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               COMMISSIONER'S DECISION

 

STATUTORY SUBJECT MATTER-S 2:Testing and Developing The

                           Capacity of Human Lungs

 

Following the principles of the S.C.C. in Tennessee Eastman v.

Commissioner, the process for measuring and increasing the

capacity of air sacs of human lungs lies in the field of

practical application, and is not related to medical treatment

in the strict sense or in the use of a medicine. The process

has utility in the sense that the process is controllable by

the means disclosed. The rejection was on the basis that the

process performs on a non-industrial product, that it is

essentially non-economic, and that it is dependent on

professional skills.

 

FINAL ACTION: Reversed

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This decision deals with a request for review by the Commissioner

 

of Patents of the Examiner's Final Action dated August 17, 1972

 

on application 016,962. This application was filed on April 8,

 

1968 in the name of Edward Fitz and refers to "A Device For

 

Developing The Lungs". As stated by the applicant in the

 

specification, "This application refers to a device and method

 

for increasing the capacity and strength of lungs. More

 

particularly, this invention relates to a device and method for

 

exercising the lungs and improving the capacity thereof."

 

In the prosecution terminated by the Final Action the examiner

 

rejected claims 7 and 8 in that they are directed to subject

 

matter not allowable under Section 2 of the Patent Act. Claims

 

7 and 8 read:

 

7. A method for measuring the increase in capacity and

strength of air sacs in human lungs comprising the steps

of: collecting air expelled therefrom against an

opposing force measuring the amount of air collected,

recording the amount and repeating each of the foregoing

steps.

 

8. A method in accordance with claim 7 including the steps

of varying the opposing force after each repetition of the

method.

 

In the Final Action the examiner stated in part:

 

Claims 7 and 8 are directed to a diagnostic method for

use on a living body, i.e., to diagnose the capacity and

strength of the lungs, and as such, even though the wording

of the claims calls for "measuring the increase", the method

would also indicate any "decrease" and thus in effect the

method tests or diagnoses the condition of the lungs in

terms of capacity and strength.

 

Although the present method of measuring the increase in

capacity and strength of the lungs in a human body may be

new, useful, and unobvious, it is however, not susceptible

of industrial application. The method here, which is performed

on a non-industrial product i.e., on lungs in a human body, is

rather conceived as being essentially non-economic as it does

not produce a result in any way associated with trade, commerce

or industry in the sense that those expressions have been used

in court decisions on patent applications directed to methods

dependent on professional skill. (See Lawson vs. Commissioner

of Patents, or Tennessee Eastman Co. vs. Commissioner of

Patents); the matter contained by the said method claims is

also contrary to the spirit of the expression "working in a

commercial scale", referred to in the Patent Act.

 

The applicant, in his response to the Final Action dated January

 

25, 1973, stated in part:

 

The Examiner's rejection is based on the argument that

even though the method may be new, useful and unobvious,

it is performed on a non-industrial product. This

argument is evidently based on the British line of cases

which are based on an interpretation of the British

Statute to require a vendable product. The Examiner

has referred to the Lawson and Tennessee Eastman cases,

which might be taken as implying that the principles

of the British Statute are applicable in Canada. Since

then, however, the Supreme Court of Canada has rendered

its Judgment in Tennessee Eastman Company et al vs.

Commissioner of Patents. The reasoning of the Supreme

Court makes it clear (at page 8) that a method of

surgical treatment involving the use of a substance

is not patentable, as otherwise there would be an

easy way out of the restriction as to the patentability

of substances under Section 41(1) of the Patent Act.

This ground of decision is obviously inapplicable to

the present case, as applicant is not trying to obtain

protection for a medicinal substance. Also on page 8

of the Tennessee Eastman case the Court makes it clear

that decisions dealing with the patentability of in-

ventions under the United Kingdom Act are not entitled

to the weight attributed to them by various authors in

view of the substantial differences between the British

and Canadian Statutes. Therefore as the Examiner's

objection with respect to the requirement of an industrial

product is based on the line of cases which interpret the

term "manufacture" in the British Statute, it is submitted

that the entire matter should be reconsidered. It is clear

from the decision of the Supreme Court that the claims should

not be rejected unless some basis for rejection can be found

in the Canadian Statute rather than the British Statute. We

know of no requirement in the Canadian Statute that the method

result in the production of a vendable product.

 

At the outset the Board observes that at the time the Final Action

 

conformed with Patent Office guidelines relating to the patentability

 

of inventions involving processes of testing related to the human

 

body, as distinct from processes for testing other natural products,

 

or industrial products and of materials used in the manufacture of

 

such products.

 

The examiner advanced the argument that the claims are directed to

 

a diagnostic method that is performed on a non-industrial product,

 

and that the method is essentially non-economic and does not produce

 

a result in any way associated with trade, commerce or industry in

 

the sense that those expressions have been used in court decisions on

 

patent applications directed to methods dependent on professional skill.

