Tafas v. Dudas et al

Filing 235

AMICUS Brief/Memorandum in Support to Plaintiffs 135 MOTION for Summary Judgment, 133 MOTION for Summary Judgment filed by Ron D. Katznelson. (Attachments: # 1 Exhibit 1# 2 CD-Rom (See attachments added on 1/24/08 for the content of CD-Rom) (klau, ) Additional attachment(s) added on 1/24/2008 (klau, ). Modified on 1/24/2008 to edit text of attachment #2 (klau, ).

Tafas v. Dudas et al

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UNITED STATES DISTRICT COURT EASTERN DISTRICT OF VIRGINIA

Alexandria Division

TRIANTAFYLLOS TAFAS, Plaintiff,
v.

l:07cv846 (JCC/TRJ)

JON. W. DUD AS, etal.,
Defendants.

CONSOLIDATED WITH SMITHKLINE BEECHAM CORPORATION, et al., Plaintiff,
v.

l:07cvl008(JCC/TRJ)

JON.W.DUDAS,e/fli,
Defendants.

MEMORANDUM OF AMICUS CURIAE RON D. KATZNELSON

IN SUPPORT OF PLAINTIFFS MOTIONS FOR SUMMARY JUDGMENT

Ron D. Katznelson, Ph.D. Pro Se,

Encinitas, CA.
[phone]

rkatznelson(g),roadrunner.com

Brief of Amicus Curiae Ron D. Katznelson

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TABLE OF CONTENTS
1 INTEREST OF AMICUS CURIAE. 1

2

OVERVIEW

1

3

STATEMENT OF FACTS

2

4

DEFECTS IN THE ECONOMIC IMPACT ANALYSIS PROVIDED BY THE
USPTO 2

5

THE USPTO PROVIDED MISLEADING, INCOMPLETE AND ERRONEOUS INFORMATION IN ITS CERTIFICATION UNDER THE REGULATORY
FLEXIBILITY ACT 4

5.1
5.2

The USPTO improperly certified its initially Proposed Rule under the RFA
USPTO's RFA Study failed to meet its own agency guidelines for RFA

4

compliance and the Federal Information Quality Act 5.3
6

6 6

The USPTO improperly certified its New Rules under the RFA

A CREDIBLE AND EFFECTIVE ALTERNATIVE REGULATORY APPROACH WAS PROPOSED BUT SILENTLY REJECTED BY THE USPTO WITHOUT COGENT DISCUSSION IN THE FINAL NOTICE
CONCLUSION

8
12

7

ii

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TABLE OF EXHIBITS

Exhibit 1 Exhibit 2

Declaration of Dr. Ron D. Katznelson, including Appendices A - F thereto. Certification Analysis Under The Regulatory Flexibility Act, by ICF International, Published by USPTO on August 28,2007 at
(Produced by USPTO at A08270 - A08306).

h

Exhibit 3

November 25,2005 Memorandum from B. Knight to T. Sullivan regarding

Certification Under 605(b) of the Regulatory Flexibility Act, (A07325 - A07327).
Exhibit 4
Exhibit 5

August 3,2006, "Relevant Data regarding USPTO filings" (A04546 - A04553).
Department of Commerce, Guidelines For Proper Consideration Of Small Entities In Agency Rulemaking. Notice of availability at 68 Fed. Rep. 8201.

Published at http://www.ogc.doc.gov/ogc/legreg/zregs/guidelines.htm. February
20,2003.

Exhibit 6
Exhibit 7

July 10,2007, Memorandum from W. Covey to T. Sullivan regarding Certification Under 605(b) of the Regulatory Flexibility Act, (A08307 - A08315).
July 18,2006, USPTO presentation by Jay Lucas, Deputy Commissioner for Patent Examination Policy: How the New PTO Regulations Will Impact Your Practice - George Mason University School Of Law Fifth Annual Symposium On Hot Topics in Patent Law (A08960 - A08979).

