Select Committee on Intergovernmental Organisations Minutes of Evidence


Examination of Witnesses (Questions 880 - 891)

TUESDAY 22 APRIL 2008

Mr Philippe Petit and Mr Antony Taubman

  Q880  Lord Desai: Even if I have signed the WTO and I am subject to TRIPS and whatever the patent is, it is under the old TRIPS, there is still no way of finding out whether I am subject to that patent or not as a country?

  Mr Taubman: It is ultimately possible, it is just very resource intensive. When we work with civil society on these issues, they point out that the private sector does have the resources to pay people to spend a long time going through the documents, but an NGO looking to procure drugs for their humanitarian aid does not have the resources. It is about evening up access to information. But in principle it is there, it is a public document.

  Q881  Lord Desai: I thought a patent was granted for all countries?

  Mr Taubman: No, they are strictly territorial. This is one of the major difficulties in understanding that we find. For example some key patents are in force in the US and Europe but not in many developing countries, so it is impossible to legally assert patent rights in those countries.

  Q882  Baroness Whitaker: Quite a lot of anti-malarials are fake and the WHO is concerned about this and uses the words "global public health crisis". Whose responsibility is it to deal with counterfeit medicines? Is it yours or WTO's? Is it Interpol's? If there is more than one, who is the conductor of the orchestra?

  Mr Petit: Counterfeiters are no longer isolated craftsmen, but more and more large international mafias counterfeiting medicines as well as cosmetics, agro-food products, automotive and aircraft spare parts. As far as medicines are concerned, we fully agree with WTO that the problem of counterfeit drugs is a global public health crisis. Under the aegis of WHO and the International Medical Products Anti-Counterfeiting Taskforce—IMPACT—which was created in 2006 led by WHO (and our organisation is an active participant in this taskforce with other international institutions, such as the World Customs Organisation and Interpol and other governmental and non-governmental institutions) WIPO contributes with legislative assistance, education, capacity-building and awareness-raising on this task of fighting counterfeit medicines, which are a large danger for health and sometimes for life. We have an action of capacity-building for judges, which we are the only organisation to do. Sometimes judges are not very happy to receive lessons from international organisations, but we organise seminars with some judges who are already very competent who discuss with their colleagues and train them in intellectual property matters and fighting against counterfeiting. In the framework of this IMPACT taskforce, led by WHO, there are draft principles for national legislation against counterfeit medical products, which should be approved by the next World Health Assembly in May, next month. We contribute to this with the other organisations.

  Q883  Baroness Whitaker: That is very helpful. As you see, the brief wonders if there are tensions between the work of your Advisory Committee on Enforcement and your Development Agenda. I have to say that I am not absolutely sure what tensions these might be, but maybe you can think of some tensions.

  Mr Petit: There is no tension between the work on counterfeiting and the Development Agenda. There is one recommendation, which in fact is the last of the 45 recommendations of the Development Agenda, which deals with this matter and it is taken from the terms of Article 7 of the TRIPS Agreement. It is in full accord with the TRIPS Agreement, there is no contradiction and tension. What is more important is that developing countries know that counterfeit medicines are particularly bad for them. In fact, the proportion of counterfeit drugs is higher in Africa than anywhere else.

  Q884  Baroness Whitaker: Indeed?

  Mr Petit: It is a threat to the health and lives of the population. As a consequence of counterfeiting, companies in industrialised countries may lose money but in developing countries people may lose their lives, that is the difference. Developing countries' governments are fully conscious of that. There is nothing against development in combating counterfeiting for medicines; on the contrary, it is part of it.

  Q885  Baroness Whitaker: I agree with you.

  Mr Petit: The authorities of developing countries need support to be able to control this plague.

  Q886  Lord Desai: This is about the structure of your income derived from registration fees. People say that you do not have either the resources or the incentives to deal with public interest matters and help. Is that the case? Or do you feel that is not right, not a restriction on your activities, your self-financing methods?

