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Introduction to claims
Part of patent specification Heart and soul of an invention Defines the metes and bounds of an invention
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conferred protection Protection on what is claimed Allows for easy infringement analysis
Preamble
Transition phrase Body
A gel composition for treatment of pain comprising; 2-10 percent by weight Benzocaine and atleast one of propylene glycol and glycerine as a cosolvent.
Preamble A gel composition for treatment of pain Transition Phrase comprising Body 2-10 percent by weight Benzocaine and at least one of propylene glycol and glycerine as a co-
solvent.
Claim elements
2-10 percent by weight Benzocaine
Propylene glycol or Glycerine
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Introduces the invention It sets out the basic class of the invention Remove ambiguity as far as possible
Example 1. apparatus for shaking articles to dislodge impurities comprising... 2. apparatus for shaking articles to dislodge impurities, the apparatus comprising...
It recites the elements that define the invention Describes how these elements structurally, physically or functionally co-operate with each other to make the invention or how the elements should be interconnected All the unnecessary elements should be removed which will limit the claim
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Independent
Stand on their own E.g. - A gel composition for treatment of pain comprising
Dependant
Depend on another claim The gel as claimed in claim 1, wherein .... Advantage Clarifies the independent claim language claim differentiation Stand after a possible invalidity of the base claim
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Product claim
New chemical entity Claimed generally by structure or name A compound of general formula X Considered superior claim type
unless important E.g. Claim 1 - A process for treating the surface of a polyethylene article to increase its receptivity to a printing ink, which comprises
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Markush claim
Eugene Markush the first inventor to use it successfully in a US
Patent application. An alternative to writing or in claims selected from the group consisting of A, B, and C. define alternative chemical ingredients - have a common property useful in the combination claimed
E.g. Claim 1 - A process for treating the surface of a
polyethylene article to increase its receptivity to a printing ink, which comprises: exposing the surface of the article to a saturated solution of sodium dichromate in an acid selected from the group consisting of concentrated sulfuric, nitric and phosphoric acids.
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than by the process by which it was made Product to be novel and non-obvious Disadvantageous in comparison to product claims
Infringement product and process; Invalidate - product
Omnibus claim
Involves giving a reference to the description or the
drawings without stating explicitly any technical features "An x as shown in Figure y Not allowed in US Not allowable, unless absolutely necessary (Europe) No legal basis - desirable to avoid (India) described in the specification with reference to the accompanying drawings
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substance or composition "Use of substance X in the manufacture of a medicament for the treatment of condition Y EPO Swiss type claim format no longer acceptable
"A product X for the treatment of disease Y"
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Intrinsic factors
Specification
Prosecution history
Extrinsic factors
Dictionary Encyclopaedia
Expert testimony
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"The court must properly interpret the claims, because an improper claim construction may distort the infringement and validity analyses."
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PATENT
A gel composition for treatment of pain comprising; 2-10 % by weight Benzocaine in atleast in part as the free base; and atleast one of propylene glycol and glycerine as a solvent.
PRODUCT
A gel for treating neuropathies causing pain at a site by inducing analgesia. The gel is administered intradermally. The gel has 10 % by weight of Benzocaine and glycerine as solvent.
Infringing?
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element by element
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PATENT
A gel composition for treatment of pain comprising; 2-10 % by weight Benzocaine in atleast in part as the free base; and atleast one of propylene glycol and glycerine as a solvent.
PRODUCT
A gel for treating neuropathies causing pain at a site by inducing analgesia. The gel is administered intradermally. The gel has 10 % by weight of Benzocaine and glycerine as solvent.
Infringing?
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PATENT
PRODUCT
In substance equivalent
if the infringing goods are made with the same
object in view which is obtained by the patented product, then a minor variation does not mean that there is no infringement. A person is guilty of infringement if he makes what is in substance the equivalent of the patented article - Raj Prakash Vs. Mangat Ram (1977)
theory that, if two devices do the same work in substantially the same way and accomplish substantially the same result, they are the same, even though they differ in name, form or shape. - Graver Tank & Mfg. Co. V. Linde Air Products Co. Copyright 2012, Intellecture
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The differences between the accused product or process and the claimed invention must be "insubstantial."
The range of equivalents granted under the doctrine cannot extend so far as to ensnare that which was publicly done before the "prior art.
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The patentee cannot recapture subject matter relinquished during the application process (under the doctrine of prosecution history estoppel). PHE bars application of DOE
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Facts
a filtering process for the purification of a dye solution Amendment by patentee (pH 6-9) Alleged infringing process (pH 5) Infringement under Doctrine of equivalents ?
decides based on purpose Patent holder unable to establish purpose estoppel applies
Hilton Davis v. Warner Jenkinson case
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Patent
heating the resulting batter-coated dough to a
Product
Dough is heated at a temperature at 400 F.
Infringement?
Case - Chef America V. Lamb Weston
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Claim 1. A hydrosol which comprises solid particles of a cyclosporin and a stabilizer which maintains the size distribution of said particles
Product is in the form of a capsule that contains cyclosporin dissolved in a small amount of ethanol instead of water. Hydrosol formation, when ingested Infringing?
Novartis Pharmaceuticals Corp. v. Eon Labs Mfg. 363 F.3d 1306 (Fed.Cir., 2004)
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Broad definition
a dispersion of solid particles in aqueous colloidal
Limited definition
medicinal preparation formed outside the body.
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US
1, 8 and 9
1. Aqueous formulation, comprising moxifloxacin hydrochloride and sodium chloride. 8. A method of treating or preventing a disease comprising administering to a host in need thereof an effective amount of an aqueous solution ... 9. A combination preparation comprising an aqueous solution of moxifloxacin hydrochloride and an aqueous solution comprising sodium chloride...
Patents referred:
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US
1, 4, 22 and 24
Europe
1, 4, 24 (corresponding
India
4 (including limitations)
Patents referred:
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The infringer should have a great difficulty in designing around the claims. Clearly define claim terms in the specification.
Be cautious when responding to Examination reports Include claim types based on the countries of interest
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