USTR’s implausible claim that ACTA Article 1.2 is an all purpose loophole, and the ramifications if true

The October 2010 version of the ACTA text is inconsistent with several areas of U.S. law, and proposals for new laws in the areas of the reform of patent damages and access to orphaned copyrighted works. In particular, the obligations in the ACTA text do not incorporate many of the areas of limitations and exceptions to remedies found in U.S. law, and in the statutes of some other countries.

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WIPO releases program for ‘Global Meeting on Emerging Copyright Licensing Modalities’

In advance of the 21st session of the WIPO Standing Committee on Copyright and Related Rights (SCCR 21), WIPO is holding a Global Meeting on Emerging Copyright Licensing Modalities on 4-5 November 2010 in Geneva which endeavors to facilitate ‘Access to Culture in the Digital Age’. The program for this Global Meeting can be found here: http://www.wipo.int/meetings/en/2010/wipo_cr_lic_ge_10/program.html.

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Statement of the Holy See at 48th WIPO General Assembly

48th Series of Meetings of the World Intellectual Property Organization’s General Assemblies

Statement by H.E. Archbishop Silvano M. Tomasi, Permanent Representative of the Holy See to the United Nations and Other International Organizations in Geneva

at the 48th Series of Meetings of the World Intellectual Property Organization’s General Assemblies

Geneva, 21 September 2010

Mr. President,

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Access to Orphan Works, and ACTA provisions on damages

Access to Orphan Works, and ACTA provisions on damages
KEI Policy Brief 2010: 1
20 October 2010

Introduction

Copyright is a term that in the United States describes the laws that regulate the use and distribution of “original works of authorship.” The types of activities and expressions protected by copyright have expanded over the years, particularly due to technology, but also due to the lobbying by various interested parties. The current systems of registration of copyrighted works in the United includes the following catagories:

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Response by FDA to KEI’s FOIA Request Regarding the PSM India Summit of May 11, 2010 in New Delhi

In June of 2010, KEI was informed that representatives from the the United States Food and Drug Administration (FDA) had recently attended a summit in India on the issue of counterfeited and spurious medicines organized by the Partnership for Safe Medicines (PSM), a US-based organization with clear links to pharmaceutical corporate interests.

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