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WHO Perspective on Medicine Patents and FTAs

WHO Perspective on Medicine Patents and FTAs. Asian Regional Workshop on FTAs 26-28 August, 2005, Kuala Lumpur, Malaysia Dr Zafar Mirza Regional Adviser, Essential Drugs & Biologicals East Mediterranean Regional Office - Egypt World Health Organization. Outline.

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WHO Perspective on Medicine Patents and FTAs

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  1. WHO Perspective on Medicine Patents and FTAs Asian Regional Workshop on FTAs 26-28 August, 2005, Kuala Lumpur, Malaysia Dr Zafar Mirza Regional Adviser, Essential Drugs & Biologicals East Mediterranean Regional Office - Egypt World Health Organization

  2. Outline  WHO Perspective on Medicine Patents • How we view FTAs in this connection? • Existing work & plans in this area

  3. WHO Perspective on Medicine PatentsRights based approach Health is a basic human right and access to medicines is a part of this right.

  4. WHO Perspective on Medicine PatentsOur Goal in Medicines To help save lives and improve health by ensuring the quality, efficacy, safety and rational use of medicines, including traditional medicines, and by promoting equitable and sustainable access to essential medicines, particularly for the poor and disadvantaged - Up to half of the population in developing countries do not have reliable access to medicines.

  5. WHO Perspective on Medicine PatentsThe Tragedy Citizens continue to suffer and die for lack of access to essential medicines.

  6. WHO Perspective on Medicine PatentsThe Challenge 1. Unaffordable medicine prices 2. Irrational Use of medicines 3. Unfair health financing mechanisms 4. Unreliable medicines supply 5. The quality of medicines 6. New medicines are needed

  7. New drugs are to be developed, but even if they are developed would they be accessible to the poor ? New drugs for existing neglected diseases New drugs to replace ineffective or unsafe drugs New drugs for newly emerging diseases • 95% investments in R&D are for 20% people • 1% drugs in last 25 years for tropical diseases and TB, makes 11% GBD • Vaccines for HIV/AIDS, treatment of hepatitis B, Cystic fibrosis are needed • More effective drugs need to be developed for HIV/AIDS • TB, Malaria have become drug resistant to existing drugs • Safer drugs are needed to replace toxic treatments • More than 20 diseases have emerged in last 10 to15 years e.g. ebola virus; new strains of Cholera; SARS etc • All these new diseases require new treatments to be developed

  8. WHO Perspective on Medicine Patents • Essential drugs are not simply another commodity. • Patent protection has been an effective incentive for research and development for new drugs, BUT Patents should be managed in an impartial way, protecting the interests of the patent-holder, as well as safeguarding public health principles.

  9. WHO Perspective on Medicine Patents • Introduction of a public health perspective into the intellectual property protection regime • Use of the flexibility permitted by the Agreement in the revision of national laws and regulations (e.g. Bolar provision, compulsory licensing, exceptions to exclusive rights, extension of the transitional period) • Implementation of the Doha Declaration • Caution with "TRIPS-plus" provisions • Monitoring of the health impact of new trade agreements

  10. WHO Perspective on Medicine PatentsW H A Resolutions WHA52.19 May 1999 … monitoring and analysing the pharmaceutical and public health implications of relevant international agreements, including trade agreements, … to maximise the positive and mitigate the negative impact of those agreements … WHA55.14, 2002 …ensure that WHO's Medicines Strategy address … the impact of international trade agreements on access to Medicines WHA56.27, 2003 …to consider, whenever necessary, adapting national legislation in order to use to the full the flexibilities contained in the TRIPS Agreement

  11. How we veiw FTAs in this connection? • These have a long history which goes much beyond WTO. • It is a sovereign right of the countries. • States have to balance the costs and benefits (not just in economic terms) • In case of IPRs and medicines, we think that not only any TRIPS-plus approach should be avoided but TRIPS flexibilities should be fully incorporated in FTAs.

  12. WHO Perspective on Medicine PatentsW H A 57.14 (22 May 2004)Scaling up treatment and care within coordinated and comprehensive response to HIV/AIDS Urges Member States, as a matter of proiority …to encourage that bilateral trade agreements take into account the flexibilities contained in the WTO TRIPS Agreement and recognized by the Doha Ministerial Declaration on the TRIPS Agreement and Public Health

  13. What does TRIPS-Plus means in the context of FTAs? • Data exclusivity • Extension of patent term • Restrictions on use of compulsory license • Linking patents with registration

  14. Existing Work & Plans 1 • Policy development • Globalization, Trade & Health • WTO Agreements and Public Health • IPRs and Access to Medicines • Commission on Intellectual Property Rights, Innovation and Public Health • Publications; briefs; representations; meetings etc.

  15. Existing Work & Plans 2 • Technical assistance in implementation • Transitional periods • Accession process • TRIPS compliance • Legal reviews and amendments • Assistance in use of TRIPS flexibilities and safeguards • Inter-agency work

  16. Existing Work & Plans 3 • Impact assessment • Research • Methodologies development • TRIPS Network

  17. Existing Work & Plans FTAs • Technical Assistance during FTA negotiations – e.g. Andean countries • Case-study development • Policy Guide development

  18. Countries Support on IPR & Medicine issues more than 60 countries

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