 

The basic issue is therefore whether the subject matter of the process

 

as claimed in claims 7 and 8 constitutes a "useful art or process"

 

(as distinct from a fine art such as that in which novelty lies solely

 

in the exercise of professional skills, or that having intellectual

 

meaning or aesthetic appeal alone), within the meaning of Section 2

 

of the Patent Act, and in the case of claims for methods of testing

 

the established criteria of utility is usually critical in determining

 

that issue.

 

Section 2 of the Patent Act reads in part:

 

"Invention" means any new and useful art, process, machine,

manufacture or composition of matter, or any new and useful

improvement in any art, process, machine, manufacture or

composition of matter.

 

The prerequisite of utility of a "useful art or process" within the

 

meaning of Section 2, may be conveniently stated, inter alia as to:

 

whether the subject matter is controllable and reproducible by the

 

means disclosed so that the desired result inevitably follows whenever

it is worked, and whether the subject matter has utility in the

 

field of practical application (as that in relation to trade,

 

commerce or industry) which is beneficial to the public.

 

Of interest in the interpretation of Section 2 of the Patent Act is

 

the Supreme Court decision in Tennessee Eastman v. Commissioner of

 

Patents dated December 19, 1972 (unreported) which concerned claims

 

directed to a method of surgical bonding of body tissues of human

 

beings; and in which the court held that the process then under

 

consideration of applying a medicine to a human being, "... is

 

clearly in the field of practical application," as opposed to a mere

 

scientific principle or abstract theorem excluded by Section 28(3)

 

of the Patent Act.

 

As previously noted the examiner raised the objection that: "Claims 7

 

and 8 are directed to a diagnostic method for use on a living body.:.."

 

However, it appears that the process refers to "measurements" and any

 

diagnosis of the results does not form part of the process. Accordingly,

 

achieving the desired result of the process does not depend on

 

professional skills.

 

In the S.C.C.'s decision Tennessee Eastman v. Commissioner, supra.

 

it was held that patents for medical treatment per se must be excluded

 

under the Patent Act in that the use of a medical substance cannot

 

be claimed by a process apart from the process of producing it, otherwise

 

there would be an easy way out of the restriction as to the patenta-

 

bility of substances under Section 41(1) of the Patent Act. However,

 

 the present claims do not fall within this prohibition, and distin-

 

 guish factually from the claims then under consideration in that no

 

 step of using a medical substance is set out in the claims.

 

The examiner also raised the objection that the method was related

 

to a non-industrial product. It is settled law, however, that the

end result of a test process is not necessarily a physical product

 

and may be tangible information only. It is also settled law that

 

if the invention is the means and not the end, the inventor is

 

entitled to a patent on the means, vide, J. Wyburn Lawson v. The

 

Commissioner of Patents (1970) 62 CPR 101 at 110.

 

Of interest with respect to a non-industrial product is the reference

 

of the S.C.C. in Tennessee Eastman v. Commissioner, supra, Re Schering

 

A.G.'s Application.(1971) RPC 337, a case dealing with a method of

 

contraception, citing the conclusion of the Patent Appeal Tribunal at

 

page 345 as follows:

 

Although, however, on a full consideration of the matter

it seems that patents for medical treatment in the strict

sense must be excluded under the present Act, the claims

the subject of the application do not appear to fall within

this prohibition and, on the law as it stands today, they

should at least at this stage in our judgement, be

allowed to proceed.... (Emphasis added by the Court)

 

The Board is therefore satisfied; (a) that the subject matter lies

 

in the field of a "useful art" and that the claims do not relate to

 

medical treatment in the strict sense or in the use of a medical

 

substance, (b) that since no professional judgement or manual

 

expertise is involved in working the process, the subject matter is

 

controllable and reproducible by the means disclosed so that the

 

desired result inevitably follows whenever it is worked, and (c)

 

that the subject matter has utility in the field of practical applic-

 

ation which can be beneficial to the public.

 

Notwithstanding the above, the Board notes that the examiner made

 

no determination of the subject matter of claims 7 and 8 in view of

 

prior art. It appears that consideration should also be given the

 

specification with respect to Section 36 and Section 38(2) of the

 

Patent Act.

 

In the circumstances, therefore, the Board is satisfied that the

 

Commissioner ought not to refuse claims 7 and 8 on the grounds

 

that the subject matter falls outside the statutory requirements

 

of Section 2 of the Patent Act and recommends that the Final

 

Action refusing claims 7 and 8 be withdrawn.

 

J.F. Hughes,

Assistant Chairman,

Patent Appeal Board.

 

I concur with the findings of the Patent Appeal Board and withdraw

 

the Final Action and return the application to the Examiner for

 

resumption of prosecution.

 

Decision accordingly,

 

A.M. Laidlaw,

Commissioner of Patents.

 

Dated in Hull, Quebec,

this 28th day of August, 1973.

 

Agent for Applicant

 

Gowling, MacTavish, Osborne & Henderson,

Ottawa.

 You are being directed to the most recent version of the statute which may not be the version considered at the time of the judgment.