Select Committee on Intergovernmental Organisations Minutes of Evidence


Examination of Witnesses (Questions 600 - 618)

MONDAY 21 APRIL 2008

Dr Gaudenz Silberschmidt

  Q600  Chairman: You talked about the struggle to get that document produced because of disagreement, but you also talked about it being very successful. Do you think people have learnt from that that the cooperation was worth it?

  Dr Silberschmidt: The cooperation with foreign affairs has significantly improved. The attention has improved especially. My colleagues in the Development Cooporation are currently at an interregnum, where the head of the Swiss Agency for Development and Cooperation has just retired and has not been replaced. Health is not well-placed, you do not even see it on the organigram. In recent discussions with colleagues in the Development Cooperation I was asked why I was in favour of a coordination unit within the Ministry of Foreign Affairs. My answer was that, while I am in favour of one coordination person for Health, I would be against five or seven people, which is what they have in Environment and Culture, where it has led to conflict between the foreign affairs and sectoral ministries. In the Development Cooporation they have one or two half posts currently and I would be in favour of seven posts. A lot of the conflict there is due to the fact that they are overwhelmed by the task and there are too few staff; they did not manage to get the funding increase where other countries, notably the UK, have been heavily increasing health funding. There I would be in favour of having a strengthening of Health and also having an interlocutor at senior level, which currently I do not have.

  Q601  Unallocated

  Q602  Lord Jay of Ewelme: Thank you very much. I just wanted to focus for a moment on the WHO's Global Outbreak Alert and Response System, which is clearly a crucial element in responding to present and future pandemics. You said in your written evidence, for which many thanks, that you thought that was working quite well—I think you actually said very well—under the International Health Regulations. But the WHO in their evidence to us said that there was "gross under-investment" in the system and that it depended on "strong, capable and transparent national systems", which are again subject to under-investment. One point that has struck us rather is their sense that there is a need for more investment in it. The point that I would be quite interested in your views on is that clearly the system is only going to work if there are effective national systems of surveillance and reporting so that the people who are at the centre know what is going on; and clearly in a number of developing countries those systems are very basic indeed, in some cases absent. I wondered if you had any comments on that aspect of it—the importance of effective national systems if the reporting system is really going to be effective.

  Dr Silberschmidt: I was commenting on the global infrastructure, that means WHO headquarters in the structure of GOARN, which is working excellently. I do not know if you have had the chance to see the Emergency Room in WHO, but it is really impressive and is working well. The IHR have really brought us into the 21st Century on what infectious disease control is. The strengths of the IHR are the fact that they are binding, they are universal around the world, it has an algorithm which does not bind them to known diseases any more but makes them relevant to all diseases independent of their origin. Personally, I was involved in mediating between the US and Iran on how to handle bioterrorism. We do not name it but it is covered. It is really broad for chemical, biological, nuclear, natural origin, deliberate origin, and we call it occurring naturally or otherwise, a diplomatic way of saying it is all covered. That is a strength. Another strength, which is quite significant for an international treaty, is it explicitly allows the use of non-state information. That means the health intelligence efforts of WHO have the legal backing and, when they find information from other sources, they can go back to the country and ask what is going on. Probably the biggest weakness is the fact that there are no resources attached to the national capacity building. That was a point you were making, which is absolutely true. It was tricky enough to have a package for the 193 Member Countries of WHO in a legally-binding instrument, so we were not able to put the capacity building and finances in the same instrument: that was too much. We have another fundamental problem there and I have tried to explain it in my evidence. Take the example of financing of pandemic influenza preparedness. A colleague from Australia has told me the same story. The Ministry of Health has a budget of billions for domestic purposes; the Ministry of Development Cooporation have their own priorities and, say, it is either a humanitarian crisis nor long-term development. But, wait a moment; we have things killing people, so we do not look at a threat that might kill people, we have enough other things. The Ministry of Defence should be about security but has a different concept of security. The sector-wise budgeting of our government means that there even it would be a win-win investment in fighting avian flu but the prevention of a flu pandemic never gets the same large resources. I would say we have the same dilemma in the capacity strengthening for the IHR/GOARN system, because it is a joint interest and it is not clearly in our Minister of Health's competence—"I do not have a mandate nor sufficient resources to invest in that". The Development Corporation sees other priorities, so why should they invest in that. One positive aspect is the fact that the international community, WHO leadership, is starting to re-focus on the health system, and the health system instead of a vertical disease-wise approach is about strengthening capacities. If you have a vertical IHR implementation approach, you plan the laboratory; but, if you do not have the health system to provide the samples, the laboratory does not help much.

