The Latest Attempt to Expose SAWS Highlights Structural Flaws at the USPTO

“The government’s narrative cannot be allowed to rest on the testimony of a witness who by her own admission is not competent because she admitted to having no firsthand knowledge.”

sawsWhether or not the United States Patent and Trademark Office (USPTO) wants to admit it, over most of the last generation there has been a secret examination docket. Not surprisingly, such a secret examination docket is strictly prohibited by federal law. A newly filed joint status report in Morinville v. USPTO brings this issue to the fore and underscores the lack of transparency and accountability of secret internal patent review programs at the USPTO. Procedurally, the latest filing seeks to expose the USPTO shadow docket through a new round of discovery, which is currently being considered by the United States District Court for the District of Columbia.

Where It All Started

Perhaps the most often discussed secret review program of the last 30 years was the USPTO’s Sensitive Application Warning System (SAWS), which was an internal, non-public program that operated from 1994–2015. SAWS flagged certain patent applications deemed “sensitive” for elevated management oversight and additional layers of review before allowance, ostensibly as a quality-control mechanism to ensure that controversial, high-impact, or otherwise noteworthy inventions were not issued without scrutiny. In practice, however, SAWS was a secretive system with applicants not informed they had been assigned to this pit of despair from which patents would never issue.

This de facto suppression of applications caught in the SAWS snare occurred without transparency or due process and violated federal law. Specifically, 35 U.S.C. § 132 requires the USPTO to provide applicants with notice of rejections and the reasons therefor—something that, as a matter of administrative law and practice, must be memorialized in the written record. This statutory baseline is operationalized through 37 C.F.R. § 1.2, which requires business with the Office to be in writing, and specifically requires action of the USPTO to “be based exclusively on the written record in the Office.” And 35 U.S.C. 122 and 37 C.F.R. § 1.211 require the publication of applications, which include all filings and correspondence, unless the application is no longer pending, a national security order has been issued, or the applicant requested non-publication. Simply stated, this all means it should be legally impossible for the USPTO to operate a secret, shadow docket, but we know they did in SAWS because they have admitted to doing so.

Large Patent Families, OPQA and the Return of SAWS

The topic of large patent families spurred by continuation filings has sparked much controversy over the last several years. As a result, the Office of Patent Quality Assurance (OPQA) at the USPTO conducted a review of large patent families between November of 2021 and May 2025—the so-called Large Patent Family Review Program. Office actions reviewed by OPQA have not been identified to the public and were similarly unknown to applicants. The purpose of such a review was ostensibly to provide the examining corps with information to assist in improving the quality of issued patents. See MPEP 1308.03.

The quality assurance protocol authorized by MPEP 1308.03 is intended not to be used to affect allowance decisions, but instead to be used as an educational tool to aid in identifying best practices and problem areas. Id. To that end, if OPQA identifies an error, the MPEP specifically requires the reopening of the case, which would require applicants to be notified.  Id.

Based on our reporting, the so-called Large Patent Family Review Program was not simply to learn what is happening relative to the largest patent families, and it was not simply to use the obtained insights for educational purposes to establish best practices. Although not entirely clear due to a real lack of transparency, it seems that this Large Patent Family Review Program morphed into what can only be characterized as a SAWS reboot.

IPWatchdog has learned that when OPQA identified errors—which occurred prior to allowance—the applications were returned to examiners. Prosecution was not reopened and applicants were not notified, all of which is eerily reminiscent of the SAWS program. The views of OPQA were passed to examiners who then secretly changed allowance decisions unbeknownst to applicants, which makes this large patent family “quality review” yet another secret, shadow docket that violates federal law.

It is worth noting that OPQA-identified issues can and do trigger closer supervisory attention, which impacts an examiner’s record. As examiners and former examiners have repeatedly explained to IPWatchdog, no examiner wants to go against OPQA. This means OPQA gets what they want. If a quality reviewer wants more patent eligibility rejections that is what examiners deliver. If they want more obviousness rejections that is likewise what examiners deliver. So, it is entirely disingenuous for the Office to claim examiners have a real choice whether to allow a case when OPQA identifies errors and returns an application previously marked for allowance. When OPQA flags something, they get what they want, period. That makes them not the examiner assigned the ultimate decision-maker. That this happens unknown to the applicant and public violates federal law.