Exhibit 8

July 22,2006, USPTO presentation by John Doll, Commissioner for Patents, Intellectual Property Law Summer Institute, (A08980 - A09029). April 25,2006, USPTO Town Hall Meeting on Patent Claims and Continuation Practice, Alexandria, VA, (A00253 - A00273).

Exhibit 9

Exhibits 10 - 27 Listed and referred to in Appendix E to Exhibit 1 hereto.

Ill

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INTEREST OF AMICUS CURIAE

I, Ron D. Katznelson of Encinitas, California, pro se, submits this brief as amicus curiae in

support of the Tafas and GSK plaintiffs' motions for summary judgment. I am an engineer, an
inventor, an independent entrepreneur and a user of the U.S. patent system for more than two (2)

decades. I have no financial interest in any of the parties to the current action, nor do I have any

financial relations with the law firms representing any of the parties in this action. I submit this Brief because as an inventor and co-inventor for 25 U.S. patents and pending applications, I
depend on patents and on the patent application process for protecting my inventions. I will be

directly harmed by these rules, as will many other small entities. My technology based business
prospects depend in large degree on the ability to compete and exploit my own innovations under protection provided by the patent system. My abilities to profit from my own creations and

ability to obtain investment capital to turn future inventions into useful products will be
significantly compromised under these rules.

2

OVERVIEW

Plaintiffs are seeking to permanently enjoin or otherwise vacate the United States Patent and

Trademark Office's ("USPTO") new rules on continuations and claims1 ("New Rules"). This
brief addresses only two aspects in support of Plaintiff s summary judgment motion.

The first aspect is the fundamental deficiencies of the USPTO's economic impact analysis of the New Rules and its improper certification under the Regulatory Flexibility Act ("RFA") that they

would have no significant economic impact on a substantial number of small entities.2

The

USPTO published a study in support of its certification under the RFA ("RFA Study").

Unfortunately, the RFA Study and the New Rules were not subject to public comment. The RFA Study is replete with errors and flawed analysis that renders the USPTO's certification invalid, thereby violating the RFA. In failing to correctly consider important aspects of its New Rule's
impact, the USPTO also violated the Administrative Procedure Act ("APA").

1 72 Fed.Ree. 46716. (Aug 21, 2007). 2 5 U.S.C. § 605(b).
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The second aspect discussed in this brief is the fact that alternatives to reduce USPTO workload
were proposed but silently rejected by the USPTO without a cogent discussion in the notice of

the New Rules.

The APA requires that the USPTO study, evaluate and address during the

rulemaking process and prior to promulgation of its rules, proposed alternatives to its rules for achieving its goal of reducing workload burdens.
violated the APA

The USPTO failed to do so and therefore

3

STATEMENT OF FACTS

I have submitted a supporting Declaration (Exhibit 1), including Appendices A - F thereto,

(hereinafter "Dr. Katznelson Decl.") setting forth my interest in the case, as well as factual account of certain communications I have had with USPTO officials and my submissions to the

Office of Management and Budget ("OMB").

In the interest of brevity, I beg leave to

incorporate herein by reference the factual statements in my declaration and its appendices in their entirety, to the extent that any party should subsequently elect to challenge as "material"
any of the factual matter contained therein.

4

DEFECTS IN THE ECONOMIC IMPACT ANALYSIS PROVIDED BY THE USPTO

The detailed analysis attached (Exhibit 1, Dr. Katznelson Decl., Appendix E, hereinafter

"Appendix E") shows that the USPTO's impact analysis was woefully deficient. The economic

impact analysis was provided in the USPTO's Regulatory Flexibility Act Study that it published

after the New Rules were issued, (Exhibit 2- the "RFA Study").3

The RFA Study grossly

understated the number of small entities affected by the claim limit in the New Rules

(Appendix E §3.1) by asserting that only 1% would be impacted by this rule rather than 24% to

30%, as plainly evident from the record. The RFA Study failed to identify fundamental factors
that govern the costs of preparing the Examination Support Document ("ESD") and grossly

underestimated these costs (Appendix E §3.2).