  Q603  Lord Jay of Ewelme: That is a very interesting analysis. I suppose an answer is for Development Ministries to see capacity building as an essential part of their work. If they were to do that, then presumably capacity building here and the development of health systems would be as central as other aspects.

  Dr Silberschmidt: I would go deeper than that. Do you think that is feasible with the development mindset? We do not have a large ministry in our government with a global public good mindset yet. With a development logic which is appropriate for an African developing country, bottom-up approaches and working in the country, working strongly with NGOs, it is appropriate, but our governments lacks the mindset of providing global public good.

  Q604  Chairman: You mentioned the International Health Regulations, and it was suggested to us earlier that there could be a case for extending them to cover some of the animal health issues because of the tipping-over between animal health and human health. Do you have a view on that?

  Dr Silberschmidt: I think they are too young and rather need further strengthening and implementation then have a formal revision at this point. We now have to focus on implementing the International Health Regulations. It is already a record that we adopted them in 2005 and they entered into force on 16 June 2007 and are applied universally to each and every human being on the earth. That was extremely quick. I would be careful to enlarge, we should deepen. If you look down the road, we are relatively clear on who is the responsible secretariat and organisation for IHR; but, before going strongly into animal health, you would need an in-depth analysis to see if your gain in synergies is bigger or if you lose by creating new interfaces with in the functioning of IHR which will not be as important. For the time being I would be careful with opening it up.

  Q605  Lord Desai: I want to make an observation on what Lord Jay said. Even though people think of capacity building in developing countries, they do not think of health necessarily. Health for ministries in capacity building is not as high a priority, there are other things to develop, so there is a conflict there.

  Dr Silberschmidt: I would go further. I have recently had the Vice-Governor of a Chinese province coming to visit the Swiss health system and he was not asking development questions, he asked; what kind of public-private mix do we have? How do we make universal coverage of health insurance by using the private sector to make it work? I then went to my colleagues in the WHO, the World Bank and elsewhere, asking who in the world has significant capacity, an analytical capacity of emerging country health systems, and the answer is nobody. Nobody can tell you what the Indians, Chinese, Brazilians, Egyptians, Indonesians, South Africans can learn from each other's health systems. WHO and many other institutions know from developing countries' health systems. In the OECD the European Observatory on Health Systems and in academic institutions, think-tanks, we have started to create knowledge on industrialised countries, but we are still in the duel system, which is not a reality nowadays.

  Q606  Lord Howarth of Newport: The consequence of investing which is very real—there should be such investment in the generation of more trained personnel, doctors, nurses and other people who are needed in this field in the developing world—is that there will be a large haemorrhage of those very people coming back into the developed world.

  Dr Silberschmidt: The migration question will be the next big issue we are going to negotiate in WHO. In anticipation of that we have been asking the WHO and OECD jointly to do a project, which they have concluded now. One finding is the different domino effects. As I was saying earlier, Switzerland, although it does not import from developing countries, is still a player because we still import indirectly. On the other hand, there was a very clear finding that migration is not the main cause nor would its resolution be the solution to the workforce crisis in developing countries. While it is true for some specific countries that losing more than 50 per cent of their personnel is a key factor, for many other countries if we take India, the biggest exporter of doctors worldwide, it is less than ten per cent of Indian doctors going abroad, which means it is not a danger to the Indian health system. If we take the Philippines, the largest exporter of nurses, they deliberately train nurses for this situation. We are in a complex situation. Yes, there are instances where migration is crucial, but you have to look at all the push and pull factors, and basically all of our countries train too few health personnel.

  Chairman: Can we now move on to Intellectual Property Rights.

  Q607  Lord Avebury: In Paragraphs 17 and 18 of the document that you gave us to draw attention to Geneva's position as the health capital in the world, both as a centre of excellence for public and humanitarian health and as a generator of huge amounts of intellectual property from the existence of the pharmaceutical companies that are based in this country, you say that a balance has to be struck between protecting the intellectual property of those who fund and pioneer new drugs and getting those medicines that they generate to the people who need them as readily and cheaply as possible. I would like to ask you, first of all, if you have any specific suggestions as to how that balance of interest can be struck.

  Dr Silberschmidt: We have a mathematician as a Secretary of Foreign Affairs, and therefore the intellectual rigour of our drafting here was such that we deliberately did not put the balance of interests within the same objective. But Objective Nine is to improve access to essential drugs and Objective 18, where it does not say to maximise protection of intellectual property, it says "appropriate" protection.

  Q608  Lord Avebury: What does that mean?