More Discovery Please

At issue in the latest filing in Morinville v. USPTO is whether additional discovery should be permitted. The impetus for this request was an April 13, 2026, deposition of Dr. Kathleen Bragdon, who is now Deputy Director of the OPQA. In that recent deposition, Bragdon’s testimony reveals insights into the Large Patent Family Review Program—and its potential relationship to prior controversial initiatives such as SAWS.

Make no mistake, this is not just another procedural skirmish over discovery. At a high level, this discovery dispute is about governance: who knows what inside the agency, how that knowledge is documented, whether internal quality initiatives operate with sufficient transparency to withstand judicial scrutiny, and to what extent is the USPTO violating federal laws that require all decisions to be memorialized in writing, with the applicant and public being informed.

The Inquiry That Reignited the SAWS Dispute

In June 2025 a Department of Justice (DOJ) investigation letter from then–DOJ official Edward Martin, Director of the Weaponization Working Group, (the “DOJ letter”) raised serious allegations about “weaponization” in the form of a continuation of the allegedly “retired” SAWS program. In essence, the DOJ letter asserted that the USPTO was still operating the SAWS program in 2025 to “secretly flag… allowable patent applications to prevent them from issuing.”

The DOJ letter framed this SAWS process as an investigation of “weaponization of [USPTO] policies and procedures against American companies and inventors” without even a mention of a “quality” program. But now the USPTO makes up a counterfactual story that the DOJ letter was really about a public quality program instead of the continuing secret SAWS program, even though the DOJ letter is focused on the expressly stated secret SAWS program and does not even mention a quality program. This USPTO argument does not ring true. Yes, there was a large patent family review, but that review went well beyond quality, education and best practices for the future and morphed into OPQA telling examiners that they could do what they want, but in the view of OPQA they are about to make an error. And even that second pair of eyes review—which isn’t supposed to happen—wouldn’t be as nefarious as what happened. If there was really nothing wrong with what OPQA was doing, then why not reopen prosecution as the MPEP demands and notify the applicant? That this was kept secret from the applicant and public is the problem and screams that the Office knew what was happening was prohibited.

A Deposition That Raised More Questions Than It Answered

The plaintiffs’ position in the pending discovery dispute hinges on a central claim: that Dr. Bragdon’s prior declaration—used by the USPTO to resist reopening discovery—was not grounded in firsthand knowledge and she could not answer important relevant questions. According to the filing, her deposition testimony revealed limited personal familiarity with key aspects of the Large Patent Family Review Program, including its mechanics, scope, and relationship to other initiatives.

Most notably, Dr. Bragdon acknowledged that she lacked direct knowledge regarding the external catalyst for the dispute: the June 2025 DOJ letter that was specifically directed toward uncovering a “SAWS program”. When pressed on that issue, she testified unequivocally: “I have no personal knowledge of the circumstances referred to in the Martin letter.”

That admission has become a focal point for plaintiffs, who argue it undermines the government’s earlier reliance on her declaration to characterize the program at issue. If the agency’s principal declarant lacked visibility into the triggering allegations, plaintiffs contend, additional discovery is not only justified but necessary to get to the truth. The government’s narrative cannot be allowed to rest on the testimony of a witness who by her own admission is not competent because she admitted to having no firsthand knowledge.

Institutional Knowledge vs. Organizational Structure

Beyond the DOJ letter, the deposition surfaces a deeper structural issue: the fragmentation of knowledge within the USPTO’s quality review ecosystem. Dr. Bragdon acknowledged both the breadth of OPQA’s current role and its limitations. While she characterized OPQA as the “cornerstone” of quality review within the agency, she also conceded that other units may operate independent programs without full coordination. In her words: “The Office of Patent Quality Assurance is often consulted as the cornerstone quality group… but it’s quite possible we would not be.”

That admission introduces ambiguity into the government’s position that no undisclosed or analogous program exists. Plaintiffs are now leveraging that ambiguity to justify expanded discovery, including depositions of other USPTO personnel and requests for internal documents, data sets, and program criteria, all of which seems essential given the Director of OPQA has admitted that it is “quite possible” OPQA is not the only unit within the USPTO conducting quality reviews.

