Select Committee on Intergovernmental Organisations Minutes of Evidence


Examination of Witnesses (Questions 1019 - 1039)

TUESDAY 20 MAY 2008

Dr Iain Gillespie and Dr Benedicte Callan

  Q1019  Chairman: Good morning, Dr Gillespie and Dr Callan. Can I first of all thank you very much for your time today. As you know, we are a Select Committee of the House of Lords looking at the question of intergovernmental organisations and contagious diseases. The main issue is the way the intergovernmental organisations work together and, of course, the non-governmental organisations that link in with them. Although to do that we obviously need to have some sort of knowledge about those diseases, the main purpose is the interaction between the non-governmental organisations, intergovernmental organisations and the value that the British Government gets out of the taxpayers' money that we put into it. Today's proceedings are being recorded, but you will have an opportunity to see that before it is published and to do any corrections of factual matters. If anything occurs to you after this session that you feel was missed out or needs to be elaborated, please feel free to contact us and tell us. Please feel free for either of you to chip in on the questions as we go along. We want to get as much information as possible, that is the purpose of this hearing, so do not feel inhibited in that respect. Perhaps it would be helpful if you could start by just telling us a little about your two respective roles.

  Dr Gillespie: Certainly. I will begin. Good morning. Thank you very much indeed for making the time to take oral evidence from us. It is a pleasure to do this in English as well. From my side it is a strange accent in English and from Benedicte's side even a more different accent in English. As you know, the OECD is an economics organisation focused on economic development and driving globalisation and free trade. Perhaps I could say something very briefly about how the organisation approaches its work on health and infectious diseases. In general there are three areas that we focus on across the OECD. There is our own area, which is innovation. We come from the Directorate for Science Technology and Industry. We both sit in a division called the Biotechnology Division, which is perhaps something of a misnomer because essentially what this division does is try to look at how the life sciences can drive growth and transition structural change through innovation. Other parts of the organisation with a role are particularly our Development Assistance Committee which, as you know, is very focused on aid architecture, our Development Centre which looks at issues such as sustainable financing for development and, not least, our Health Committee which focuses on health system performance and health systems efficiency. We also host a couple of important processes which are not formally part of the OECD but they address issues around global health. One is the Africa Partnership Forum, which exists to help OECD countries engage in the NEPAD Agenda, and the second is the Heiligendamm process support unit which is a dialogue between the G8 countries and the so-called O5 countries, which are Brazil, India, China, South Africa and—

  Q1020  Chairman: Mexico.

  Dr Gillespie: Mexico, thank you. The Heiligendamm process is looking at IP and innovation as one of its lines. That is where we sit in the organisation. As I say, we come from the innovation side.

  Q1021  Chairman: Thank you very much indeed. Can I, then, perhaps start by asking you about this question which has come up a number of times about the co-ordination between the vertical and the horizontal as it has been referred to, which I am sure you are familiar with. The general view, which I know you take from the evidence I have seen of yours, is that a functioning health system in a country is absolutely vital. There is a lot of emphasis put on the vertical treatment of disease, particularly by some of the NGOs. We have had various arguments put to us saying that these two are not as contradictory as they seem and, in fact, they are more angles than horizontal or vertical. I would like your view on that, and I would like your view particularly on where Noordwijk, if I have pronounced that correctly, fits in on this. Could you start with that, both the horizontal and vertical—is that right, is it a sensible distinction, and how does it fit into the Noordwijk Agenda?

  Dr Gillespie: Let me begin and I will probably pass for specific comments on Noordwijk to Benedicte. Thinking about horizontal and vertical approaches, that is a perfectly reasonable holistic device to look at the various initiatives that are going on but, for us, there is no right way. The right way is not horizontal, the right way is not vertical, it has to be a mixture of both. Where we saw intervention in global health starting was very much on the so-called vertical axis, although, in fact, it was only partly a vertical axis; what we saw was a focus on getting products for AIDS, TB and Malaria to patients. The focus was, if you like, at the far end of the vertical part of looking at individual diseases. There was very little work done on the upstream R&D for any of these diseases. That seems to us a very reasonable place to have begun but where we are now, of course, is that we are looking for horizontality across the entirety of the system, first in functioning healthcare systems in recipient countries where we have some limited progress still, secondly in horizontality and systems efficiency, systems complementarity, across the various vertical initiatives, and, thirdly, around the innovation system itself, where focus has tended in the last few years to be on elements of the system, in particular on developing molecules for particular diseases. We see a more systems-based approach across the entirety of the innovation cycle in R&D to be a long-term, much more efficient way. In short, vertical and horizontal are both required but, in our view, what is really required is a much more holistic and effective systems approach to the development of innovation and the delivery of these innovations in recipient countries. As to Noordwijk, I think that was very much the starting point for our thinking, but perhaps I can ask Benedicte to say a little bit more about the specifics.