It is shown that the RFA Study's method of

3 USPTO, Certification Analysis Under The Regulatory Flexibility Act, by ICF International, (Produced
by USPTO at A08270-A08306, published no earlier than August 28, 2007 at

h .

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annualizing ESD costs is fundamentally flawed because it assumes that small entities file only

one patent application per 20 years, when in fact small patenting entities file an estimated

average of 1.2 applications per year (Appendix E §3.3). The RFA Study ignored the economic
burdens of rebutting the presumption of patently indistinct claims and assumed that such costs are zero when in fact estimates show that the average cost per small entity application filed
would be in excess of $4,200 (Appendix E §3.4).

The USPTO failed to analyze or consider other important aspects of the problem.

It ignored the

rapid rise of the fraction of applications that would be affected by the New Rules (Appendix E

§3.5.1), the disproportionate adverse impact on small entities (Appendix E §3.5.2), the disproportionate adverse impact on emerging growth industry segments (Appendix E §3.5.3) and the disproportionate adverse impact on domestic inventors, negatively affecting U.S.

competitiveness (Appendix E §3.5.4). All of these factors are important aspects of the problem
to which the USPTO was alerted during the comment period.

An agency rule must be set aside if it is "arbitrary [or] capricious." 5 U.S.C. § 706(2)(A). The

opinion in Motor Vehicle Mfrs. Ass'n v. State Farm Mut. Auto. Ins. Co., 463 U.S. 29, 43 (1983)
indicates that the failures described above are among several categories that are considered
arbitrary and capricious:

"[T]he agency must examine the relevant data and articulate a satisfactory explanation for its action including a rational connection between the facts found and the choice made. In reviewing that explanation, we must consider whether the decision was based on a consideration of the relevant factors... Normally, an agency rule would be arbitrary and capricious if the agency has relied on factors which Congress has not intended it to consider, entirely failed to consider an important aspect of the problem, offered an explanation for its decision that runs counter to the evidence before the agency, or is so implausible that it could not be ascribed to a difference
in view or the product of agency expertise. The reviewing court should not attempt itself to make

up for such deficiencies: We may not supply a reasoned basis for the agency's action that the agency itself has not given". (Citations and quotations omitted, emphasis added).

"Arbitrary and capricious" review is non-deferential when an agency has failed to "cogently

explain why it has exercised its discretion in a given manner, failed to address alternatives, or
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failed to address all relevantfactors". See Id., 463 U.S. at 47,48, and 57. (Emphasis added).

5

THE USPTO PROVIDED MISLEADING, INCOMPLETE AND ERRONEOUS INFORMATION IN ITS CERTIFICATION UNDER THE REGULATORY
FLEXIBILITY ACT.

5.1

The USPTO improperly certified its initially Proposed Rule under the RFA.

On November 25, 2005, the USPTO sent a letter to SBA Advocacy certifying under 5 U.S.C.

§ 605(b) of the Regulatory Flexibility Act ("RFA") that the proposed continuation rule

subsequently published in the Continuations Notice of Proposed Rule Making4 ("Continuations
NPRM") would not have a "significant economic impact on a substantial number of small

entities." The USPTO produced this letter in its Administrative Record, (Exhibit 3). In a related proceeding, the Examination of Claims Notice of Proposed Rulemaking was published on the

same day5 ("Claims NPRM"). However, for reasons it failed to explain, the USPTO did not
produce in its Administrative Record a similar certification letter for the Claims NPRM, although

the Federal Register notice indicates that such a letter was sent to SBA Advocacy.6

In the RFA section of the Claims NPRM7, the USPTO stated what might have been presented to
SBA Advocacy in such a letter. It stated that only 1.3% of small entities' patent applications
contain more than 10 independent claims and arrives at its certification conclusion merely on the

basis of its statistics on independent claims. But its proposed rule was not based only on the

number of independent claims.

