We routinely provide information on IP topics of critical importance to our
clients.
AS OF JANUARY 1, 2004
- NEW U.S. PTO FEE SCHEDULE EFFECTIVE
- The U.S. PTO is amending the rules of practice to conform them to
certain amendments made to the Regulations under the Patent
Cooperation Treaty (PCT).
New FY2004 Fee Schedule is effective as of
January 1, 2004.
- IMPORTANT CHANGES TO PCT SYSTEM
- The World Intellectual Property Organization published in
the
PCT Newsletter No. 11/2003 (November 2003) the details of
very important changes that affect the procedure for filing
international applications as from 1 January 2004.
- The Newsletter No. 11/2003 provides details on:
-
- New time limit for filing the demand
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- Signature requirements
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- Changes in payment of fees
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- Requirements regarding the indication of the applicant’s address,
nationality and residence
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- Indications regarding parent application, grant or continuation or
continuation in part
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- Option of power of attorney waivers by PCT Offices, PCT
Authorities and/or the International Bureau
-
- Enhanced international search and preliminary examination system
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- Modified Request and Demand Forms
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- New edition of the Request form PCT/RO/101 which should be used
for all international applications filed on or after 1 January 2004.
- Please note that an individual designation of states and exclusion
of elections of States no longer possible.

- December 2003
On Dec. 24, 2004, U.S. PTO postponed the implementation of
the electronic filing requirements related to the Madrid
Protocol until Nov. 2, 2004 because of technical difficulties in
implementing the TEAS system. Should the TEAS forms be posted during
the extension, applicants making Madrid Protocol submissions should
use forms provided by the International Bureau of the WIPO.
- October 2003
- U.S. PTO announces a five-point plan designed to
improve the quality and consistency of restriction practices in the
examination of biotechnology patent applications. U.S. PTO also
promises to have the entire plan in place within 6 to 9 months. This
"5-point" action plan will (1) publish examples of claim sets, (2)
emphasize rejoinder practice, (3) publish and deliver restriction
practice training to all biotech examiners , (4) enhance the quality
review of restriction requirements, and (5) assess the progress of the
action plan. U.S. PTO promised to have the plan in place within 6-9
months.
- September 2003
-
European Parliament votes for exclusion of
software from patentability:"
Data processing is not a field of technology and innovations
in the field of data processing are not inventions in the sense of
patent law".
- August 2003
- U.S. PTO waives the requirement that applicants
submit copies of each U.S. patent and each U.S. patent application
publication cited in Information Disclosure Statements (IDS). The PTO
did not waive the requirement that applicants provide
copies of all foreign patent documents and non-patent literature
references. This waiver applies only to all applications filed after
June 30, 2003.
- July 2003
- U.S. PTO Adopts New Amendment Format:
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- (Original): Claim filed with the application.
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- (Currently Amended): Claim being amended in the current amendment
document.
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- (Canceled): Claim deleted from the application.
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- (Withdrawn): Claim still in the application, but in a non-elected
status.
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- (Previously Presented): Claim added or amended in an earlier
amendment document.
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- (New): Claim being added in the current amendment document.
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- (Not Entered): Claim presented in a previous amendment document
but which has either not been entered or the status of entry is
unknown to applicant when a subsequent amendment to the claims is
filed.
- June 2003
- U.S. PTO eliminates altogether the CPA practice under Rule
53(d) for utility patent applications. Further prosecution of
claims that have been finally rejected will be possible only
upon the filing of a Request for Continued Examination (RCE) under
Rule 114 or a “new” application under Rule 53(b). The “Not Entered”
identifier shall be used in a subsequent Amendment to identify “new
claims” that were filed in a previous Amendment but not entered by the
Examiner. The CPA practice continues to be maintained with respect to
design patent applications.