  Dr Callan: Just to add to what Iain was saying, in Noordwijk, although it was a joint collaboration between those parts of the OECD that focus on innovation and heath issues and those parts of the OECD that focus on aid and development assistance, there was a strong focus on what can be done to change the innovation system as a whole in order to meet the needs of the developing world. There was a focus on two complementary sets of issues. One, what can we do to increase the innovation system efficiency as a whole, and really there was a tension with some groups saying, "We have got to focus in on a few diseases", and others saying that rather we need to look at the set of incentive mechanisms and infrastructure needs that can lead to a more efficient innovation system. The second issue that was dealt with in Noordwijk was how do you build capacity, both in OECD countries for R&D in this field and capacity in the developing world for R&D. You are right to say that the OECD focus has been very much more on this horizontal aspect, and I think that our colleagues in DCD would agree that their present focus is more on health system capacity. That said, as you put it earlier, we do not want to give the impression that the vertical programmes have no value, they are of great value, and in R&D it is going to be almost impossible to construct an innovations system where there is not a disease-by-disease based approach to the improvement of research and research capacity in those areas. Our focus really was on the more general innovation system dysfunctions.

  Q1022  Chairman: Thank you. Dr Gillespie, you mentioned that you have looked at requiring holistic outcome, and one can understand that is an ideal thing to aim at, but, given the disparities between various countries on their basic health systems, I suppose the brute question is: where do you start?

  Dr Gillespie: I think the pragmatic answer to that is that you start from where you are now. We have a whole range of interventions in place, a whole range of initiatives. The majority of them, as you said, are vertical, but that does not mean that efforts cannot be made to make these vertical initiatives actually stack up together to reduce some of the transaction costs in delivering the outputs of these systems and try to make the systems support one another. As you are very well aware, this is part of the real goal of the Paris Declaration on Aid Effectiveness on the delivery side. Equally, one wants to provide interventions, whether it be drugs, vaccines or whatever, into a system which have some absorptive capacity for these materials. That requires a more horizontal approach on actually developing healthcare systems. One size, of course, will not fit all. What Country A requires will not be what Country B requires. Equally, within the innovation systems, as Benedicte has said, we see disease-specific innovation, but at least in the upstream parts of R&D we feel that there are some structural issues that can be developed which can improve the efficiency of innovation. You are right, there is no one-size-fits-all for each of the different countries which have very different health requirements, but thinking about uniting, if you like, bringing together, reinforcing, the synergies across these vertical systems, for us at least is a key element in this notion of horizontality.

  Dr Callan: Can I just add to that. Our DAC colleagues would say one of the most important elements of any programme that is going to help build health systems and strengthen health system efficiency is going to be a line-up of country plans. They would push very strongly for ownership and alignment by recipient countries of any programme that is designed to help improve their health systems. That is one of the areas where their position would be that you really have to start with the recipient countries and see what they feel their own health system needs are.

  Chairman: Thank you. This leads us on quite neatly to co-ordination, which Lord Howarth will ask about.

  Q1023  Lord Howarth of Newport: Could I ask you about governance, who does what in this already very complex scene, and what the value is that OECD in particular adds in a scene where there are already a great many intergovernmental organisations and groupings of one sort or another, a very crowded architecture? In your submission you said: "the OECD is well-placed to play a role in taking action forward ... " with reference to improving innovation and access to medicines, "not least since it is able to draw together the key players (governmental, non-governmental, industry, researchers and civil society) in developing innovation systems and in delivering innovation". Two questions arise from that. Do you have the executive power at OECD to drive this process internationally? And would it not be the responsibility of the World Health Organisation? Is that because perhaps it simply has not been very good at it or because it is not an appropriate role for it?

