Patentability Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What are the four requirements for granting a patent outlined by Section 1(1)?

A

A patent will only be granted for an invention that is:

  • New
  • Involves an inventive step
  • Capable of industrial application
  • Not excluded by subsections 1(2) or 1(3), or section 4A (methods of treatment or diagnosis)

**Not an exhaustive list of exclusions, and section 76A includes further exclusions for biotech inventions**

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2
Q

What are the exclusions to patentability according to Section 1(2)?

A

At least the following are not inventions for the purposes of the Act:

  • Discovery, scientific theory, or mathematical method
  • LDMA work, or any other aesthetic creation
  • Scheme, rule, or method for performing a mental act, playing a game or doing business, or a program for a computer
  • The presentation of information

only to the extent that it relates to that thing as such.

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3
Q

What are the exclusions to patentability outlined in S1(3)?

A

A patent shall not be granted for an invention the commercial exploitation of which would be contrary to public policy or morality.

“exploitation shall not be regarded as contrary to public policy or morality only because it is prohibited by any law in force in the United Kingdom”

i.e. immoral =/= illegal

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4
Q

What does Section 4A(1) exclude from patentability?

A
  • Methods of treatment of the human body or animal body by surgery or therapy
  • Methods of diagnosis practised on the human or animal body

NB

  • methods of treatment or diagnosis performed exclusively away from the body are not excluded
  • non-therapeutic treatments may be patentable
  • therapy assumes relief of a medical condition
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5
Q

How does Section 4A subsections (2)-(4) modify subsection (1)?

(1) is method of treatment or diagnosis

A
  • Substances/compositions for use in such methods allowed.
  • Use of a substance or composition in such a method is new even if substance is known in the art (1st medical use).
  • Further specific use of known substance for such a method is new if the specific use is new (2nd medical use).
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6
Q

What subject-matter is excluded from patentability by Schedule A2?

A
  • Human body, at various stages of development, and simple discovery of its elements (includes genes)
  • Processes for cloning humans
  • Processes for modifying the germ line genetic identity of humans
  • Uses of human embryos for commercial/industrial purposes
  • Processes for modifying genetic identity of animals which are likely to cause suffering without substantial medical benefit, and animals resulting from such processes
  • Any variety of animal or plant or any essentially biological process for the production of animals or plants, not being a microbiological or other technical process or the product of such a process
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7
Q

What biotechnological inventions are expressly permitted by Schedule A2?

A
  • Plant/animal varieties not limited to a particular variety
  • Elements isolated from the human body (including genes) but industrial application must be disclosed
  • Biological material isolated from its natural environment or produced by means of a technical process even if its has occurred in nature
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8
Q

How is the “state of the art” defined in Section 2(2) and (3)?

A
  • Comprises all matter made available to the public at any time before the priority date including written, oral and use
  • (For novelty only) matter in a patent or applicaiton published on/after the priority date if:
    • matter was in the application both as filed and published
    • the priority date is earlier

NB:

  • abstract not part of the art
  • only documents which can become GB patents are citable as s.2(3) art
  • includes applications whose publication was prevented under s.22
  • if applicaiton not validly published (withdrawn too late to prevent publication) it won’t be s.2(3)

An invention shall be taken to be new if it does not form part of the state of the art

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9
Q

Can EP applications be cited as s.2(3) prior art?

A

Yes, after Dec 2007 all states (including GB) are designated by default

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10
Q

Can a lapsed PCT application be cited as s2(3) prior art?

A

No, PCT application can only be cited once they have entered the GB national phase

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11
Q

What are the conditions set out for the six month grace period in Section 2(4)?

A
  1. Disclosure due to invention being obtained by anyone unlawfully or in breach of confidence:
    1. from the inventor, or anyone in confidence of the inventor, or anyone who obtained it from the inventor because they thought they were entitled.
    2. from anyone told in cofidence by anyone mentioned in 1.
  2. Disclosure made in breach of confidence by anyone holding the invention in confidence or to whom it was disclosed in confidence (includes inventor?)
  3. Disclosure due to display at an officially recognised international exhibition, provided application states this on filing and evidence is supplied within 4 months.

NB for a discloure so be a proper disclosure, it must be enabled

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12
Q

When should confirmatory evidence be filed for a disclosure at an International Exhibition?