Below is the list of the
recent decisions in patent cases rendered by the U.S. Court of Appeals
for the Federal Circuit. Summaries that provide an in-depth description
and analysis of the impact of new case decisions or laws, the potential
implication for our clients and our foreign partners, and some practical
tips for ensuring compliance are in the Extranet area (Log-in required).
Application of the doctrine of waiver in appeals from the
Board
In re Watts, __ F.3d__ (Fed.Cir.2004)
The line of cases which are helpful in understanding other
recent decisions by the Federal Circuit on the written description
requirement
In re Curtis, __ F.3d___ , 69 U.S.P.B.2d 1274 (Fed.Cir.2004)
Amgen Inc. v. Hoechst Marion Roussel , 314 F.3d 1313, 1330
(Fed.Cir.2003)
Claim construction
Medichem, S.A. v. Rolabo, S.L., 353 F.3d 928, 69 U.S.P.Q.2d 1283
(Fed.Cir.2003)
Kumar v. Ovonic Battery Co., Inc., 351 F.3d 1364, 69 U.S.P.Q.2d 1220
(Fed.Cir.2003)
Ferguson Beauregard/Logic Controls v. Mega systems, LLC, 350 F.3d
1327, 69 U.S.P.Q.2d 1001 (Fed.Cir. 2003)
Genzyme Corp. v. Transkaryotic Therapies, Inc., 346 F.3d 1094, 68
U.S.P.Q.2d 1596 (Fed.Cir.2003)
Amgen Inc. v. Hoechst Marion Roussel , 314 F.3d 1313, 1330
(Fed.Cir.2003)
Abbott Laboratories v. Novopharm Ltd., 323 F.3d 1324, 66 U.S.P.Q.2d
1200 (Fed.Cir.2003) (Patentee is his or her own lexicographer)
Obviousness determination (overlapping ranges)
In re Peterson, 315 F.3d 1325, 65 U.S.P.Q.2d 1379 (Fed.Cir.2003)
Means-plus- function patent claim limitation
ACTV, INc. v. Walt Disney Co., 346 F.3d 1082, 68 U.S.P.Q.2d 1516
(Fed.Cir.2003)
On sale bar cases
Lacks Industries, Inc. v. McKechnie Vehicle Components USA, Inc.,
322 F.3d 1335, 66 U.S.P.Q.2d 1083(Fed.Cir.2003)
35 U.S.C. 112, 6th paragraph
Northrop Grumman Corp. v. Intel Corp., 325 F.3d 1346, 66 U.S.P.Q.2d
1341(Fed.Cir.2003)
Doctrine of equivalents
Boehringer Ingelheim Vetmedica, Inc. v. Schering-Plough Corp., 320
F.3d 1339, 65 U.S.P.Q.2d 1961(Fed.Cir.2003)
Post-Festo II cases (Doctrine of Equivalents,
prosecution history estoppel, narrowing amendments))
Smithkline Beecham Corp. v. Excel Pharmaceuticals, Inc., __ F.3d __
(Fed.Cir.2004)
Glaxo Wellcome, Inc. v. Impax Laboratories, Inc., __ F.3d __
(Fed.Cir.2004)
Deering Precision Instruments, L.L.C. v. Vector Distribution
Systems, Inc.347 F.3d 1314, 68 U.S.P.Q.2d 1716 (Fed.Cir.2003)
The line of cases dealing with the "ordinary observer" and the
"point of novelty" tests in the design patent context
Unique Functional Products, Inc. v. Mastercraft Boat Co., Inc., (Fed.Cir.,
Nov 18, 2003)(unpublished)
Catalina Lighting, Inc. v. Lamps Plus, Inc., 295 F.3d 1277, 63
U.S.P.Q.2d 1545 (Fed.Cir.2002)
Contessa Food Products Inc v. Congara Inc. 282 F.3d 1370, 62
U.S.P.Q.2d 1065 (Fed.Cir.2002)
Requirement of Cross-Referencing Related Patent Applications
During Prosecution Before the U.S. PTO
Dayco Prods., Inc. v. Total Containment, Inc., 329 F.3d 1358, 1368
(Fed.Cir.2003)
Licensing agreements
Fieldturf, Inc. v. Southwest Recreational Industries, Inc., __ F.3d
__ (Fed.Cir.2004)
The full text of many of these
opinions is available from Edward Bennett Williams Law Library of the
Georgetown University Law Center at:
http://www.ll.georgetown.edu/federal/judicial/cafed.cfm.
Our Clients can access all the opinions in
Client Extranet area.

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"...To promote the progress of science and useful arts,
by securing for limited times to authors and inventors the exclusive
right to their respective writings and discoveries.--" The Constitution
of the United States of America
Article1, Section8, Clause 8.