  Dr Gillespie: Let me start off by saying there can be no doubt as far as any of the OECD countries are concerned that the intergovernmental organisation, that leads in these areas, is the World Health Organisation. The issue of innovation in public health is under discussion now, as we sit here, in the World Health Assembly in Geneva. We certainly hope, and I think I can speak not just for the two of us but for all of our colleagues in the OECD, indeed for all of our member countries, that there will be an effective resolution coming out of the World Health Assembly to strengthen WHO's mandate and capacity in looking at innovation for global health. Let me say that upfront. Secondly, you asked the question: does the OECD have executive power. The work programme and the priorities of the OECD are set by our Council, the 30 member countries, through their executive committee. At the moment they are paused and they have paused following our Noordwijk meeting waiting for the World Health Assembly to take a decision on where WHO should be going on the innovation and public health agenda. It is not for me to say what they will do next, it is for them to decide what the OECD may do next, but it is very clear that whatever the OECD does next on the innovation and global health agenda that will be aimed to complement and support what WHO take forward coming out of the strategy that we are hoping is adopted at the World Health Assembly. This is a role that we see the organisation of the OECD increasingly looking to play, if you like, providing some of the analytical capability to supplement and support work that is going on across other parts of the IGO architecture. As far as the point about the OECD's convening powers, there are some aspects around innovation that the OECD currently has a longer track record on and more substantive capacity at present than the WHO has, and that would be something I would expect our interlocutors in the WHO to advocate as much as we do. What we see ourselves doing next, if the OECD Council decides that this is appropriate, would be to work with the WHO, partly to help them build their capacity but, frankly, more simply to bring some of the analysis that we have been doing around innovation efficiency in the delivery of health technology into their debate. This is something that we have formulated in a Memorandum of Understanding, a formal document between WHO and the OECD. We hope that we will continue to operate that partnership, we will strengthen it in the field of innovation and health over the coming years.

  Q1024  Chairman: Dr Callan?

  Dr Callan: I would just jump in and echo some of the points, but perhaps give a little bit more detail in the areas where the OECD has capacity that the WHO may not have worked quite so much in. First of all, as you mentioned, we have a whole division that does mapping, measuring and analysis of innovation systems, how they function, what are the policy tools to spur innovation, what is the substitutability of these different policy levers, whether they are complementary. There is a whole range of work that the OECD has done that is of relevance to this field of infectious diseases and has not been applied to infectious diseases but could easily be done if that was something that our member countries felt was necessary. In the DAC, the issue of how you align and make more effective overseas development systems is a big issue. They are taking the issue of global health as one of their primary areas of concern. The measurement and approved effectiveness of health systems is something that the community on health works on in collaboration with the WHO and they share both their methodologies and the data that they generate. For some countries this is a very important area; for others, it is more controversial. On this issue of policy effectiveness and policy coherence, the OECD has worked very strongly on how you create coherence between different policy fields in finance, health, development, science and technology, and how you create a larger vision of what your overarching policy goals are. Those are specific areas where the OECD has experience and a secretariat that could apply its expertise to the issue of global health should countries feel that was something that was absolutely necessary. More specifically, and this gets back to the Noordwijk Medicines Agenda, what was suggested in very politically nuanced terms, because it was a text that was negotiated amongst a large group of different individuals and organisations, was the OECD has work on open innovation models, collaborative mechanisms for IP. Those are things we have been working on for our own countries and looking at their applicability: when they are useful and why they are useful. This is something that has been taken up by the WHO as something that is important and should be pushed forward. We have experience in why these models work, why they often are hard to put in place, and that is something the two organisations need to work together to push forward. Innovative financing mechanisms for R&D, as I mentioned earlier, is something that the WHO is interested in and I think that is what they are going to be pushing forward as the first elements of work following this WHO resolution if my understanding is correct. Again, there is an awful lot of work on policy levers for achieving certain scientific goals or industrial goals. The OECD has certain capacity where we could collaborate more closely. I would perhaps mention as a corollary to that these alternative mechanisms to improve innovations that we have been working on. There are very specific things where there is possibility for more collaborative work but there are also some very overarching large general areas where the OECD perhaps has a history of work that might be useful.