Rather, it required applicants to designate 10 representative

claims (independent and dependent) for examination in order to avoid submitting an ESD. Therefore, contrary to the USPTO RFA statements, under the Claims NPRM, every application
submitted with more than 10 total claims would have required a submission of an ESD or

USPTO, Notice of Proposed Rule Making "Changes to Practice for Continuing Applications, Requests for Continued Examination Practice, and Applications Containing Patentably Indistinct Claims"
Jl Fed. Ree. 48. (January 3, 2006).

Patent Applications", 71 Fed. Rev. 61. (January 3, 2006).
6

USPTO, Notice of Proposed Rule Making, "Changes to Practice for the Examination of Claims in
Claims NPRM, at 66, Col. 2.
---

7 Id.

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cancellation of claims or investment in deciding which claims to designate as representative.

The USPTO failed to disclose that applications having more than 10 total claims contain an average of nearly 25 dependent claims from which to decide designation and that the top 20% of

all applications have an average of 48 dependent claims from which to decide designation8. The
USPTO misled SBA Advocacy onto a false statistical garden path of independent claims, when its RFA analysis should have disclosed that 80% of small entity applications have more than 10

total claims and therefore would be affected by the Claims NPRM.9 The USPTO chose to focus
only on independent claims, arbitrarily and capriciously concluding without any basis that the
cancellation of dependent claims is somehow "economically insignificant" or that the

designation decision time is insignificant10. Moreover, the Claims NPRM makes no mention of
any statistical data pertaining to the number of dependent claims in applications or the decision

of the USPTO to treat dependent claims as "economically insignificant" intellectual property
assets. Consequently, it denied SBA Advocacy, OMB and the public the opportunity to

scrutinize, analyze and comment on such critically relevant information and assumptions.

To the extent that the USPTO argues that its New Rules are a "logical outgrowth" of the Claims NPRM, it violated the RFA by withholding key information about the number of dependent

claims in applications and by failing to disclose and explain its criteria that dependent claims
have an insignificant economic value.

9 USPTO's memorandum, Exhibit 4, at A04550, ("Of the 154,145 nonprovisional applications field in
the first and second quarters of FY 2006, 121,905 (79%) have more than 10 total claims but only 1,664
(1.08%) have more than 10 independent [claims]").

produced by USPTO (A03554-A03620) shows that the average number of dependent claims within applications having more than 10 total claims is 24.8 and that 20% of all applications had more than 28 dependent claims wherein the average number of dependent claims over this top-end set is 47.7.

8 Calculations based on the detailed joint claim distribution in applications filed during FY 2004 as

just for making the claim designation decision, it would have had to conclude that the proposed rule must be designated as "Economically Significant" under EO 12,866 - an obligation it evaded by this omission. Evidence that USPTO knew it falsely evaded the Economically Significant designation can be found in the above-mentioned USPTO memorandum (Exhibit 4, at A04552), where the USPTO acknowledged that the economic impact of designating 10 representative claims would exceed $150M.
5

10 Had the USPTO acknowledged that 80% of all applications required applicants to perform legal work

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5.2

USPTO's RFA Study failed to meet its own agency guidelines for RFA compliance
and the Federal Information Quality Act.

The Department of Commerce, the USPTO's parent agency, has issued department - wide

guidelines for compliance with the RFA11 ("Guidelines"). Among other items, the Guidelines
direct the USPTO to compare the costs of compliance for small and large entities to determine

whether any small entities are disproportionately affected.
Guidelines then provide:

For § 605(b) certification, the

Disproportionalitv. Do the regulations place a substantial number of small entities at a significant competitive disadvantage to large entities? If the answer is "Yes," the rule should not be

certified}2 (Emphasis added).
The RFA Study failed to make such comparison in any instance. According to USPTO's own
impact criterion, the claims distribution data shows that small entities are 40% more likely than

large entities to be impacted by the claims limit of the New Rules (Appendix E §3.52).

