[Federal Register Volume 90, Number 204 (Friday, October 24, 2025)]
[Notices]
[Pages 48553-48554]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-19650]



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Notices
                                                Federal Register
________________________________________________________________________

This section of the FEDERAL REGISTER contains documents other than rules 
or proposed rules that are applicable to the public. Notices of hearings 
and investigations, committee meetings, agency decisions and rulings, 
delegations of authority, filing of petitions and applications and agency 
statements of organization and functions are examples of documents 
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Federal Register / Vol. 90, No. 204 / Friday, October 24, 2025 / 
Notices

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DEPARTMENT OF COMMERCE

Patent and Trademark Office


Agency Information Collection Activities; Submission to the 
Office of Management and Budget for Review and Approval; Comment 
Request; Requirements for Patent Applications Containing Nucleotide 
Sequence and/or Amino Acid Sequence Disclosures

AGENCY: United States Patent and Trademark Office, Department of 
Commerce.

ACTION: Notice of information collection; request for comments.

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SUMMARY: The United States Patent and Trademark Office (USPTO) will 
submit the following information collection request to the Office of 
Management and Budget (OMB) for review and clearance in accordance with 
the Paperwork Reduction Act of 1995, on or after the date of 
publication of this notice. The USPTO invites comments on this 
information collection renewal of 0651-0024 (Requirements for Patent 
Applications Containing Nucleotide Sequence and/or Amino Acid Sequence 
Disclosures), which helps the USPTO assess the impact of its 
information collection requirements and minimize the public's reporting 
burden. Public comments were previously requested via the Federal 
Register on June 26, 2025, during a 60-day comment period (90 FR 
27284). This notice allows for an additional 30 days for public 
comment.

DATES: To ensure consideration, you must submit comments regarding this 
information collection on or before November 24, 2025.

ADDRESSES: Written comments and recommendations for this information 
collection should be submitted within 30 days of the publication of 
this notice at the following website, www.reginfo.gov/public/do/PRAMain. Find this particular information collection by selecting 
``Currently under 30-day Review--Open for Public Comments'' or by using 
the search function and entering either the title of the information 
collection or the OMB Control Number, 0651-0024. Do not submit 
Confidential Business Information or otherwise sensitive or protected 
information.

FOR FURTHER INFORMATION CONTACT: 
     This information collection request may be viewed at 
www.reginfo.gov/public/do/PRAMain. Follow the instructions to view 
Department of Commerce, USPTO information collections currently under 
review by OMB.
     Email: [email protected]. Include ``0651-
0024 information request'' in the subject line of the message.
     Mail: Justin Isaac, Office of the Chief Administrative 
Officer, United States Patent and Trademark Office, P.O. Box 1450, 
Alexandria, VA 22313-1450.
     Telephone: Raul Tamayo, Senior Legal Advisor, (571)-272-
7728.

SUPPLEMENTARY INFORMATION: 
    Agency: United States Patent and Trademark Office, Department of 
Commerce.
    Title: Requirements for Patent Applications Containing Nucleotide 
Sequence and/or Amino Acid Sequence Disclosures.
    OMB Control Number: 0651-0024.
    Needs and Uses: Patent applications that contain nucleotide and/or 
amino acid sequence disclosures falling within the definitions of 37 
CFR 1.831 (for applications filed on or after July 1, 2022) or 37 CFR 
1.821(a) (for applications filed on or before June 30, 2022) must 
include, as a separate part of the application disclosure, a copy of 
the sequence listing in accordance with the requirements in 37 CFR 
1.831-1.835 or 37 CFR 1.821-1.825, respectively. Applicants may submit 
sequence listings for both U.S. and international patent applications. 
For more information concerning the submission of sequence listings in 
international applications, see the Patent Cooperation Treaty (PCT) 
Rules 5.2 and 13ter, Annex C of the PCT Administrative Instructions, 
and section 1848 of the Manual of Patent Examining Procedure (MPEP) 
(9th ed., Rev. 01.2024, November 2024).
    The USPTO uses the sequence listings during the examination process 
to determine the patentability of the invention claimed in the 
application. The USPTO also uses the sequence listings for pre-grant 
publication of applications and issued patents. Applicants use sequence 
listings when preparing both national and international patent 
applications that disclose nucleotide and/or amino acid sequences to 
provide a written description of the invention and to distinguish the 
claimed subject matter from the prior art.
    This information covers only the submission of sequence listing 
information itself. Information pertaining to the initial filing of a 
U.S. patent application is collected under OMB Control Number 0651-
0032, and information pertaining to the initial filing of international 
applications is collected under OMB Control Number 0651-0021.
    For sequence listings filed as 37 CFR 1.825 amendments in 
applications having a filing date of on or before June 30, 2022, this 
information collection also accounts for the submission of a new or 
substitute computer readable form (CRF) copy of the sequence listing 
under 37 CFR 1.821(e) and 1.824, with the amendment incorporated 
therein, if necessary, under 37 CFR 1.825(a)(5)(ii) or (b)(6)(ii).
    Forms: None.
    Type of Review: Extension and revision of a currently approved 
information collection.
    Affected Public: Public sector.
    Respondent's Obligation: Required to obtain or retain benefits.
    Frequency: On occasion.
    Estimated Number of Annual Respondents: 30,000 respondents.
    Estimated Number of Annual Responses: 30,000 responses.
    Estimated Time per Response: The USPTO estimates that the responses 
in this information collection will take the public approximately 6 
hours to complete. This includes the time to gather the necessary 
information, create the document, and submit the completed item(s) to 
the USPTO.
    Estimated Total Annual Respondent Burden Hours: 180,000 hours.

[[Page 48554]]

    Estimated Total Annual Respondent Non-hourly Cost Burden: $336,973.

Justin Isaac,
Information Collections Officer, Office of the Chief Administrative 
Officer, United States Patent and Trademark Office.
[FR Doc. 2025-19650 Filed 10-23-25; 8:45 am]
BILLING CODE 3510-16-P