By Kevin E. Noonan —
The following is part of a continuing series on how to address the
very real problems facing the U.S. Patent and Trademark Office.

A day after the day of rejoicing for inventors, patent practitioners,
examiners, and seemingly all of civilization, fair-minded people will
concede that the U.S. Patent and Trademark Office faces a daunting
task. After years of neglect – from Congress raiding the users’ fees,
an inadequate number of examiners, technology-driven increases in the
number of applications filed, and a "count" system that has not
rewarded a style of examination that encourages prosecution to a
definitive end point – the Office is facing a massive backlog of
applications without sufficient resources to process them in a timely
manner.
If the patent bar is gladdened by District Court Judge Cacheris’
decision enjoining implementation of the new rules – representing an
attempt, albeit a misguided one, on the part of the Office to address
the pendency and backlog problems – it behooves us to propose
alternatives. Patent Docs
will be posting a series of such proposals, and we invite our readers
to provide their own ideas. As they used to say in the days of the
counterculture, "if you are not part of the solution, you are part of
the problem." Patent Office management clearly thinks the patent bar
is part of the problem; it would be satisfying to prove them wrong.
Increased filing fees for continuation applications
Under the current fee regime, Patent Office filing fees can be broken down into fixed and variable, where the fixed fees are charged for every application but the variable fees are applicant-dependent. For example, the fees for a utility application containing no more than 3 independent claims and 20 total claims is made up of the basic filing fee ($310.00, 37 C.F.R. § 1.16(a)(1)), a search fee ($510.00, § 1.16(k)), and an examination fee ($210.00, § 1.16(o)); all values are for large entities, and the basic filing fee is waived if the application is filed electronically. Applicant-dependent fees include fees for filing more than 3 independent claims ($210.00 per claim, § 1.16(h)), total claims in excess of 20 ($50.00 per claim, § 1.16(i)) and a surcharge for filing multiply-dependent claims ($370.00, § 1.16(j)). The Office also charges more for extra sheets of an application ($260.00 per 50 sheets in excess of 100 total; specification, claims, abstract and drawings), a fee reduced for applications filed electronically.
Several comments received at Patent Docs have suggested that one way of handling the backlog of unexamined applications would be to charge applicants a series of increasing fees for each additional continuation or request for continued examination (RCE) filed in an application. Suggestions have included a 25% surcharge for the second continuation or RCE, a 50% surcharge for the third, a 100% surcharge for the fourth, etc. Similarly, it has been suggested that claims in excess of 25 have an additional surcharge (some suggestions are as much as $200 per claim, and double that for claims in excess of 50). The rationale is that these applications are the cause of the backlog and Patent Office burden, using (maybe even overusing if not actually abusing) Office resources that cannot be used for other (presumably more deserving) applicants, and that our capitalist system supports such a "pay-as-you-go" or "pay-for-play" approach.
The difficulty with these suggestions is that they fall into the same trap that caused (or at least encouraged) the ill-conceived Patent Office "new rules." First, they blame the applicant for years of neglect, underfunding, and mismanagement at the Office. Second, they are to be applied indiscriminately against applicants with inventions that legitimately require more than 25 claims to fully protect them. And while they are frankly intended to influence behavior, brief consideration suggests that the behavior they produce will not solve the problem. For applicants, burdensome excess claims fees will encourage multiple filings, on the same day, of the same application with claims directed towards different aspects of the invention (compositions, methods of making, methods of using, etc.). It is unlikely that the problems in the Patent Office will be solved by encouraging more applications to be filed. Examiner behavior will also be influenced; if an examiner "knows" that an invention isn’t patentable, but cannot craft an Office action that does not provoke an applicant to abandon the application or appeal the asserted rejection(s), the examiner will simply be able to continue to reject the claims until the cost of another RCE or continuation becomes too burdensome. And the examiner will be increasing fees for the Office, a behavior unlikely to be discouraged by PTO management. The experience of applicants in the biotechnology arts relating to restriction practice is indicative of the problem: during the past 10 years it has not been uncommon for the Office to issue multiple (in excess of 10) restricted groups, with a view towards reducing examiner burden and increasing divisional application filings (having claims of more restricted scope). Any policy that encourages examiners to "stick to their guns" with a negative consequence for applicants is no better than the new rules the Office promulgated on August 21st; they would put a premium on intransigence among those examiners who believe they "know something is unpatentable when they see it." This result would also be expected to increase pendency times.
Any system of increasing fees would have to protect those applicants who can least afford excessive patent filing fees. Exempting small entities is one possibility in this regard. However, it is not clear that even large corporations (like GSK) would be able to continue to pursue their applications if the fees, and the time in prosecution, increased dramatically. GSK’s strongest argument was that an applicant, any applicant large or small, has an expectation of fair and timely examination, and that this expectation (and any resulting patent) is the benefit obtained in exchange for full disclosure of the claimed invention. One of the great weaknesses in the new rules was that they frustrated this reasonable expectation, and it would be unfortunate indeed if this frustration became a part of any proposal to address the real problems the Patent Office faces.
For additional articles in the "Post-GSK" series, please see:
- "Regional Patent Offices," November 7, 2007
- "Tailoring Protection and Examination," November 6, 2007
- "Annuities," November 1, 2007

Leave a comment