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QualPharma December 2020

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PATENT AND TRADEMARK

Post grant opposition

The provisions of section 25(2) of the

Indian Patent (Amendment) Act 2005

governs the filing of a post grant opposition

by any ‘person interested’ after the

grant of the patent but before the expiry

of a period of one year from the date of

publication of grant of the patent, by way

of notice of opposition made in form 7

and sent to the controller in duplicate.

The Opposition may be made on any of

the grounds disclosed in section 25(2).

The "person interested" as per section 2

(1)(t) is defined as including a person

engaged in, or in promoting, research in

the same field as that to which the invention

relates.

On receiving the notice of opposition, the

controller constitutes an opposition

board, comprising three members, where

one of them is a chairman. The opposition

board conducts the examination of

the notice of opposition and the documents

filed under rules 57 to 60 and submit

its recommendations to the controller

within three months. Further a hearing is

scheduled between both parties by the

controller and decision for the patent to

be revoked, maintained

or amended is

taken.

It is to be noted that

the pre-grant opposition

under section 25

(1) is wider than the

post-grant opposition

under section 25(2),

as the latter allows

only ‘person interested’

to file the representation.

The

grounds of opposition for both the pre

grant and post grant oppositions are

similar.

Both Pre grant and Post grant opposition

can be made on the grounds listed below:

Wrongfully obtaining the invention

Anticipation by prior publication

Anticipation by prior date, prior

claiming in India

Prior public knowledge or public use

in India

Obviousness and lack of inventive

step

Non patentable subject matter

Insufficiency of description of the

invention

Non-disclosure of information as per

the requirement or providing materially

false information by an applicant

Patent application not filed within 12

months of filing the first application

in a convention country

Nondisclosure/ wrong mention of

source of biological material. Invention

anticipated with regard to traditional

knowledge of any community,

anywhere in the world.

QualPharma *Dec 2020* , Vol.3 ISSUE 12

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