Guest guest Posted January 26, 2011 Report Share Posted January 26, 2011 Dr. Samlee Plianbangchang 19-1-2011 Regional Director World Health Organization South-East Asia Region Indraprastha Estate New Delhi-110002, India Ph: 91-11-23370804, 23370809-11 Fax: 91-11-23370197, 23379395, 23379507 Re: WHO's impact study on IP provisions in the India-EU FTA Dear Dr. Plianbangchang, I am writing on behalf of the Delhi Network of Positive People (DNP+). Our organization was founded in 1999 as a support group of people living with HIV/AIDS (PLHIV). We actively work towards universal treatment access and provide support services to the PLHIV community. We would like to draw your attention to the ongoing negotiations between Indian Government and European Commission for a free trade agreement specifically on Intellectual Property (IP) and investment that will create barriers for the production of life-saving low cost quality generic medicines. European Commission's " TRIPS-plus " demands relevant for pharmaceuticals relate to introduction of supplementary protection certificates (patent term extension) and data exclusivity. In particular, intellectual property provisions like data exclusivity would mean that multinational companies will enjoy several years of market exclusivity (monopoly) in India on even off patent medicines - with their cheaper, domestically produced generic versions not registered and available for several years. The India-EU FTA negotiations are ongoing and are now in a crucial phase with both governments publicly emphasizing that the trade agreement is likely to be concluded in the next few months. In order to stop our government from literally trading away our lives, we rely on the studies of scientists, economists, pharmacists, lawyers, intellectual property experts. We want to highlight the harmful impact of the EU-India Free Trade Agreement on access to affordable generic medicines. We know that WHO - Regional Office for South-East Asia had initiated and completed a study estimating the economic impact of the adoption of an intellectual property rights regime (IPR) on access to medicines. The study based on a model developed by WHO and PAHO focused on the impact of product patents for pharmaceuticals, patent term extension and data exclusivity on the production and availability of generic medicines in/from India. Already in our personal experience, patents in India on Cancer, HIV, hepatitis medicines are making treatment expensive for newer therapy for these diseases. Therefore this study can prove to be a very crucial tool for us in advocating about the impact of product patent regime in India and how TRIPS plus measures including data exclusivity if implemented in India may affect the lives of millions of patients in the developing world. In particular the study can play a key role in convincing Indian decision makers that the IP provisions like data exclusivity are in fact detrimental for patients in India and other developing countries. We would therefore like to request you to share the study with us and other public interest groups at the earliest. We would like to thank you in advance, Sincerely, Vikas Ahuja President Delhi Network of Positive People Quote Link to comment Share on other sites More sharing options...
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