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1. COMPETITION - McCarthy Tétrault

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EDP Operators may only provide such services to financial institutions,<br />

PFS , UCIs or pension funds set up under Luxembourg or foreign laws.<br />

Pursuant to the New Law, EDP Operators will have, amongst other<br />

obligations, to obtain a license from the Ministry of Finance and to justify a<br />

share capital of at least one million and five hundred thousand euro.<br />

For more information visit:<br />

http://www.etat.lu/legilux/DOCUMENTS_PDF/MEMORIAL/memorial/a/200<br />

3/a1121408.pdf<br />

or contact: LE_GOUEFF@vocats.com<br />

8. INTELLECTUAL PROPERTY<br />

BRAZIL<br />

LEGAL PROTECTION FOR SOFTWARE<br />

On 30th June 2003, a decision of the 3rd Panel of Superior Court in<br />

Special Appeal No. 443.119/RJ extended to software the same protection<br />

that the law previously afforded to other intellectual works. The notable<br />

case marks the first time that the highest court recognized the<br />

copyrightable nature of software, which had already been expressly<br />

granted under Law 9609/98 (the "Software Law"). This decision is also<br />

notable for the penalty assessed - the infringer was penalized with<br />

damages in an amount equal to 3,000 copies of the counterfeit product.<br />

The Copyright Law provides for this amount of damages whenever<br />

identifying the number of counterfeit copies would be impossible task.<br />

For more information please contact: rapdecunto@pinheironeto.com.br<br />

EU<br />

REGULATION ON ENFORCEMENT OF<br />

INTELLECTUAL PROPERTY RIGHTS<br />

On 30th January 2003, the Council of the European Union proposed a<br />

regulation on the enforcement of intellectual property rights.<br />

The proposed directive (the "Directive") concerns customs action against<br />

goods that are suspected of infringing intellectual property rights. The vote<br />

on this Directive has been delayed to November because of the European<br />

Institution. The European Parliament member responsible for guiding the<br />

proposal has not yet produced the report on the draft legislation.<br />

Criticism of the proposal is significant, which is being compared to a<br />

controversial U.S. law. On the one hand, the Directive has drawn<br />

dismayed reaction from copyright holder lobbyists, in particular from the<br />

International Federation of the Phonographic Industry (the "IFPI").<br />

Copyright holders seek alternative measures by which to develop the<br />

regulation. They argue that more than 1 billion pirated music CDs have<br />

been sold; thus, where one in every three CDs is illegal, the IFPI has lost<br />

$4.6 billion due to piracy. Conversely, such large earning potential has<br />

garnered support for the Directive from certain large high-tech companies,<br />

such as Microsoft.<br />

On the other hand, civil liberties groups criticize the Directive on the<br />

ground that it poses a threat to civil liberties, innovation and competition<br />

policy.<br />

According to critics, large multinationals stand to reap the greatest benefit<br />

from such enforcement of intellectual property rights. Indeed, the Directive<br />

bans reverse engineering practice. Moreover, an analysis of the Directive's<br />

implementation predicts that the law would both damage European<br />

scientific research and limit consumers' rights.<br />

Finally, although the Directive permits modification of the patentability of<br />

computer-implemented inventions, according to computer scientists and<br />

developers, it would increase the grip of multinational companies on the<br />

software industry.<br />

For more information please contact: LE_GOUEFF@vocats.com<br />

INDIA<br />

INDIA GRANTS FIRST EXCLUSIVE<br />

MARKETING RIGHTS<br />

On 5th September 2003, India's Controller General of Patents, Designs<br />

and Trade Marks granted the first ever exclusive marketing right (the<br />

"EMR") in India to United Phosphorous for sale of its fungicide, which is<br />

sold under the brand "SAAF." The few applications, which were filed earlier<br />

by various companies, were not approved by the Controller on various<br />

grounds.<br />

EMR entitles the EMR holder to have the exclusive right by himself, his<br />

agents, or licensees to sell or distribute in India the article or the substance<br />

on and from the date of approval granted by the Controller for a period of<br />

five years or until the date of grant or rejection of patent application,<br />

whichever is earlier.<br />

The provisions for the grant of EMR were introduced in the Patents Act,<br />

1970 by the Patents (Amendment) Act, 1999, to bring the Patents Act,<br />

1970 in compliance with Agreement on Trade Related Aspects of<br />

Intellectual Property Rights (the "TRIPS"). TRIPS required insertion of<br />

EMR provisions with effect from 1st January 1995 pending introduction of<br />

the product patent regime in the developing countries. The product patent<br />

regime is scheduled to come into effect on 1st January 2005.<br />

EMRs can be granted with respect to substances intended for use or<br />

capable for being used as medicine or drug. However, no EMR can be<br />

granted with respect to chemical substances that are ordinarily used as<br />

intermediates in the preparation or manufacture of any of the medicines or<br />

substances.<br />

Under the amendment of 1999, Patent Offices are required to accept the<br />

product patent applications and keep them in what is known as the "Black<br />

Box" until 1st January 2005, when such applications will be examined for<br />

the grant of patent. In the meantime, the applicant can apply to obtain an<br />

EMR, which is granted if the following requirements are satisfied:<br />

For inventions made in India or outside of India if:<br />

• before filing an Indian application, applicant has filed an application for<br />

the same invention in a convention country on or after 1st January<br />

1995;<br />

• the approval to sell or distribute the article or substance in the basis of<br />

appropriate test conducted on or after 1st January 1995 is granted in<br />

such convention country; and<br />

• applicant has received the approval to sell or distribute the article from<br />

the authority specified in this behalf by the Central Government.<br />

For inventions made in India:<br />

• before filing an Indian application, applicant has filed an application on<br />

or after 1st January 1995 for method or process of manufacture for<br />

that invention relating to identical article or substance and has been<br />

granted the patent on such application; and<br />

• applicant has received the approval to sell or distribute the article from<br />

the authority specified in this behalf by the Central Government.<br />

ISSUE 22 SEPTEMBER – OCTOBER 2003 6

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