A

File application within 6 months

File declaration on filing

File confirmatory evidence within 4 months from filing of a GB application or 2 months for a PCT(GB) application (inform PCT receiving office on filing)

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13
Q

When is an “air of confidence” considered to be present for a disclosure in breach of confidence?

A

If, at the time that the information is imparted or acquired, the recipient understands that the information is confidential

  • Unlikely if a document is forgotten and left somewhere carelessly
  • Consider if an NDA in in place
  • Was the document marked “confidential” or password protected?
  • Employees have obligation of confidence to their employer
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14
Q

How does priority affect a breach of confidence

A

A priority claim does not mean that the breach of confidence will be disregarded for the newer application.

If there is a breach - file a PCT application immediately.

Every applicaiton, regardless of priority claim must be filed within 6 months of the breach or else the disclosure will become prior art.

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15
Q

What is the inventive step requirement of Section 3?

A

An invention shall be taken to involve an inventive step if it is not obvious to a person skilled in the art, having regard to any matter which forms part of the state of the art by virtue only of section 2(2) above (and disregarding section 2(3) above).

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16
Q

What is the industral applicability requirement of Section 4?

A

an invention shall be taken to be capable of industrial application if it can be made or used in any kind of industry, including agriculture.

17
Q

What inventions are specifically permitted by Section 4A?

A

Substances and compositions for use (i.e. medical use claims)

First and subsequent medical use claims permitted

18
Q

How is “treatment” understood in Section 4A?

A

In general:

  • ‘of the human or animal body
  • relief of a cause or symptom of a medical condition
  • purely cosmetic treatments are not considered therapeutic (so generally excluded, but consider any incidental therapeutic effect)
  • is supervision of a physician needed?
19
Q

How is ‘surgery’ defined in Section 4A?

A
  • ‘non-insignificant intentional physical intervention’ (not necessarily invasive)
  • encompasses both therapeutic and cosmetic surgery (case law leans toward therapeutic though)
20
Q

How is ‘therapy’ defined for Section 4A?

A
  • corrective/preventative/alleviates a medical condition
  • addresses a symptom or the cause
  • includes pest control
21
Q

What is the test for exclusions under section 1(2)?

A

Exclusions are limited to where the invention relates to those things ‘as such’. The current test is set out in Aerotel:

i. properly construe the claim
ii. identify the actual contribution
iii. ask if this falls solely within an exclusion
iv. (Check if the actual contribution is technical)

22
Q

What is the doctorine of equivalents

A
  1. Notwithstanding that it is not within the literal meaning of the relevant claim(s) of the patent, does the variant achieve substantially the same result in substantially the same way as the invention, ie the inventive concept revealed by the patent?”
  2. “Would it be obvious to the person skilled in the art, reading the patent at the priority date, but knowing that the variant achieves substantially the same result as the invention, that it does so in substantially the same way as the invention?”
  3. “Would such a reader of the patent have concluded that the patentee nonetheless intended that strict compliance with the literal meaning of the relevant claim(s) of the patent was an essential requirement of the invention?
23
Q

What is the pozzoli test for inventive step?

A

(1)(a) Identify the notional “person skilled in the art” – i.e. consider who would be the idealised expert in the technological field of the invention;

(1)(b) Identify the relevant common general knowledge of that person – i.e. consider what knowledge and skills that person would have to make them competent in the technological field of the invention;

(2) Identify the inventive concept of the claim in question – i.e. identify the “core” or “essence” of the invention as claimed;

(3) Identify what, if any, differences exist between the cited “prior art” and the identified inventive concept – i.e. set out the differences between the invention as claimed and the alleged current state of technology in the field of the invention (typically established based on the results of a search for prior art carried out by the UKIPO);

(4) Viewed without any knowledge of the alleged invention as claimed, do those differences constitute steps which would have been obvious to the person skilled in the art or do they require any degree of invention?

24
Q

What is the definition of “as such” as used in S.1(2)?

Exclusions

A

The current process for determining whether a claim is related to an excluded category as such is laid out in Aerotel/Macrossan [2006] EWCA Civ 1371 and Aerotel [2007] R.P.C.7:

i) properly construe the claim
ii) identify the actual contribution
iii) ask if this falls solely within an exclusion
iv) check if the actual contribution is technical.