The institutional evolution of OPQA further complicates the analysis. Dr. Bragdon emphasized that the Office has expanded significantly since the era of the SAWS program, both in size and in influence. Yet she also confirmed that SAWS itself operated outside OPQA’s purview, saying in a declarative manner that “SAWS was not run by the Office of Patent Quality Assurance.”

For plaintiffs, that historical precedent matters. It demonstrates that major review programs can exist—and operate—without centralized oversight from the agency’s primary quality body. That fact fundamentally undercuts any categorical assertion that OPQA visibility equates to agency-wide awareness.

Competing Narratives: Clarification vs. ‘Fishing Expedition’

The USPTO, for its part, frames the deposition very differently. The agency argues that plaintiffs are attempting to “go on a fishing expedition” years after discovery closed, seeking to expand the case beyond its original scope.

In its view, Dr. Bragdon provided extensive testimony confirming that the Large Patent Family Review Program was a legitimate quality initiative, distinct from SAWS, and not reflective of the allegations in the DOJ letter. Of course, while it may initially, and structurally have been distinct from SAWS, there are serious questions about what it became. The secrecy elements, lack of transparency and violation of federal laws regarding decisions being memorialized in writing and made a part of the file are all points of worrying commonality with SAWS, which is why the DOJ letter expressly addresses the SAWS program over and over again.

What Comes Next

No one is challenging the Office’s right to conduct quality review aimed at identifying best practices and creating a better patent system. What is being questioned is whether what started out with laudable goals morphed into a secret, shadow docket that violates federal law.

The court now faces a classic discovery management decision: whether the plaintiffs have shown sufficient cause to expand the record, or whether the existing testimony closes the loop. Given the primary declarant admits to being unfamiliar with the salient facts and also admits that SAWS was not an OPQA initiative and that other entities within the Office can and do conduct their own reviews outside of the OPQA structure, additional discovery seems necessary to get to the truth.

Regardless of how the court ultimately rules on additional discovery, the dispute has broader implications for patent system governance. If additional discovery is permitted, the case could evolve into a broader examination of USPTO internal processes, including how applications are selected for enhanced review, how data is used to guide examiner behavior, and whether those practices are consistently disclosed. That would be a very good thing for the system as a whole. If additional discovery is not granted, the agency’s current framing—that the Large Patent Family Review Program is a benign quality initiative unrelated to the allegations at issue—will stand largely untested.

Either way, the litigation is no longer just about one program. It has become a proxy for a larger conversation about how the patent system manages risk, enforces quality, and communicates those efforts to stakeholders operating outside the agency.

 

 

 

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13 comments so far. Add my comment.

  • [Avatar for Ron Katznelson]
    Ron Katznelson
    May 7, 2026 03:29 pm

    To Mark Whitmer,
    You are correct that “Chinese applications receiving much less US examination scrutiny based on a Chinese determination of patentability under Chinese laws” should be a major concern to us all. However, your conclusion that I am instead “fixated” on “Chinese applicants receiving cheaper accelerated examination” is a false insult.

    First, you apparently missed my earlier comments on USPTO granting PPH entry to applications through blind reliance on foreign claim allowance without verifying the content of the documents submitted in foreign language with no translation that were the basis for such allowance. The fact that the USPTO in “PPH 2.0” created an express path for such implicit reliance is a major concern that I have raised, and you have apparently missed.

    Second, I raised the PPH fee waiver not as the basis of “Chinese applicants receiving cheaper accelerated examination,” but as a general USPTO violation of law in all PPH applications – issuing a substantive discriminatory rule with no statutory authority to do so, and without notice and comment rulemaking as required under the APA, 5 U.S.C. § 553. This discriminatory rule applies not for a select few cases, but to more than 8,900 PPH applications in FY2025 alone.

  • [Avatar for IamI]
    IamI
    May 7, 2026 01:40 pm

    I mean, Ron said, “Please provide evidence that examiners claim “that the USPTO is allowing significantly less examination time for PPH cases than non-PPH filings.” There is none that I am aware of.” I did that, then he dismissively brushed it off.

