Sunshine Act Meetings, 9495-9496 [2023-03179]
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Federal Register / Vol. 88, No. 30 / Tuesday, February 14, 2023 / Notices
of Rights 4 and the AI Risk Management
Framework 5 within the innovation
ecosystem?
9. What statutory changes, if any,
should be considered as to U.S.
inventorship law, and what
consequences do you foresee for those
statutory changes? For example:
a. Should AI systems be made eligible
to be listed as an inventor? Does
allowing AI systems to be listed as an
inventor promote and incentivize
innovation?
b. Should listing an inventor remain
a requirement for a U.S. patent?
10. Are there any laws or practices in
other countries that effectively address
inventorship for inventions with
significant contributions from AI
systems?
11. The USPTO plans to continue
engaging with stakeholders on the
intersection of AI and intellectual
property. What areas of focus (e.g.,
obviousness, disclosure, data
protection) should the USPTO prioritize
in future engagements?
Katherine K. Vidal,
Under Secretary of Commerce for Intellectual
Property and Director of the United States
Patent and Trademark Office.
[FR Doc. 2023–03066 Filed 2–13–23; 8:45 am]
BILLING CODE 3510–16–P
DEPARTMENT OF COMMERCE
Patent and Trademark Office
[Docket No.: PTO–P–2021–0037]
Sixth Extension of the Modified
COVID–19 Prioritized Examination Pilot
Program for Patent Applications
United States Patent and
Trademark Office, Department of
Commerce.
ACTION: Notice.
AGENCY:
To continue to support the
acceleration of innovations in the fight
against COVID–19 during the public
health emergency, the United States
Patent and Trademark Office (USPTO or
Office) is extending the modified
COVID–19 Prioritized Examination Pilot
Program, which provides prioritized
examination of certain patent
applications. Requests that are
compliant with the pilot program’s
requirements and are filed on or before
May 11, 2023, will be accepted.
DATES: The COVID–19 Prioritized
Examination Pilot Program is extended
ddrumheller on DSK120RN23PROD with NOTICES
SUMMARY:
4 See https://www.whitehouse.gov/ostp/ai-bill-ofrights/.
5 See https://www.nist.gov/itl/ai-riskmanagement-framework.
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as of February 14, 2023, to run until
May 11, 2023.
FOR FURTHER INFORMATION CONTACT: Raul
Tamayo, Senior Legal Advisor, Office of
Patent Legal Administration (571–272–
77285, raul.tamayo@uspto.gov).
SUPPLEMENTARY INFORMATION: In 2020,
the USPTO published a notice on the
implementation of the COVID–19
Prioritized Examination Pilot Program.
See COVID–19 Prioritized Examination
Pilot Program, 85 FR 28932 (May 14,
2020) (COVID–19 Track One Notice).
The pilot program was implemented to
support the acceleration of innovations
in the fight against COVID–19. The
COVID–19 Track One Notice indicated
that an applicant may request
prioritized examination without
payment of the prioritized examination
fee and associated processing fee if: (1)
the patent application’s claim(s) covered
a product or process related to COVID–
19, (2) the product or process was
subject to an applicable Food and Drug
Administration (FDA) approval for
COVID–19 use, and (3) the applicant
met other requirements noted in the
COVID–19 Track One Notice.
Since the COVID–19 Track One
Notice, the USPTO has modified the
pilot program by removing the limit on
the number of patent applications that
could receive prioritized examination
and extending the pilot program five
times through notices published in the
Federal Register. The most recent notice
(87 FR 78661, December 22, 2022)
extended the program until February 15,
2023.
As of January 9, 2023, 364 patents had
issued from applications granted
prioritized status under the pilot
program. The average total pendency for
those applications was 356 days. The
shortest pendency from filing date to
issue date for those applications was 75
days.
The USPTO is further extending the
pilot program by setting the expiration
date as May 11, 2023. The extension
aligns with the January 30, 2023,
announcement by the White House that
it plans to extend the public health
emergency to May 11, 2023, and then
end it on that date. See
www.whitehouse.gov/wp-content/
uploads/2023/01/SAP-H.R.-382-H.J.Res.-7.pdf.
Following the expiration of this
extension, the pilot program will be
terminated in favor of the Office
dedicating its resources to its other
prioritized examination programs.
Patent applicants interested in
expediting the prosecution of their
patent application may instead seek to
use the Prioritized Examination (Track
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9495
One) Program. Patent applications
accorded prioritized examination under
the pilot program will not lose that
status merely because the application is
still pending after the date the pilot
program is terminated but will instead
retain prioritized examination status
until that status is terminated for one or
more reasons, as described in the
COVID–19 Track One Notice.
