
FMC.Agreements.Web/Public/
AgreementHistory/1972.
Dated: September 3, 2021.
Rachel E. Dickon,
Secretary.
[FR Doc. 2021–19483 Filed 9–8–21; 8:45 am]
BILLING CODE 6730–02–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2021–D–0875]
S12 Nonclinical Biodistribution
Considerations for Gene Therapy
Products; International Council for
Harmonisation; Draft Guidance for
Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
BILLING CODE 6715–01–P
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry entitled ‘‘S12
Nonclinical Biodistribution
Considerations for Gene Therapy
Products.’’ The draft guidance was
prepared under the auspices of the
International Council for Harmonisation
(ICH), formerly the International
Conference on Harmonisation. The draft
guidance provides harmonized
recommendations for the conduct and
overall design of nonclinical
biodistribution (BD) studies for gene
therapy (GT) products. Considerations
for interpretation and application of the
BD data to support a nonclinical
development program and inform the
design of clinical trials are also
provided. The recommendations in the
guidance endeavour to facilitate the
development of investigational GT
products, while avoiding unnecessary
use of animals, in accordance with the
3Rs (reduce/refine/replace) principles.
The draft guidance is intended to
promote harmonization of
recommendations for BD studies for
investigational GT products and
facilitate a more efficient and timely
nonclinical development program.
DATES: Submit either electronic or
written comments on the draft guidance
by November 8, 2021 to ensure that the
Agency considers your comment on this
SUMMARY:
FEDERAL MARITIME COMMISSION
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Notice of Agreement Filed
The Commission hereby gives notice
of the filing of the following agreement
under the Shipping Act of 1984.
Interested parties may submit
comments, relevant information, or
documents regarding the agreement to
the Secretary by email at Secretary@
fmc.gov, or by mail, Federal Maritime
Commission, Washington, DC 20573.
Comments will be most helpful to the
Commission if received within 12 days
of the date this notice appears in the
Federal Register. Copies of agreement
are available through the Commission’s
website (www.fmc.gov) or by contacting
the Office of Agreements at (202)–523–
5793 or tradeanalysis@fmc.gov.
Agreement No.: 012474–002.
Agreement Name: ONE/ELJSA Space
Charter Agreement.
Parties: Ocean Network Express Pte.
Ltd.; and Evergreen Line Joint Service
Agreement.
Filing Party: Joshua Stein; Cozen
O’Connor.
Synopsis: The amendment would
revise the agreement to reduce the total
amount of space that will be provided
by ONE to ELJSA and change the service
that such space will be provided on to
the FP1 service. The amendment would
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draft guidance before it begins work on
the final version of the guidance.
ADDRESSES: You may submit comments
on any guidance at any time as follows:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2021–D–0875 for ‘‘S12 Nonclinical
Biodistribution Considerations for Gene
Therapy Products.’’ Received comments
will be placed in the docket and, except
for those submitted as ‘‘Confidential
Submissions,’’ are publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday, 240–402–7500.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
E:\FR\FM\09SEN1.SGM
09SEN1
Agencies
[Federal Register Volume 86, Number 172 (Thursday, September 9, 2021)]
[Notices]
[Page 50536]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-19483]
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FEDERAL MARITIME COMMISSION
Notice of Agreement Filed
The Commission hereby gives notice of the filing of the following
agreement under the Shipping Act of 1984. Interested parties may submit
comments, relevant information, or documents regarding the agreement to
the Secretary by email at [email protected], or by mail, Federal
Maritime Commission, Washington, DC 20573. Comments will be most
helpful to the Commission if received within 12 days of the date this
notice appears in the Federal Register. Copies of agreement are
available through the Commission's website (www.fmc.gov) or by
contacting the Office of Agreements at (202)-523-5793 or
[email protected].
Agreement No.: 012474-002.
Agreement Name: ONE/ELJSA Space Charter Agreement.
Parties: Ocean Network Express Pte. Ltd.; and Evergreen Line Joint
Service Agreement.
Filing Party: Joshua Stein; Cozen O'Connor.
Synopsis: The amendment would revise the agreement to reduce the
total amount of space that will be provided by ONE to ELJSA and change
the service that such space will be provided on to the FP1 service. The
amendment would also revise the agreement to replace references to NYK
with ONE and delete provisions of the agreement relating to the now
complete transition to ONE. The parties request expedited review.
Proposed Effective Date: 10/16/2021.
Location: https://www2.fmc.gov/FMC.Agreements.Web/Public/AgreementHistory/1972.
Dated: September 3, 2021.
Rachel E. Dickon,
Secretary.
[FR Doc. 2021-19483 Filed 9-8-21; 8:45 am]
BILLING CODE 6730-02-P