Relying on facially wrong analysis in virtually every aspect as detailed in Appendix E, and by

not having submitted for peer review or public comment the RFA Study, the USPTO violated the

Federal Information Quality Act13 and USPTO's own guidelines for Information Quality14 as
issued thereunder.

5.3

The USPTO improperly certified its New Rules under the RFA.

From the previous section, it is clear that in essentially every category, the RFA Study

understated the economic impact of the New Rules. The analysis in Appendix E shows that

(Exhibit 5).

Of Small Entities In Agency Rulemaking, at http://www.ogc.doc.gov/ogc/legreg/zregs/guidelines.htm.

11 68 Fed. Ree. 8201 (Feb. 20, 2003), Department of Commerce, Guidelines For Proper Consideration
12 Id, at 5. 13 Pub. L. 106-554, Section 515.

Note particularly the "Objectivity" section under the "Quality" heading. ("In a scientific, or statistical context, the original or supporting data shall be generated, and the analytical results shall be developed, using sound statistical and research methods. If the results have been subject to formal, independent, external peer review, the information can generally be considered of acceptable objectivity").
6

14 USPTO, "Information Quality Guidelines," at http://www.uspto.eov/web/offices/ac/ido/infoqualitvpuide.html.

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(a) The 5/25-Claim limit rule would have a significant economic impact on a substantial
number of small patenting entities.

(b) The requirement to identify and rebut a presumption of patently - indistinct claims would have a significant economic impact on a substantial number of small patenting entities.

The RFA Study effort partakes of an artifice to feign good faith, statutory compliance. However, the USPTO did not comply with the statute and should not have certified the New Rules under
Section 605(b) of the RFA. Nevertheless, on July 10, 2007, the USPTO sent a letter to SB A

Advocacy certifying under 5 U.S.C. § 605(b) of the RFA that the New Rules would not have a

"significant economic impact on a substantial number of small entities" (Exhibit 6). The USPTO
knew that it provided incomplete and misleading information in its RFA analysis of the New

Rules.15

Moreover, it was specifically aware of the fact that even a preliminary proper

consideration of its available data on the number of total claims in applications would preclude it from an RFA certification and require it to perform the full economic regulatory impact analysis under the RFA. Based on the evidence in the record for this second certification prior to

publication of the New Rules, SBA Advocacy was not told that 24%-30% of small entity applications have more than 5/25 claims. It was told that only 1% would be affected and had no
other information that might have alerted it.

The RFA as amended in 1996 affords considerable discretion in formulating an appropriate remedy for the USPTO's failure to comply with the statute. In granting relief for a violation, a

court may take corrective action which includes remanding the rule to the agency and deferring

enforcement of the rule against small entities unless the court finds that continued enforcement
of the rule is in the public interest. 5 U.S.C. § 61 l(a)(4).

that the facts were contrary to those used to support USPTO's assertions of the minimal impact).

15 See Appendix E, at Section 2 (discussing the evidence in Exhibit 11, showing that USPTO staff knew
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A CREDIBLE AND EFFECTIVE ALTERNATIVE REGULATORY APPROACH WAS PROPOSED BUT SILENTLY REJECTED BY THE USPTO WITHOUT COGENT DISCUSSION IN THE FINAL NOTICE

The APA requires that the USPTO study, evaluate and address during the rulemaking process
and prior to promulgation of its rules, proposed alternatives to its rules for reducing its workload burdens. The USPTO was aware of specific proposals that were neither frivolous nor out of

bounds for reducing examination workload by a substantial factor and therefore had an

obligation to consider them.l6 As a member of the Trilateral Patent Office, the USPTO was
aware of procedures for Examination-On-Request or Deferred Examination by Default employed
in foreign patent offices such as those in Europe and Japan. In the last decade, the USPTO This report

participated in writing the Trilateral Patent Office's annual statistical reports.

routinely publishes information showing that under such Examination-On-Request systems, the

resulting examination rate is substantially lower than 100%. The report shows that under such

examination system, 15% to 40% of applications are never examined.17
applicants' voluntary abandonment of obsolete claims prior to examination.