  • [Avatar for Mark Whitmer]
    Mark Whitmer
    May 6, 2026 05:15 pm

    Based on your earlier comment regarding “preferential treatment of PPH applicants,” I think IamI can be excused for thinking you were concerned about special treatment of PPH applications. Now it’s clear that your interest is specific to special treatment for Chinese PPH applicants. What a curiously targeted interest! I find it astounding that someone would be worried about Chinese applicants receiving cheaper accelerated examination for their applications while not being concerned about Chinese applications receiving much less US examination scrutiny based on a Chinese determination of patentability under Chinese laws. How did you come by this peculiar fixation?

  • [Avatar for Ron Katznelson]
    Ron Katznelson
    May 6, 2026 04:18 pm

    To IamI: Thanks for pointing this out.
    However, the FY2026 reduction in the count credit examiners receive for PPH applications cannot account for their substantially more favorable treatment of Chinese PPH applications compared to other PPH applications, as shown empirically.

  • [Avatar for IamI]
    IamI
    May 6, 2026 10:20 am

    Ron, the change from 2.0 to 1.5 counts for a PPH case is on the USPTO website in their FY26 PAP presentation slides.

  • [Avatar for Ron Katznelson]
    Ron Katznelson
    May 5, 2026 05:32 pm

    Jim, you raise an important point.
    Please provide evidence that examiners claim “that the USPTO is allowing significantly less examination time for PPH cases than non-PPH filings.” There is none that I am aware of.

    That said, there is circumstantial evidence that examiners are actually directed to cut corners in examining Chinese PPH applications compared to other PPH applications. For example, a PPH requirement that all the claims in the U.S. PPH application “sufficiently correspond” to the allowable claim(s) in the corresponding originating foreign office application requires comparison to the translated English version of the foreign claims. But in its “PPH 2.0,” the USPTO abandoned its duty to verify such claim compliance and instead stated in the Official Gazette that the “applicant will no longer need to submit a copy of the allowed claims from the application filed in the PPH 2.0 participating office or any English translation thereof.” 1395 Official Gazette 204 (October 15, 2013). The USPTO never explained waiving this key PPH requirement. Moreover, inspection of some file histories of PPH Chinese applications reveals that most do not submit an English translation of the prior art raised at the foreign originating office actions. As a result, USPTO examiners often allow on first action claims formulated for the US PPH application that were never allowed in the originating patent office.

    Dr. Julie Burke’s empirical study published at “USPTO’s Speed on Some China Patents Bears a Closer Look” confirms the clear preferential treatment of Chinese PPH applications compared to US-originating applications coming through the PCT.

  • [Avatar for Jim Patrick]
    Jim Patrick
    May 4, 2026 08:00 pm

    Ron,
    What are you thoughts on patent examiner claims that the USPTO is allowing significantly less examination time for PPH cases than non-PPH filings?

  • [Avatar for Ron Katznelson]
    Ron Katznelson
    May 4, 2026 04:42 pm

    To Patentwatcher,
    You state that “USPTO offers fast-track grants in some cases” and point to non-PPH patent applications that issued in less than one year. You have apparently ignored my comments, which expressly explain that the USPTO charges a fee for entering the fast-track prioritized examination (Track I), while waiving all such fees for PPH applications receiving prioritized examination. You should have checked the prosecution history of all eight OpenAI patents you linked to — they were all fast-tracked subject to the applicant having paid additional Track I fees for each one.

    The point Patentwatcher missed is that the USPTO’s unlawful preferential treatment of PPH applicants discriminates against US applicants who must pay Track I fees to obtain the same prioritized examination benefits. For example, the fact that Chinese PPH applicants receive US patents within a year compared to three years for US applicants who cannot afford the prioritized examination fees confers early exclusion power to those Chinese entities to the detriment of others in the field.