The Track One Program permits an
applicant to have a patent application
advanced out of turn (accorded special
status) for examination under 37 CFR
1.102(e) if the applicant timely files a
request for prioritized (Track One)
examination accompanied by the
appropriate fees and meets the other
conditions of 37 CFR 1.102(e). See
§ 708.02(b)(2) of the Manual of Patent
Examining Procedure (9th ed., rev.
10.2019, June 2020). The current
USPTO fee schedule is available at
www.uspto.gov/Fees.
The Track One Program does not have
the restrictions of the COVID–19
Prioritized Examination Pilot Program
regarding the types of inventions for
which special status may be sought, as
the Track One Program does not require
a connection to any particular
technology. Moreover, under the Track
One Program, an applicant can avoid
delays associated with the
determination of whether a patent
application presents a claim that covers
a product or process related to COVID–
19 and whether the product or process
is subject to an applicable FDA approval
for COVID–19 use.
Katherine K. Vidal,
Under Secretary of Commerce for Intellectual
Property and Director of the United States
Patent and Trademark Office.
[FR Doc. 2023–03216 Filed 2–13–23; 8:45 am]
BILLING CODE 3510–16–P
COMMODITY FUTURES TRADING
COMMISSION
Sunshine Act Meetings
FEDERAL REGISTER CITATION OF PREVIOUS
ANNOUNCEMENT: 88 FR 8262, February 8,
2023.
PREVIOUSLY ANNOUNCED TIME AND DATE OF
THE MEETING: 1:00 p.m. EST,
Wednesday, February 15, 2023.
The place of
the meeting has changed. This meeting
will now take place virtually. The
meeting time and date, Closed status,
and matters to be considered, as
previously announced, remain
unchanged.
CHANGES IN THE MEETING:
CONTACT PERSON FOR MORE INFORMATION:
Christopher Kirkpatrick, 202–418–5964.
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9496
Federal Register / Vol. 88, No. 30 / Tuesday, February 14, 2023 / Notices
Authority: 5 U.S.C. 552b.
SUPPLEMENTARY INFORMATION:
Dated: February 9, 2023.
Christopher Kirkpatrick,
Secretary of the Commission.
[FR Doc. 2023–03179 Filed 2–10–23; 11:15 am]
BILLING CODE 6351–01–P
CONSUMER PRODUCT SAFETY
COMMISSION
[Docket No. CPSC–2010–0041]
Collection of Information; Proposed
Extension of Approval; Comment
Request—Publicly Available Consumer
Product Safety Information Database
Consumer Product Safety
Commission.
ACTION: Notice.
AGENCY:
As required by the Paperwork
Reduction Act of 1995 (PRA), the
Consumer Product Safety Commission
(CPSC) announces that the CPSC has
submitted to the Office of Management
and Budget (OMB) a request for
extension of approval of a collection of
information for the Publicly Available
Consumer Product Safety Information
Database, previously under OMB
Control No. 3041–0146. On December 8,
2022, the CPSC published a notice in
the Federal Register announcing the
agency’s intent to seek this extension.
CPSC received one comment in support
of the collection of information in
response to that notice. By publication
of this notice, the Commission
announces that CPSC has submitted to
the OMB a request for extension of
approval of that collection of
information, without change.
DATES: Written comments on this
request for extension of approval of
information collection requirements
should be submitted by March 16, 2023.
ADDRESSES: Submit comments about
this request by email: OIRA_
submission@omb.eop.gov or fax: 202–
395–6881. Comments by mail should be
sent to the Office of Information and
Regulatory Affairs, Attn: OMB Desk
Officer for the CPSC, Office of
Management and Budget, Room 10235,
725 17th Street NW, Washington, DC
20503. In addition, written comments
that are sent to OMB, also should be
submitted electronically at: https://
www.regulations.gov, under Docket No.
CPSC–2010–0041.
FOR FURTHER INFORMATION CONTACT: For
further information, or a copy of the
supporting statement, contact: Cynthia
Gillham, Consumer Product Safety
Commission, 4330 East West Highway,
Bethesda, MD 20814; (301) 504–7791, or
by email to: cgillham@cpsc.gov.
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SUMMARY:
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A. Background
Section 212 of the Consumer Product
Safety Improvement Act of 2008
(CPSIA) added to the Consumer Product
Safety Act (CPSA) a new section 6A,
which requires the CPSC to establish
and maintain a publicly available,
searchable database (Database) on the
safety of consumer products and other
products or substances regulated by the
CPSC. Among other things, section 6A
requires the CPSC to collect reports of
harm from the public for potential
publication in the publicly available
Database, and to collect and publish
comments from manufacturers about
reports of harm.