  Q1025  Lord Howarth of Newport: So the answer to the question as to what value OECD is adding in this field of international health is that you are analysing and reporting on such issues as the failure to innovate and on coherence and collaboration. Is anybody else doing that kind of work?

  Dr Gillespie: On the work looking at collaboration and development of research networks involving individuals from the bottom up, at the international level I think it is fair to say that the OECD maintains, if you like, a substantial lead. This is an area which WHO, through their Intergovernmental Working Group on Public Health, Innovation and IPs, has said is important, but so far they are only beginning to dip their toes in the water. This focus on how you drive innovation efficiency, whether it be in health or other areas, is something which the OECD has a substantial lead in. In fact, this is the core of our new OECD Innovation Strategy launched by our ministers last year that we report back to ministers in 2010 on.

  Q1026  Lord Howarth of Newport: So what is the bridge from analysis to action? You report?

  Dr Gillespie: Yes.

  Q1027  Lord Howarth of Newport: How are the implications of your reports taken forward? Is there some mechanism that exists or that you would desire should exist?

  Dr Gillespie: It depends very much on the specific output that we are looking for. Like any other organisation we have a panoply of tools at our disposal. Sometimes what we will do is analysis and policy reporting where essentially what we are looking for are the actors who are involved in the analysis and reporting. I should just say in parenthesis here that the actors involved are from member countries, member country governments, plus from the NGOs, from a number of non-member country governments and also from the innovative industry. The process of analysis and development of reports which are agreed by the actors has an impact on diffusion. What we are essentially trying to do is move some novel means of thinking. There is an adage in the OECD that says you can get anything done in the OECD as long as someone else takes the credit for it!

  Q1028  Lord Howarth of Newport: Should that be the WHO? Is the WHO the lead organisation internationally for carrying forward the implications of the research that you carry out?

  Dr Gillespie: It is one of the lead organisations. First of all, I should say there is analysis, but we also have a number of soft law mechanisms in place, governance frameworks, that allow or encourage our governments and the private sector to act in certain ways. Is the WHO the principal customer of analysis in this area? I would say it is one. The WHO has some executive power. Some of the recommendations are aimed very much at member country governments themselves. Some are aimed at the practitioner at the ground level and that practitioner may be a researcher in a university, it may be a pharmaceutical company, a biotech company or a product development partnership. The strength of the analysis is the fact that we try to internalise in that analysis all of the different actors and their perspectives, and it is the bottom-up approach to development of policy directions that we think is a critical strength of the approach that we bring to bear.

  Q1029  Baroness Hooper: I suppose that the WHO has the lead in the sense that it is a truly global organisation in membership terms. I was just wondering whether the fact that the OECD is an expanding organisation has any impact on your work. I know Brazil is a recent new member with a very important and large economy and, of course, you have a new boss.

  Dr Gillespie: Secretary General.

  Q1030  Baroness Hooper: From Mexico. Does that help you with your work in terms of the follow-up that Lord Howarth has been talking about? I imagine it does. The second thing, if I may, is that I am a member of the Parliamentary Assembly of the Council of Europe and we do an annual report on the OECD which is coming up at the next session in June and we always try to focus on some health issues and educational issues as well as the general economic background. Is that helpful to you? Maybe we could concentrate more in terms of follow-up on asking questions about what is happening once the analysis has been done and the follow-up is due to take place.

  Dr Gillespie: I think they are both very helpful questions, if I may say so. We do, indeed, have a relatively new Secretary-General, Mr Angel Gurria, from Mexico. One of the core missions that he was elected upon was to make the OECD a more relevant organisation as a hub of globalisation looking much more outwards than perhaps we have hitherto. We have entered into discussions with five member countries to join the organisation and a further five so-called "enhanced engagement" countries, looking to build them into the work of the organisation without becoming full members. These include countries such as Brazil, China, India, Russia, Indonesia and a number of other key countries. That outward-looking face of the OECD must be helpful in the interaction with the follow-up to these kinds of global initiatives. Having said that, for some time we have had quite a lot of activity with non-member countries. If we look at the OECD in this area, our members still account for about 65 per cent of GDP but 90 per cent of global R&D. One of the real motivating factors for trying to play a role in this issue around innovation for global health is that most of the innovation, most of the R&D and most of the spend is in the OECD countries; so, if you like, we have a special responsibility for driving innovation to meet the needs of the majority of the world. That was very much the basis for our debate in Noordwijk. If you have a chance to look at the agenda, you will see there was quite a range of very senior players from non-member countries there as well. As far as the Council of Europe is concerned, by happenstance tomorrow we have a discussion with the Education and Science Committee in preparation for the Parliamentary Assembly's debate. One of the things that we will be raising in that discussion will be our work on infectious diseases. It will also cover issues like genetics and genomics, GMOs, human data banks, et cetera. As far as how useful that debate has been, I think we wait to see. There is a real opportunity there for us to have more co-ordinated effort between the two organisations. I am sure that my Secretary-General will be extremely positive indeed in his engagement with the Parliamentary Assembly.