This is due to

In 2004, Congress specifically authorized the USPTO under the Consolidated Appropriations

Act of 200418 to charge separately for application filing fees and examination fees, thereby
enabling USPTO's implementation of Examination-On-Request procedures. In discussing

Comment 340 in the Final Rules' text, the USPTO admitted that several parties have proposed
during the comment period that the USPTO adopt Examination-On-Request or Deferred

Examination system in order to reduce its workload. These comments suggested providing for
automatic deferral of examination, extending the period of deferral, allowing third party requests

(concluding that agency's failure to consider an alternative that was neither frivolous nor out of bounds
violated the APA).

16 Chamber of Commerce of U.S. v. Securities and Exchange Com'n, 412 F.3d 133, 145 (C.A.D.C.,2005)

http://www.trilateral.net/tsr. The examination rate details are shown in the top of table in the "Procedures" sheet in the web annex at http://www.trilateral.net/tsr/tsr 2005/web annex/web annex.xls (see the EPO and JPO examination rate and compare to the 100% shown for the USPTO).

17

Trilateral Patent Offices, Trilateral Statistical Report 2005 Edition (2006), available at

that separates user fees to permit deferred payment of examination and search fees).
8

18 Pub. L. 108^47,118 Stat. 2809 (2004). (Provides that 35 U.S.C. 41 shall be administered in a manner
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for examination of deferred applications, eliminating any negative impact on patent term
adjustment resulting from deferral, adopting deferral of examination procedures used in other

countries such as Japan and Canada, tying the period of deferral to the actual filing date of the
application rather than the claimed benefit date, and establishing deferral fees based on the

length of deferral.79 In response, the USPTO only stated: "in view of the comments received on
the deferral of examination procedure, the Office is studying whether changes (e.g., the maximum deferral period, third party request for examination, and patent term adjustment) to the

deferral of examination procedure would be appropriate".20 Clearly, the USPTO ignored the fact
that it must act on such suggestions prior to promulgating its rules. The statement that it would
consider such proposal in the future is unavailing.

There is evidence that strongly contradicts the substance of USPTO's statement in its response to
Comment 340 that it had not considered or decided on Examination-On-Request procedures and

that it will do so in the future. The USPTO had not only considered Examination-On-Request in

some detail (see presentation by Jay Lucas, Exhibit 7, at A08975 - A0897821; presentation of
John Doll, Exhibit 8, at A09003 - A09004), but has also selectively sought and received inputs on it from special interest groups in several Ex Parte meetings (Dr. Katznelson Decl. fH 3, 8-10, Appendix B). In addition, the potential benefits of an Examination-On-Request system were

quantified in public comments filed by the undersigned during the second comment period

associated with OMB's review of the New Rules (Dr. Katznelson's Decl., Appendix C).22 OMB

contemporaneously published these comments23 and the USPTO had an obligation to consider
them but omitted them from the Administrative Record.

19 New Rules at 46829 Col. 2. 20 Id.

21 See also USPTO's Jay Lucas' specific request for alternatives in Exhibit 9, at A00266, ("[USPTO is] 22 Letter from R.D. Katznelson to Susan Dudley, OIRA Administrator, dated June 29, 2007, at 20-22,
available at http://www.whitehouse.pov/omb/oira/0651/comments/460.pdf. open to alternatives that fix these [workload and pendency] problems. rather than simple complaints about these proposed solutions").

Need constructive suggestions

23 See OMB's web site at http://www.whitehouse.gov/omb/oira/0651/comments/460.html.
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In his July 22,2006 presentation, Commissioner John Doll listed the benefits of an ExaminationOn-Request system as follows:
"Expected Benefits · Non-deferred cases will be examined more quickly.

· · ·
·

The upfront cost of filing will be reduced. Delayed payment of certain fees will allow additional time for applicants to consider the
commercial viability of inventions before further expenditure of funds.