    This is particularly troubling given that the top Chinese PPH patent recipients are entities listed on the U.S. Department of Defense’s Section 1260H list of Chinese military companies. See 90 Fed. Reg. 1105 (January 7, 2025). A “Chinese military company” is defined as an entity (i) owned or controlled by, or acting as an agent of or on behalf of the People’s Liberation Army or any other component of the Central Military Commission of the Chinese Communist Party, or (ii) that is a “military-civil fusion contributor to the Chinese defense industrial base.”
    For example, just to name a few, public USPTO PPH petition records show that as of 2025, the number of US applications that issued from, or are pending in the PPH, and that are assigned to Chinese military companies include the following: 368 for Contemporary Amperex Technology Ltd. (CATL) in the area of batteries; 178 to Inspur Co. in the areas of cloud computing and big data processing; and 57 to Huawei Co. in various areas of communications and internet servers.

  • [Avatar for patentwatcher]
    patentwatcher
    May 2, 2026 01:45 am

    There is also the opposite to SAWS. USPTO offers fast-track grants in some cases. OpenAI has been granted patents within 9-10 months from filing, in addition with claims of remarkably broad scope. See https://evolve-ip.com/openais-large-language-model-llm-patents/
    Does this show another type of “weaponization” at the USPTO ?

  • [Avatar for Ron Katznelson]
    Ron Katznelson
    May 1, 2026 11:59 pm

    Gene, excellent article pointing out violations of federal law.
    Note also that Edward Martin’s letter points to another program that likely violates federal law. He states: “Because it appears that much of the unconstitutional SAWS activity favors Chinese foreign inventors, I am also interested in how the Patent Prosecution Highway (PPH) … were also weaponized to help the People’s Republic of China.” Indeed, PPH requests are dominated by Chinese applicants, as seen in the meteoric rise at the USPTO in the share of PPH applications originating from the Chinese patent office of 3,011 in 2025, compared to the second largest share from the EPO of only 476 applications. https://www.jpo.go.jp/e/toppage/pph-portal/data/requests.xlsx . China is by far the major beneficiary of the PPH at the USPTO.

    The USPTO’s PPH is likely unlawful because it grants prioritized (out-of-turn) examination while waiving the very fees that Congress mandated for that benefit. The AIA, § 11(h)(1)(A)(i) requires that a “fee of $4,800 shall be established for filing a request … for prioritized examination of a nonprovisional application for an original utility or plant patent,” leaving no discretion to exempt particular applicants. Yet the PPH provides the same accelerated treatment as Track-I examination while eliminating the prioritized examination fee, petition fee, related processing fees, and the limit of 4 independent claims, or 30 total claims.

    This is not a minor procedural variation but a direct circumvention of a substantive statutory command. By selectively removing a congressionally-imposed economic condition designed to regulate demand, the USPTO effectively substitutes its own policy judgment for that of Congress—an action beyond its authority. Moreover, the PPH fee waiver and entry structure constitute an unlawful substantive rule adopted without statutory authority or required rulemaking. The USPTO confers substantial financial benefits purportedly to “encourage greater PPH participation,” thus exercising Congress’s taxing/policymaking power by waiving a statutorily mandated fee and using that waiver to influence behavior. Because the Patent Act does not authorize substantive rulemaking and the APA requires notice-and-comment procedures for such rules, the PPH operates as an ultra vires regime that is both “not in accordance with law” and “arbitrary [and] capricious.”

  • [Avatar for Anon]
    Anon
    May 1, 2026 03:35 pm

    Yet she also confirmed that SAWS itself operated outside OPQA’s purview, saying in a declarative manner that “SAWS was not run by the Office of Patent Quality Assurance.”

    Who ran it then?

    And does this not then contradict the historical admission (when SAWS was closed down) that such WAS a quality program?

    Let alone that that admission included the statement that SAWS was only one of “such quality programs.”

    Quite clearly, actual quality needs sunlight – not shadows.

  • [Avatar for Julie Burke]
    Julie Burke
    May 1, 2026 02:07 pm

    anyone find it strange that a person who played “a significant role” in the first SAWS program is now Deputy Director of OPQA?

  • [Avatar for Pro Say]
    Pro Say
    May 1, 2026 11:44 am

    If it walks, looks like, and quacks like a shadow docket, it’s a shadow docket.

    Director Squires: Please continue your and PTO leadership’s superb, yeoman’s work on the behalf of American innovation by bringing to full light — and eliminating once and for all — these illegal shadow dockets.

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