  Dr Silberschmidt: I just comment on that because I am quoting somebody I want to introduce. Currently I am co-chairing an Expert Group together with the Deputy Director of the Swiss Office for Intellectual Property, where we have Health, Intellectual Property, Trade, Research, Development Corporation, Foreign Affairs, Human Rights, at the table to draw up a position on this issue. I learned from him that he is clearly saying, and industry hates to hear this, that even for us the maximising of protection of intellectual property is not maximising innovation, because you have too many patents hindering the collaboration that is needed for innovation. There is an optimal protection of intellectual property which gives you the most innovative output. The same applies to the big challenge of developing countries. The least developed countries are relatively easy, because there is hardly any industry claiming patents in least developed countries and there is not much of a conflict. The big challenge is, once again, in emerging economies because it starts to be a relevant market and it is the fastest growing market for the pharmaceutical industry, when you speak of the 20 per cent rich or middle class people within these countries, but at the same time you have poor people; and we have not found a system yet which accommodates both legitimate concerns. It is absolutely legitimate that the pharmaceutical industry wants to make profit if somebody is as rich as we are in India, China, Indonesia, Thailand or Brazil. On the other hand, it is unacceptable that the drugs are totally unaffordable for the poor in these countries. This is where we have a dilemma. You are asking for concrete examples, and I would be very cautious in the sense that we are in the process of moving out of the "patents are good" or "patents are bad" discussion. If you look at the draft Global Strategy and Plan of Action on Public Health Innovation and Intellectual Property, and the negotiations are going on next Monday and should conclude within the next week, it gives about 80 actions. The answer is that there is no silver bullet as to the action we have to do. It goes from basic research to strengthening health systems but over traditional medicine recognition, over capacity building for research and development in developing countries, over strengthening of regulatory capacity, fighting counterfeit drugs (in many countries more than half of the medicines are counterfeit), and over the intellectual property question. Switzerland has implemented the Doha amendments to the TRIPS Agreement on compulsory licence. It is the whole forest and, whichever tree you pick out, you have to look at individually; but you should not think that is the solution to the problem.

  Q609  Lord Avebury: There is not an algorithm that you could write which would tell you how to strike this balance? It is a qualitative process of looking at the various factors you mention, one of the most important of which obviously is the prevalence of counterfeit drugs, which I believe are spreading massively at the moment, which means that pharmaceutical companies are content to give way, for example, on the recent amendment to the TRIPS Agreement which allows for non-manufacturing countries to import under generic licences.

  Dr Silberschmidt: I would say that access to medicine is a challenge for the pharmaceutical industry as much as climate change is a challenge for the energy industry. Within the industry you find a similar kind of split, with some companies being fully aware of that being the biggest challenge for their industry and some others being closed or wanting to totally ignore the challenge. The tendency in both sectors is that the European countries are more on the progressive side than the US-based companies. There are always exceptions but that is the case. As Switzerland we are not fundamentally against compulsory licensing but that is a last resort. We are not happy with all of the compulsory licensing going on. Sometimes it attracts attention away from all the other parts of the game. What I am saying should not be understood the other way around, as attracting attention away from IP, because IP is one of the trees in that forest.

  Q610  Chairman: I have heard it argued that the pharmaceutical industry overstates the case for the amount of new drugs that come from their work alone but, in fact, a lot of the work is done by science-based hospitals and academic institutions on the public side. Would you agree with that? Or do you not think that is correct?

  Dr Silberschmidt: Overall, the system is not running perfectly in the sense that real innovative output is not as it should be, especially in view of the growing investment. Investment has been growing fast while the output has not been growing that fast or not at all. On the basic research side, you are absolutely right, basic research is much more government funded than it is pharmaceutical-industry-funded. We want to re-orient towards developing country needs but a sound basic research policy of a government is curiosity-driven, not objective-driven. You want to have the best research you can fund, we have to look for mechanisms which accommodate both aspects. An example is that colleagues from the Research Ministry, amongst others, as a consequence of that collaboration, have helped to set up the Research Centre of Global Health at the EPFL, the Technical University in Lausanne. On basic research you are right; and on applied research the very first results are now coming out of public-private partnerships, but otherwise can you tell me of any government that has ever developed a drug?

  Q611  Lord Howarth of Newport: The financial strength of the pharmaceutical companies in the West derives from long-term relationships with publicly-funded clients, publicly-funded purchasers, health services constructed in one way or another in these various countries, and that is another reason why I think the public interest has a very strong claim. I think it is a false argument for the pharmaceutical industries to say that their accountability is solely to their shareholders.