The Office can devote its time and resources to applications deemed more pressing by
applicants Pendency will be reduced because some applications will not proceed to

examination"?* (Emphasis added).
There is no question, therefore, that the USPTO was well aware of the advantages of such an examination system. The fact that the USPTO received Ex Parte responses to Deferred

Examination proposals is corroborated by remarks made in the RFA Study as follows:25.
"The USPTO continues to study whether changes (e.g., an increased deferral period, third party
request for examination, and patent term adjustment) to the deferral of examination procedure

would be appropriate, but notes that patent user groups have historically not favored increases in

the deferral of examination. Therefore, the final rule does not contain this alternative." (Emphasis
added).

The USPTO admits in the statement above that it relied on undisclosed patent user group's inputs, which were withheld from the public, to decide that it would forgo an opportunity to
reduce its workload. The potential reduction forgone would dwarf any illusory savings the

USPTO purported to have from the New Rules. Nowhere in the public record can one find the

reasons for the "patent user group" objections to deferred examination, or the reasons for the
USPTO's ceding to such purported objections despite its own recognition of the workload reduction potentials, as indicated by Commissioner Doll's statement cited above.

The reasons given to the undersigned by USPTO official Mr. Love and ex-official Mr. Spar for

the "patent user group's" objections were concerns that deferral of examination would result in

24 Exhibit 8, at A09004. See also Exhibit 7, at A08977. 25 RFA Study, note 3, at 31.
10
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loss of legal work and reduced professional fees that these "patent user groups" would otherwise
receive from their clients (Dr. Katznelson's Decl. fflj 8,9). If so, USPTO's abandonment of such
a proposal is perplexing because it should have gone forward with such a system precisely

because the "patent user group" objected to the loss of legal work ~ confirming that examiners would also see loss of burdens. Contrary to USPTO's representation in response to Comment

34025, it withheld critical information related to its consideration and decision not to adopt an
alternative procedure that goes to the heart of reducing examiner workload. This ExaminationOn-Request alternative was authorized by Congress and proposed by several parties during the

comment period. This amounts to rulemaking based on Ex Parte hidden influence of an interest group, or due to other publicly unknown reasons. The evasive and disingenuous statement in the New Rules' text suggesting that the USPTO will consider Deferred Examination in the future
makes no sense because it has already done so.

To be sure, the USPTO was not required to consider "every alternative ... conceivable by the mind of man ... regardless of how uncommon or unknown that alternative" may be. Vehicle Mfrs. Ass'n, 463 U.S. at 51, 103 S.Ct. 2856. Motor

Here, however, a specific examination

workload reduction alternative was proposed and the USPTO's own statements supported its
soundness, making it hard to see how that particular regulatory alternative was either

"uncommon or unknown."

The undocumented Ex Parte conduct in which Examination-On-

Request ideas were presented only to certain interest groups and not to the public as a whole is a
serious lapse in USPTO's responsibility to the public to address its workload problems as

provided by law. Its failure to disclose that it had considered such measures and rejected them
for unknown reasons and its obfuscation of the matter in its response to Comment 340 is a clear
violation of the APA.

26 New Rules at 46829 Col. 2.
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For the foregoing reasons, amicus curiae Ron D. Katznelson, supports the issuance of a permanent injunction against the promulgation of the New Rules.

Respectfully submitted,

Ron D. Katznelson, Ph.D.
Pro-Se

Encinitas, CA

Office: [phone]

rkatznelson@roadrunner. com

12

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CERTIFICATE OF SERVICE
I hereby certify that on this 9th day of January 2008,1 sent for filing the foregoing with the Clerk
of the Court, which upon entry will send electronic notification of such filing (NEF) to all counsel of record.

Ron D. Katznelson, Ph.D.

.T.

Encinitas, CA.

Office: [phone] rkatznelson@roadrunner. com

Brief of Amicus Curiae Ron D. Katznelson