  Q1031  Lord Desai: You have already mentioned the Paris Declaration and the five criteria that you are using. How do you assess donor countries, whether they are adhering to these five criteria? Secondly, does this initiative contribute to get donors, people like PEPFAR and so on, more into line with the way you think things ought to be?

  Dr Gillespie: Perhaps I will begin and pass to Benedicte for more detail. How do we assess? We run surveys every couple of years—the last survey was in 2006—of the impact of the Paris Declaration. The report, which is in two volumes and quite lengthy, was published last year. In very short terms, there is some progress but much less than we would hope to see.

  Q1032  Lord Desai: Do you construct an index of effectiveness from the five indicators? You have got five indicators and you construct an overall index, do you?

  Dr Gillespie: There are five factors and a number of indicators. Although the factors and the indicators are cross-sectoral, we also look at the number of sectors, so-called tracer sectors, and one of the tracer sectors that we are now looking at is the health sector. That will be one that is focused on particularly at the third High Level Forum in Accra in September. We have data from over 100 donors and around 60 recipient countries. Essentially we do many country reviews of each of the recipient countries, looking at the five factors and the 12 indicators, and publish data which looks across and between both donor countries and organisations and the recipient countries. As I say, in terms of the message from the last survey, a lot more needs to be done. Benedicte can perhaps pick up on some of the key messages and I can turn to the right page in my brief while she speaks. One of the focuses of the Accra High Level Forum will be about implementation of the Paris Declaration. In principle, it provides a basis for much closer integration and alignment of activities, but so far we would say on progress in some areas in all the 60 recipient countries there is progress across the donor community but a lot more needs to be done.

  Dr Callan: One of the things that is different about the Paris Declaration is that it is endorsed by a much larger group of countries, there was broad consultation on agreeing what its goals ought to be and it set targets for 2010. There are three rounds of surveys, one that was done in 2006, one that is being done right now, 2008, for which they are beginning to get preliminary data, and there is one that will be done in 2011 to see whether or not the targets were met. As Iain said, unfortunately the results so far for 2008 show very limited progress towards some of the indicators about alignment of aid. One thing to note is that the survey does not track progress in any one particular sector, so there is not data that is particular to the health sector, which is something that I am sure this group in particular would be interested in seeing. What is important to add to this is that the DAC participates in discussions with the multilateral donors, which is the World Bank but also the philanthropists, in discussing how one is going to monitor progress towards its various goals, including its health outcome goals. There is an ongoing discussion. I know last year they met two or three times to discuss using health as a tracer sector and what indicators they would be looking towards developing and how they would align their own policies. There is an attempt to try to bring in other groups.

  Q1033  Lord Desai: They have accepted your indicator methodology, have they? Are they happy with the methodology?

  Dr Callan: I am sorry, I would not be able to speak to that level of detail. I understand that they are looking towards developing a common methodology, but I could not say whether they have accepted or have not when there are still discussions.

  Q1034  Chairman: Before I move on to intellectual property rights and innovation, can I just ask you this in relation to the answers you have given so far—and it touches on other views we have heard over the preceding months? A picture is coming out, of a network of organisations, NGOs and intergovernmental organisations and so on, and initially we were perhaps thinking it is very crowded and there are too many organisations. But the picture that is emerging is a need to get a clearer view of how they inter-relate with each other, how the networks evolve and where the WHO sits in relation to all of that. There is an element of is the WHO the conductor of an orchestra trying to pull out which bits should be playing with each other and which bits should not. Does that sound sensible to you? I have been influenced in my thinking to some extent by Professor Fidler's evidence to us the other week, which emphasised the networks analogy.