  Dr Silberschmidt: I would be careful with that argument, because they would immediately answer, "So take the US system, we earn more from private prices". They are against the government-set prices. We would not agree to abolish the European model, we have to rethink it. In the OECD we are starting to compare our systems better because, when you have a comparison basket with other countries, they know where they have to feed in the drug first to get the best price out. The private model would not be better in the sense that drug prices would tend to be higher, especially as in the US where you allow direct-to consumer advertising, which I think we are right not to allow. I would not go down the line of argument that it is because of the government-set price or government purchasing, I would rather go down the line of corporate social responsibility, because even if energy companies do not have government purchasers they bear a responsibility on climate change and climate mitigation; and, if the food companies do not have government purchasers, they have a responsibility on obesity and have to work on it.

  Q612  Lord Howarth of Newport: But the notion of corporate social responsibility recognised by the pharmaceutical industry does not seem to extend to the needs of the developing world. There is a market failure. They are not willing to invest in research to find drugs and treatments that are required distinctively in the developing world. Their interest is in supplying more affluent markets in the advanced countries?

  Dr Silberschmidt: I would say that in the last five or ten years the picture has changed. The Novartis Institute in Singapore, which is specifically on tuberculosis, is one example, GSK is another, and so on. It has started to change. On the other hand, we have to acknowledge that they can put one or two per cent of their research into pure corporate social responsibility and that means no return on their investment. Their argument is that it is a market failure, so they need government intervention; and, if we provide the market, they will do the research. We need to find mixed solutions, you cannot just say, "Do your job". Business is business, but it has to do it responsibly.

  Q613  Chairman: Does your Government or your Department put pressure on the drug industry in Switzerland? Or would you not describe it as putting pressure but would you describe it as discussing common problems?

  Dr Silberschmidt: On this issue we are discussing common problems. On the Swiss prices we put quite a lot of pressure and they do not like this, since my boss is the one setting the drug prices in Switzerland, and they do not like it when it starts to go down. We are discussing issues but it does not mean we just follow their view.

  Q614  Baroness Whitaker: This is another of these tensions which you have identified very clearly on Page 13 of your Swiss Health Foreign Policy—that trade can bring prosperity which leads to improved healthcare, but also it makes it much easier for infections to travel around the world, and you say that the WHO has made an exception in this case. We wondered if you had any other ideas. One suggestion we have heard is for international trade initiatives to have health impact assessments attached to them. Do you think there is any mileage in that? Or is there anything else we can do to bring trade into corporate social responsibility?

  Dr Silberschmidt: The quantitative health impact assessment is an interesting but very, very complex exercise. We need to learn more from health in all policy initiatives like that brought by the Finnish Presidency of the EU into our own policy. My approach would be slightly different. If you ask me what is best done with £1 million to improve health in Africa, I would train African health diplomats. There are very, few very good negotiators both in the bilateral and multilateral fields or on the recipient's side. The next step would be to link it to trade and bring them also to the table.

  Q615  Baroness Whitaker: So you would have health advocates as well as trade advocates coming from, say, Nigeria or Kenya?

  Dr Silberschmidt: If there is a free trade agreement negotiation and Nigeria, Kenya or whoever has a competent health diplomat from the Ministry of Health involved in the negotiation, the outcome will be significantly better for health.

  Q616  Baroness Whitaker: That is very interesting.

  Dr Silberschmidt: If you look at the WHO negotiations, there are very few individuals from all over the world, who have really mastered the game of health negotiations.

  Q617  Baroness Whitaker: Who should train these people? Should it be bilateral people, DFID, CIDA, that sort of thing? Is it an international responsibility?

  Dr Silberschmidt: In another objective for implementation, we have been helping the establishment of the Global Health Programme at the Graduate School of International and Development Studies here in Geneva, where we are running a summer course for the second time and are overbooked. Brazil has started a Masters programme in Health Diplomacy in the Fiocruz Foundation. There are other institutions starting. In the long run it should probably be the top diplomatic training institutions in industrialised countries plus local training. We are already discussing with a Kenyan colleague setting up in Kenya such courses locally to train people in negotiating skills. The interface between technical health work and diplomacy is tricky and then the international interface. It is tricky, but if you can train people that is the best return on investment.

  Q618  Baroness Whitaker: I know DFID does train people in negotiations at the WHO, but I do not know about this health diplomacy. Is health diplomacy for trade negotiations a new concept?

  Dr Silberschmidt: Overall it is a new concept. The course we had last summer, I think, was the first overall, and now they are starting in the US, and they have one starting in Brazil. There should be more of this.

  Chairman: If there is anything you feel you have not covered that you think we ought to hear about, please say so. If not, you can send it in later. If you are happy with that, thank you very much indeed, it has been very useful. We wish your new Department luck and good progress with the way it is heading. Thank you very much.







 
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