In a proposed rule published on May
24, 2010 (75 FR 29156), the CPSC
announced that a proposed collection of
information in conjunction with the
Database, called the Publicly Available
Consumer Product Safety Information
Database, had been submitted to OMB
for review and clearance under 44
U.S.C. 3501–3520. The CPSC issued a
final rule on the Database on December
9, 2010 (75 FR 76832). The final rule
interprets various statutory
requirements in section 6A of the CPSA
pertaining to the information to be
included in the Database. The final rule
also establishes provisions regarding
submitting reports of harm; providing
notice of reports of harm to
manufacturers; publishing reports of
harm and manufacturer comments in
the Database; and dealing with
confidential and materially inaccurate
information.
OMB approved the collection of
information for the Database under
control number 3041–0146. OMB’s most
recent extension of approval, issued on
March 31, 2020, will expire on March
31, 2023. Accordingly, the CPSC is
seeking an extension of approval of this
collection of information.
B. Response To Comment
One individual commenter stated that
this collection of information is
necessary for general consumer safety,
but that the public lacks knowledge of
the Database. The commenter states that
CPSC should prioritize a campaign
regarding the existence and purpose of
the Database to benefit consumers. The
commenter states that the burden
estimates could be reduced through
automated and electronic collection
techniques, and that these options
should be explored, but that CPSC must
maintain data quality. CPSC appreciates
the commenter’s feedback and generally
agrees with the commenter’s statements.
CPSC is not making any changes to the
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burden estimates for this information
collection based on this comment.
C. Information Collected Through the
Database
The primary purpose of this
information collection is to populate the
publicly searchable Database of
consumer product safety information
mandated by section 6A of the CPSA.
The Database information collection has
four components: reports of harm,
manufacturer comments, branding
information, and the Small Batch
Manufacturer Registry (SBMR).
Reports of Harm: Reports of harm
communicate information regarding an
injury, illness, or death, or any risk (as
determined by CPSC) of injury, illness,
or death, relating to the use of a
consumer product or other product or
substance regulated by the CPSC.
Reports can be submitted to the CPSC
by consumers; local, state, or federal
government agencies; healthcare
professionals; child service providers;
public safety entities; and others.
Reports may be submitted via the CPSC
website (www.SaferProducts.gov), by
telephone via a CPSC call center, or by
email, fax, or mail using the incident
report form (available for download or
printing via the CPSC website). Reports
may also originate as a free-form letter
or email. Submitters must consent to
including their report of harm in the
publicly searchable Database.
Manufacturer Comments: Pursuant to
the CPSIA, CPSC transmits a report of
harm to the manufacturer or private
labeler identified in the report, and the
manufacturer or private labeler may
then submit a comment to CPSC related
to the report of harm (hereinafter
‘‘manufacturer comment’’).
Manufacturer comments may be
submitted through the business portal,
by email, mail, or fax. The business
portal is a feature of the Database that
allows manufacturers and private
labelers who register on the business
portal to receive reports of harm and
comment on such reports through the
business portal. Use of the business
portal expedites the receipt of reports of
harm and business response times.
A manufacturer or private labeler may
request that the CPSC designate
information in a report of harm as
confidential. Such a request may be
made using the business portal, by
email, by mail, or by fax. Additionally,
any person or entity reviewing a report
of harm or comment from a
manufacturer or private labeler, either
before or after publication in the
Database, may request that the report or
comment, or portions of the report or
comment, be excluded from the
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Agencies
[Federal Register Volume 88, Number 30 (Tuesday, February 14, 2023)]
[Notices]
[Pages 9495-9496]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-03179]
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COMMODITY FUTURES TRADING COMMISSION
Sunshine Act Meetings
FEDERAL REGISTER CITATION OF PREVIOUS ANNOUNCEMENT: 88 FR 8262,
February 8, 2023.
PREVIOUSLY ANNOUNCED TIME AND DATE OF THE MEETING: 1:00 p.m. EST,
Wednesday, February 15, 2023.
CHANGES IN THE MEETING: The place of the meeting has changed. This
meeting will now take place virtually. The meeting time and date,
Closed status, and matters to be considered, as previously announced,
remain unchanged.
CONTACT PERSON FOR MORE INFORMATION: Christopher Kirkpatrick, 202-418-
5964.
[[Page 9496]]
Authority: 5 U.S.C. 552b.
Dated: February 9, 2023.
Christopher Kirkpatrick,
Secretary of the Commission.
[FR Doc. 2023-03179 Filed 2-10-23; 11:15 am]
BILLING CODE 6351-01-P