  Mr Petit: Well, there is no contradiction between our registration services which generate income and the rest of the activities of the organisation, which are more classical UN institution tasks contributing to the Millennium Development Goals. There is no contradiction because the mandate of WIPO in its funding convention is to promote the protection of intellectual property and also to maintain services facilitating the international protection of intellectual property and, where appropriate, providing for registration in this field and publication of data concerning this registration. That is Article 4. In fact, the international systems of patents and trademarks, managed by the organisation, are facilitating the international protection of intellectual property. Through this system it is much easier and cheaper to obtain an international patent or trademark protection. We should remind you that at the beginning the Patent Cooperation Treaty, commonly called the PCT, was not beneficial. It was supported by the contributions of the Member States, but fortunately, or unfortunately if you consider that was not the right thing, it has been a great success, and now 48 per cent of all international patents in the world go through our system. The fact is that the two systems of registration now provide more than 90 per cent of the budget of the organisation, even after a reduction of fees in the last ten years of 30 per cent and an additional reduction of five per cent in the last few weeks. The income is not growing as fast as it had been for several years during the time of the expansion of the PCT system. There are 138 country members of the PCT system and it has achieved its full development. As we have reduced the fees, the growth of income has become very, very limited every year. To be very transparent, there is a dispute between the Member States about the possible use of additional income. In the past we have had five per cent growth of income. Some Member States consider that there should not be such a growth: most of the international organisations are financed by Member States' contributions and are imposed as zero growth in their budgets. For us, nobody decides in advance what the income of the organisation will be, if we work well, we earn more. That is a problem for some who consider that instead of having an increased income we should reduce the fees so that there is no growth in income. These are industrialised countries, of course. Some other industrialised countries consider that, if there is an income growth, it should be used for improving the registration systems which generate the income. The developing countries, quite naturally, consider that an additional income is very welcome and should be used to finance more technical assistance and more cooperation for development. We could say there is no contradiction; on the contrary, developing countries are in favour of more income to be used for more technical assistance and cooperation. This is a debate which is not solved but which is for the Member States to decide. In fact, innovative sources of financing, other than Member States' contributions, are sought for by other UN institutions. Maybe WIPO has inspired some jealously by giving an example, which may explain some of the difficulties of the organisation, because it has been too successful in a way. I should also mention that developing countries are growing users of the system.

  Q887  Lord Desai: I have accessed your data system and it is very, very good.

  Mr Petit: Korea has just passed France as the fourth user of the PCT, our patent system, and China is presently seventh after the UK, but every year China's participation grows between 30 and 50 per cent, when the UK grows between three and six per cent, so I suppose in 2008 China will pass the UK as a user of the system. It shows that developing countries are not opposed to the system of financing of the organisation. There is also special financing for activities like the IGC, and you mentioned that indigenous community delegates are financed, their travel is paid, they are paid to come and participate at our meetings.

  Q888  Chairman: A final question. I am sure you are aware of the Indonesian case, where they withheld the virus because of fear of exploitation by pharmaceutical companies. What can you tell us about that? Do you think that is going to happen again? Is that going to be a perennial problem? Or is it one can we can deal with?

  Mr Taubman: I know you are pressed for time so, in that memorable phrase, here's one I prepared earlier!

  Q889  Chairman: You are giving us something to read on the plane?

  Mr Taubman: Yes, indeed.

  Q890  Chairman: That is fine.

  Mr Taubman: Some excess luggage for you! We have done an enormous amount of work on the flu question for two reasons: the first one being that it concerns the availability of vaccines for the bulk of the community, so it could not be more important; secondly, regrettably, once again, there are complex technical questions that need to be worked through. We have done that work for the WHO, having been commissioned by the WHO by the Intergovernmental Committee that is working on these questions. The basic questions, once again, filter down to what are the specific patents of concern? Is there a pattern of taking the wild flu strain and patenting it directly since there was a concern about a misappropriation of the genetic resources (a flu virus is viewed as a genetic resource, even though we want to get rid of it) is that being taken and just patented as it is; if not, then what is going on within the patent system? Then, at the other end of the pipeline, there is a question, should a pandemic hit us, what are the structures, the arrangements, for generating the vaccine that will be needed in a blinding hurry? And what resources and infrastructure are needed to respond; what patents apply to these technologies? These two questions are quite distinct, but they were conflated in the broad debate, understandably because there is a lot of passionate concern about it. What we have done is to essentially distinguish the issues and say, firstly, this is what is going on in terms of who is patenting genetic materials taken straight from the virus; and, secondly, these are the main technologies used to produce vaccines, of course using the genetic material as one input, and this is where they are held and these are the obstacles to fast-track implementation of those technologies. They are distinct issues. We have reported on that in great detail to the WHO. You would not go to WIPO, to patent lawyers, to advise you on your personal health. Equally, it is up to the WHO to work out what technologies are going to be vital for vaccine production in the future and what innovation structures are necessary to plug the genetic material from the flu virus into the vaccine innovation pipeline. It would be very foolish to ask us about what vaccine technologies are needed. We provide the factual information about what is going on in the patent system, what the legal implications are, and what the options are for the patent system. We have done a paper saying that these are the six or seven major models you could look at; it is the job of health policymakers, appropriately, to match that information to their needs.

  Q891  Chairman: Have you put that in the papers you have given us, these six or seven options?

  Mr Taubman: Yes.

  Chairman: That is very useful. Thank you very much indeed. We have kept you longer than anticipated, we are very grateful. It is a complex area and it is very helpful to have that background. As I say, you will get a transcript and do make any factual corrections you wish to pick up or, if you want to clarify or extend any information, please let us know. Thank you very much again for coming along today.






 
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