  Dr Gillespie: It is an excellent analogy, it is one that we have used ourselves and tried to follow-up on after Noordwijk. The challenge is the network exists but, if you like, the route through the maze of interactions in the network is poorly articulated and poorly understood, not least by those actors who actually form the network. As to whether there is one conductor or whether there are a number of bandleaders trying to follow a particular score, that is a question that remains open. Certainly the functionality of that network and the efficiency of that network, for us, is the focus of the kind of thinking we in the OECD have been trying to do, not just in this area but in others too.

  Q1035  Chairman: It is very hard to decide whether or not the networks are working to best effect and maximising the use of the finances that are given to them, whether by the UK Government or others, unless you have someone or some organisation taking a bit of an overall view. I suppose one tends to jump to the conclusion that that ought to be the WHO. Is that right or not?

  Dr Gillespie: There are a couple of issues here if we can just slightly unbundle them. The first is the way that the networks align with themselves, so the bottom-up networking, the bottom-up system. There is a lot more that could be done there and there is a great demand from the individual actors, whether they be PDPs or whatever, to develop a better system. That need not necessarily be a top-down issue imposed on them. What we need is space for them to come together to develop these kinds of networks. The second point is one of assessments of what works and what does not work. It is certainly very clear to us in all of those that we have interacted with that we need to be looking at a mix of different interventions to deliver products for Disease X in Country Y. What that mix best is in each circumstance is something which has received scant, if any, attention so far. Which of the interventions actually make and give best value for money also, I am sorry to say, has received scant, if any, attention so far. In mitigation, this is partly because so much of this is so very new. As to whether WHO should be the orchestrator of this, if there were to be one orchestrator it would have to be WHO, but I am not sure whether the one conductor, one orchestrator model is the right one or not. I am not saying it is not, I simply do not know.

  Q1036  Chairman: Do you want to add to that?

  Dr Callan: I like that analogy very much and it is a hugely complex and very difficult field. We are struggling with the question of where the gaps are in the network, where do they fail and what do they fail to do. There are these multiple communities of practice. There is an incredible—and in large part this is thanks to the Bill and Melinda Gates Foundation—renaissance of ideas and groups that are trying to fill in various different gaps. Some of it is gaps in funding, some of it is gaps in information flows. The issue that we are struggling with is that, from a top-down policy level, we can identify certain things, but what really needs to happen is for the researchers, the participants in public-private partnerships, the doctors, to identify for themselves where it is that the network is failing to make an easy flow from the laboratory to the patient's bedside of the types of products that are necessary to reach some of the health outcomes that everybody is hoping to achieve. It is that identification of the gaps that is necessary. On top of which, in certain cases we are jumping quickly to conclusions about what is needed, what are some of the solutions, and for the most part I do not think we know what the solutions are.

  Dr Gillespie: May I just add one thing. We have a group of new tools coming out now, policy tools if you like, that we think from what we can see so far could ease some of these networking problems. The kinds of tools I am speaking about are means to share intellectual property rights around patent pools or patent clearing houses, means to ease access to ideas, to molecules that are partly developed through what we are beginning to see termed as knowledge markets and, also, much more open innovation systems where innovators, even some of the very, very large companies still following a blockbuster model, are looking much more at going out and exchanging ideas and seeing that there is value in knowledge transfer across networks which is above and beyond the proprietary value of the knowledge that they hold. An application of these kinds of systems into the global network that we see here in the global health field could help reduce some of these transaction costs and improve their knowledge flows. We think this because this is what the actors who are trying to achieve knowledge say they are looking to have developed.

  Chairman: Thank you very much. That moves on quite neatly to intellectual property rights and innovation with Lord Avebury.

  Q1037  Lord Avebury: It certainly does lead in to what I was going to ask, which is about the protection and use of intellectual property rights, which you say is necessary but not sufficient for stimulating innovation for neglected and emerging infectious diseases. In your paper you discuss the complementary reward systems which have an important role in incentivising R&D for these diseases, but then you go on to say that further robust analyses are necessary to decide how these mechanisms can best contribute. You have just been talking about one or two of them. Is this a matter on which you are waiting for advice from the World Health Assembly? You said in answer to a question a few minutes ago that the issue of innovation was under discussion there. Have they got these complementary reward systems on the agenda? Do you expect to receive further advice on the subject after that meeting has been concluded?

