From the ‘EPO Boards of Appeal and Key Decisions’ conference of 8-9 October 2014
‘Late Requests’, based on a presentation by Mr Hugo Meinders (Chairman of Board of Appeal 3.2.07)
This was about implementation of Articles 12(2), 12(4), 13(1) and 13(3) of the Rules of Procedures of the Boards of Appeal
• According to Art.
12(2) the parties should file their complete case at the first exchange. The
Board has the power not to admit in the appeal proceedings requests which could
have been presented or were not admitted
in the first instance proceedings.
• According to Art.
13(1) any amendment to a party’s case after it has filed its grounds of appeal
or reply may be admitted and considered at the Board’s discretion. The
discretion shall be exercised in view of inter alia:
~ the
complexity of the new subject-matter submitted,
~ the
current state of the proceedings and
~ the
need for procedural economy.
• According to Art.
13(3), anything filed after issue of the summons is not admitted if it cannot
be dealt with by the Board or the party without adjournment of the proceedings.
Although the way late filed requests are handled may vary from one Board of Appeal
to another, the political will to increase the productivity of the Boards of
Appeal may have far reaching consequences for the users of the system. Thus,
although not mentioned by Mr Meinders, the Boards of Appeal seem to show a
desire to act more as a pure second instance reviewing the correctness of the
first instance decision.
From a Report of a Meeting of the Committee on Biotechnological Inventions
Stem Cells
The latest opinion from the CJEU in C364/13 suggests that “parthenotes” are not embryos and therefore are not excluded from patentability. In addition T2221/10 appears to follow the EPO’s current practice, namely that cases filed before publication date of the single blastoma extraction process (SBP) are not patentable.
Medical use claims
T1780/12 concerned the difference in scope between Swiss style and EPC 2000 claims.
There is some concern by doctors, for example in Switzerland, that they may infringe the EPC 2000 format medical use claims. There is also concern regarding infringement for off label marketing. We think that there are differences in scope, because Swiss style claims require the manufacture of a medicament: at a very basic level are two different types of claims have different wording. There is a suggestion that EPC 2000 medical use claims might cover the use of an intermediate in a pharmaceutical formulation which then is metabolized to an active ingredient in the body. That probably would not be covered by a Swiss style claim.
No comments:
Post a Comment