Patent Reexaminations, Supplemental Examinations, and Post Patent Submissions

ICR 202109-0651-005

OMB: 0651-0064

Federal Form Document

IC Document Collections
IC ID
Document
Title
Status
249731
New
249730 New
249729 New
249726
New
249723
New
249722
New
249720
New
200894
Modified
200893 Modified
200892 Modified
191641
Modified
191640
Modified
191639
Modified
191638
Modified
191637
Modified
191636
Modified
191635
Modified
191634
Modified
191629 Modified
191628 Modified
ICR Details
0651-0064 202109-0651-005
Received in OIRA 201909-0651-013
DOC/PTO
Patent Reexaminations, Supplemental Examinations, and Post Patent Submissions
Revision of a currently approved collection   No
Regular 10/19/2021
  Requested Previously Approved
36 Months From Approved 11/30/2021
880 1,745
23,574 38,086
2,439,335 2,884,393

The USPTO is required by 35 U.S.C. 131 and 151 to examine applications and, when appropriate, allow applications and issue them as patents. Chapter 30 of Title 35 U.S.C. provides that any person at any time may file a request for reexamination by the USPTO of any claim of a patent on the basis of prior art cited under the provisions of 35 U.S.C. 301. Once initiated, the reexamination proceedings under Chapter 30 are substantially ex parte and do not permit input from third parties. The regulations outlining ex parte reexaminations are found at 37 CFR 1.510-1.570. In addition, 35 U.S.C. 257 permits a patent owner to request supplemental examination of a patent by the USPTO to consider, reconsider, or correct information believed to be relevant to the patent. The regulations outlining supplemental examination are found at 37 CFR 1.601-1.625. The Leahy-Smith America Invents Act terminated inter partes reexamination effective September 16, 2012. However, inter partes reexamination proceedings based on inter partes reexamination requests filed before September 16, 2012, continue to be prosecuted. Therefore, this information collection continues to include items related to the prosecution of inter partes reexamination proceedings. The regulations outlining inter partes reexamination are found at 37 CFR 1.903-1.959. The provisions of 35 U.S.C. 301 and 37 CFR 1.501 govern the ability of a person to submit into the file of an issued patent (1) prior art consisting of patents or printed publications which the person making the submission believes to have a bearing on the patentability of any claim of the issued patent and (2) statements of the owner of the issued patent filed in a proceeding before a Federal court or the USPTO in which the owner of the issued patent took a position on the scope of any claim of the issued patent. This information collection covers information contained in: (1) requests for ex parte reexamination, (2) requests for supplemental examination, (3) submissions made by patent owners and third-party requesters related to the prosecution of an ex parte or inter partes reexamination proceeding, (4) information submitted by the public to aid in ascertaining the patentability and/or scope of the claims of the issued patent, and (5) information submitted by patent owners regarding a position taken before the USPTO or a Federal court regarding the scope of any claim in their issued patent. The USPTO’s use of the statements of the patent owners ((5) above) will be limited to determining the meaning of a patent claim in ex parte reexamination proceedings that already have been ordered and in inter partes review and post grant review proceedings that already have been instituted. The purpose of this information collection is to facilitate requests for ex parte reexamination and supplemental examination, to facilitate prosecution of reexamination and reissue proceedings, and to ensure that the associated documentation is submitted to the USPTO, and to permit relevant post-patent prior art and claim scope information to be entered into a patent file.

PL: Pub.L. 112 - 29 12 Name of Law: Leahy-Smith America Invents Act
  
None

Not associated with rulemaking

  86 FR 40015 07/26/2021
86 FR 57812 10/19/2021
No

20
IC Title Form No. Form Name
Amendment in Ex Parte or Inter Partes Reexamination - Individuals or Households
Amendment in Ex Parte or Inter Partes Reexamination - Private Sector
Information Disclosure Citation in a Patent - Individuals or Households PTO/SB/42 Information Disclosure Citation in a Patent
Information Disclosure Citation in a Patent - Private Sector PTO/SB/42 Information Disclosure Citation in a Patent
Patent Owner's 37 CFR 1.530 Statement - Individuals or Households
Patent Owner's 37 CFR 1.530 Statement - Private Sector
Patent Owner's 37 CFR 1.951 Response in Inter Partes Reexamination - Private Sector
Petition in a Reexamination Proceeding (except for those specifically enumerated in 37 CFR 1.550(i) and 1.937(d)) - Individuals or Households
Petition in a Reexamination Proceeding (except for those specifically enumerated in 37 CFR 1.550(i) and 1.937(d)) - Private Sector
Petition to Request Extension of Time in Ex Parte or Inter Partes Reexamination - Individuals or Households
Petition to Request Extension of Time in Ex Parte or Inter Partes Reexamination - Private Sector
Request for Ex Parte Reexamination - Individuals or Households PTO/SB/57 Request for Ex Parte Reexamination Transmittal Form
Request for Ex Parte Reexamination - Private Sector PTO/SB/57 Request for Ex Parte Reexamination Transmittal Form
Request for Supplemental Examination - Individuals or Households PTO/SB/59 Request for Supplemental Examination Transmittal Form
Request for Supplemental Examination - Private Sector PTO/SB/59 Request for Supplemental Examination Transmittal Form
Response to Final Rejection in Ex Parte Reexamination - Individuals or Households
Response to Final Rejection in Ex Parte Reexamination - Private Sector
Third Party Requester's 37 CFR 1.535 Reply - Private Sector
Third Party Requester's 37 CFR 1.947 Comments in Inter Partes Reexamination - Private Sector
Third Party Requester's 37 CFR 1.951 Comments in Inter Partes Reexamination - Private Sector

  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 880 1,745 0 49 -914 0
Annual Time Burden (Hours) 23,574 38,086 0 490 -15,002 0
Annual Cost Burden (Dollars) 2,439,335 2,884,393 0 0 -445,058 0
Yes
Miscellaneous Actions
No
Change in Respondents and Hourly Burden due to Adjustment in Agency Estimate The total number of respondents has decreased by 914 due to estimated fluctuations in the number of responses/submissions in this information collection. This decrease in the number of respondents and responses results in a decrease of 15,002 hours in the annual time burden estimates. Changes in Annual (Non-hour) Costs due to Adjustment in Agency Estimate For this renewal, the USPTO estimates that the total annual (non-hour) costs will decrease by $445,058 from the previous approval. This decrease is due to estimated fluctuations in submissions for items that require a fee. Change in Respondents and Hourly Burden due to Program Change due to Agency Discretion This renewal request incorporates an item that was previously approved under OMB control number 0651-0067 (Post Patent Public Submissions); specifically ‘information disclosure citations’. The merger of this item in this information collection results in response and burden increases due to this change. The estimated number of responses increases by 49 and the estimated number of burden hours increases by 490.

$57,391
No
    Yes
    Yes
No
No
No
No
Parikha Mehta 571 272-3248

  No

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:
 
 
 
 
 
 
 
    (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;
 
 
 
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.
10/19/2021


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