Sunday, November 23, 2008
More on the USPTO v. Tafas & GSK Appeal
USPTO v. Tafas & GSK Appeal - Dec. 5, 2008
14 November 2008
By Gene Quinn
The United States Patent & Trademark Office appeal of the Tafas and
GlaxoSmithKline case regarding the claims and continuations rules that
were famously enjoined by Judge Cacheris of the Eastern District of
Virginia is set for oral arguments on Friday, December 5, 2008, at 10am.
I will be in attendance at the hearing and blogging immediately thereafter
with my thoughts on the hearing, providing my perspective and insights,
that is assuming there is an oral argument that day at all. I know it is
scheduled for then, but let me be perfectly open and honest about my
intentions.
I want to see the Patent Office and/or the Department of Justice step
in and do the right thing and withdraw the rules and moot the appeal. That
is the only responsible thing to do and the fact that those making the
decision to move forward with this case have not seen fit to save
themselves this embarrassment demonstrates that they are out of touch and
simply don't care what damage will be done to not only the Patent Office
but all Administrative Agencies. It is irresponsible and reckless to do
anything other than withdraw the rules, and we all need to do whatever we
can to bring pressure to bear in the coming weeks to get our government to
do what is obviously the right.
The fact that this case has gone this far is an unfortunate testament
to the fact that the Patent Office and the Department of Justice are
hell-bent on forcing the Federal Circuit to issue a decision that is
going to be nearly ruinous for all of the agencies of the Federal
government. How is it possible that a lame duck administration at the
tail end of its time in office can continue to push and appeal a case
where the outcome is so certain? This is going to be a disaster for all
agencies, and a decision that should be made by the next leaders of the
Patent Office and the Department of Justice. The claims and continuations
rules should be withdrawn and this appeal mooted. That is the only
responsible thing to do, so please Mr. Dudas, on the way out do the right
thing here and don't risk the decision of the Eastern District of
Virginia being ratified by a Court of Appeals and thus becoming
precedent that will allow for the challenge of virtually any
administrative rulemaking decision.
On Tuesday, August 19, 2008, the United States Court of Appeals for
the Federal Circuit issued a decision in Cooper v. Dudas, which makes it
clear what the outcome of the PTO appeal of the GSK & Tafas case will be.
As I pointed out in my post titled Trouble Ahead for the PTO, the Cooper
v. Dudas case, although a win for the PTO, laid the foundation for the
Federal Circuit to ratify the decision of Judge Cacheris lock, stock and
barrel. In this decision the Federal Circuit explained that the PTO does
not have the authority to make substantive rules, explained that
substantive rules are those that effect a change in existing law or
policy that will affect individual rights and obligations. The Federal
Circuit went on to explain that in the Cooper v. Dudas case the PTO was
fine because they were merely setting a working definition of an
ambiguous term used in a statute. That is hardly the case in the
Tafas & GSK appeal. The statute is clear, inventors have the right to
file as many claims as they want and file as many continuations as they
want. There is nothing in the language of the statute that supports
any limitation, and what the Patent Office tried to do clearly and
unambiguously was affecting substantive rights. Changing rules in the
middle of an application process cannot be characterized any other way.
You had the right to do something yesterday, no right to do it today.
That is a change, and it impacted a lot of pending applications.
It should not come as a surprise to anyone that the Federal Circuit
might signal in decisions leading up to an important case which way they
are leaning. They do this all the time. In fact, if the Patent Office and
the Department of Justice actually force the Federal Circuit to issue a
decision you can expect that the decision will cite the Cooper v. Dudas
opinion liberally. They have inched the law closer to where it needs to be
to support what it is that they are about to do without it being viewed
as a shift in the law. It is rare that the Federal Circuit so abruptly
changes course like they did in Bilski without moving that direction
slowly.
So I predict that if the Federal Circuit issues a decision it will be
to affirm Judge Cacheris. Now why would the Patent Office and/or the
Department of Justice want a Court of Appeals to affirm a decision that
is such an indictment of Patent Office rulemaking? I have no idea. It is
reckless and is something that should be stopped. Someone in the
government, whether in the DOJ, Department of Commerce or Congress, needs
to step in and be the voice of reason. We all know there are a lot of
needless and irrational challenges to actions taken by Administrative
Agencies, and while this is not one of those meritless situations, an
indictment of rulemaking that will flow from a Federal Circuit decision
will do nothing more than embolden challenges and flood the court system
with cases that will for years require district courts and the regional
Courts of Appeals to set the appropriate balance. The only way that will
happen is by further indictment of the Patent Office as judge after
judge explains just how bad the Patent Office rulemaking was and that
in whatever case is before them the clear disregard for the law shown by
the Patent Office is not what is at issue.
When the Federal Circuit ultimately issues its decision after the new
PTO administration is in place the claims and continuations rules will be
once and for all thrown out and there will be no doubt left that the
Patent Office did not have the authority to directly contradict the patent
laws enacted by Congress. The truth is that the Patent Office tried to
do something they didn't have the right to do and they were challenged,
thankfully, by Dr. Tafas and GlaxoSmithKline and the many amici who filed
briefs explaining exactly how and why the rules were bad and not supported
by the law. Why do our lame duck political leaders want to turn a clearly
bad decision to act contrary to the overwhelming weight of public comment
and contrary to the Patent Act itself into a miserable precedent that will
undoubtedly embolden legions of challenges to legitimately rulemaking?
Because if you continue down that path this is exactly what will happen,
and someone needs to point that out to our leaders and get them to
accept reality.
About the Author:
Gene Quinn is a US patent attorney and the founder of IPWatchdog.com, and
is the Editor and chief contributor to the PLI Patent Practice Center and
is on the PLI Patent Bar Review faculty.
This library has all the port numbers and error codes
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