Patent Trial and Appeal Board (PTAB) Appeals

Forms and Documents

Document Name	Status
Form PTO/AIA/32 Request for Rehearing Before the PTAB Form	Modified
Form PTO/SB/31 Notice of Appeal Form and Instruction	Modified
0651-0063 2024 Patent Fee Rule CWS.docx Justification for No Material/Nonsubstantive Change	2024-11-20
0651-0063 Supporting Statement 2023 Final.docx Supporting Statement A	2023-09-18
The Manual of Patent Examining Procedure.PDF Supplementary Document	2023-09-07
American Inventor's Protection Act of 1999.pdf Supplementary Document	2023-09-07
Leahy-Smith America Invents Act.pdf Supplementary Document	2023-09-07
USPTO Information Quality Guidelines.pdf Supplementary Document	2023-09-07

IC Document Collections

IC ID	Document Title	Status
262070	Statements, Motions, Oppositions, and Replies in preliminary and priority phases of an Interference	Unchanged
262069	Request for Rehearing Before the PTAB Form	Modified
242197	Notice of Appeal Form and Instruction	Modified

ICR Details

OMB Control No: 0651-0063	ICR Reference No: 202410-0651-008
Status: Received in OIRA	Previous ICR Reference No: 202304-0651-002
Agency/Subagency: DOC/PTO	Agency Tracking No:
Title: Patent Trial and Appeal Board (PTAB) Appeals
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 11/20/2024

	Requested	Previously Approved
Expiration Date	10/31/2026	10/31/2026
Responses	22,149	22,149
Time Burden (Hours)	238,999	238,999
Cost Burden (Dollars)	18,540,677	17,185,623

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Abstract: The Patent Trial and Appeal Board (PTAB or Board) is established by statute under 35 U.S.C. Section 6. This statute directs that PTAB "shall on written appeal of an applicant, review adverse decisions of examiners upon applications for patent and shall determine priority and patentability of invention in interferences." PTAB has the authority, under pre-AIA sections of the Patent Act, i.e. 35 U.S.C. Sections 134, 135, 306, and 315, to decide ex parte and inter partes appeals and interferences. The information in this information collection can be submitted in paper or electronically. In this renewal, the USPTO is adding the Petitions to the Chief Administrative Patent Judge Under 37 CFR 41.3 into the information collection, in addition to adjusting the responses, burden hours, and annual (non-hour) costs. The USPTO expects that businesses or other for-profits and non-profit institutions will mainly respond to this information collection, in addition to individuals or households.

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Authorizing Statute(s): US Code: 35 USC 134 and 135 Name of Law: America Invents Act
   US Code: 35 USC 6 Name of Law: American Inventor Protection Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	88 FR 42699	07/03/2023
30-day Notice:	Federal Register Citation:	Citation Date:
	88 FR 63940	09/18/2023
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 3

IC Title	Form No.	Form Name
Notice of Appeal	PTO/AIA/31, PTO/SB/31	Notice of Appeal from the Examiner to the Patent Trial and Appeal Board ,   Notice of Appeal from the Examiner to the Patent Trial and Appeal Board
Request for Rehearing Before the PTAB	PTO/AIA/32 , PTO/SB/32	Request for Oral Hearing Before the PTAB ,   Request for Oral Hearing Before the PTAB
Statements, Motions, Oppositions, and Replies in preliminary and priority phases of an Interference

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ICR Summary of Burden

	Total Request	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	22,149	22,149	0	0	0	0
Annual Time Burden (Hours)	238,999	238,999	0	0	0	0
Annual Cost Burden (Dollars)	18,540,677	17,185,623	0	1,355,054	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $294,249

Does this IC contain surveys, censuses, or employ statistical methods? No

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     Yes

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     Yes

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? No

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 11/20/2024

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