  Dr Gillespie: Perhaps I could begin by addressing your specific point about WHO and the World Health Assembly and then ask Benedicte to say something more about the specifics of some of the measures we are talking about. What we have seen so far, as an interested party in the process leading up to the World Health Assembly, is a draft strategy which is up for debate now. That draft strategy, if it is adopted, will give us, if you like, the architecture of what the WHO sees as being their priorities for the foreseeable period, at least until the next World Health Assembly a year hence. What we are waiting for is to see which areas of focus WHO will advance on, which areas of focus WHO will look to other organisations to work upon, ourselves included perhaps, and what they will not regard as a priority for them but might be a priority for us in our own work. Essentially, we are looking for complementarity with what comes out of the World Health Assembly. So far, in terms of what we have seen the proposed strategy—and it will doubtless change over the course of this week—has some focus on some of the alternative systems, particularly on so-called prizes for delivery of new molecules. So far it has had a small amount of attention paid to looking at these collaborative systems for interchange of intellectual property rights. That latter area of work, the so-called collaborative mechanisms, pools, clearing houses, et cetera, is an area of work where the OECD already has a substantial head of steam looking at these mechanisms in innovation generally, and global health could be one of them. As to the variety of specific "push" and "pull" mechanisms, the complementary systems, perhaps Benedicte could say a little bit about that.

  Dr Callan: Your question is an interesting one in that it asks, firstly, what are these different mechanisms and whether we are waiting for a signal from the WHO as to whether we are going to do work on them. I would first say that the number of mechanisms that have been proposed to try to accelerate the development and delivery of new vaccines or therapies for diseases of the developing world are not dissimilar from mechanisms being used to develop drugs more generally or that are used to try to reach other public policy goals in other technology areas. The way that these are usually distinguished is there is a category of mechanisms that are "push" mechanisms, which are essentially feeding the innovation pipeline providing subsidies to R&D early on, or pull mechanisms that guarantee a market, guarantee that there is an endpoint.

  Q1038  Lord Avebury: Like the Advance Market Commitment?

  Dr Callan: Exactly, like the Advance Market Commitment, like the prizes, but also things like patent extensions or patent buy-outs which essentially guarantee that there will be a larger financial prize at the end if the innovator decides to invest a certain amount of its R&D into developing new products. These "push" mechanisms, whether it is funding for PDPs, whether it is increased funding for infectious diseases, as the US announced in February of this year, or whether it is pharmaceutical companies that are saying, "We are going to invest more in these particular areas", they are things that the OECD has studied. We have looked at tax credits and what their impact is on firm behaviour. We have looked at subsidies and what their impact is on firm behaviour, whether they are substitutes or complements. These are not things that we are not going to work on, we are working on them in a number of different areas. The question is, do we look particularly at what their impact is going to be on the behaviour of firms who would be willing to invest in infectious diseases. I think that we should be. There is an awful lot of interest in what incentivises firms' behaviour and the OECD is in a good position because it has a good rapport with the industrial sector as a whole and is in constant dialogue with them about how policies actually impact their behaviour. We did some background work on "pull" mechanisms, such as the Advance Market Commitments and IFF. We have looked at what these mechanisms are, what their strengths and weaknesses are, but we have not got to the point that goes beyond what Lord Howarth was saying, which is analysis. We have not got to the point where we have had a discussion amongst countries or communities of users about what kind of policy recommendations or guidelines the OECD might want to put forward. That is the thing that the OECD may be waiting for. We are going to continue working on policy incentives for R&D and what works and what does not work in a variety of different fields. We will certainly continue working on the issues that Iain has talked about, which is all the issues about how you create a smoother knowledge flow of intellectual property, but the question of whether we particularly look at how this is going to change behaviour in one very particular field is something our countries have not come to any decision on.

  Q1039  Lord Avebury: Can I ask, do you think of any particular lessons to be learned from the one really successful initiative, which is Pneumo-ADIP, in the case of the Advance Market Commitment? Is that capable of generalisation or is it a one-off that applies simply to pneumococcal disease? What similar models can you point to that are developed at a theoretical stage which remain to be launched in the case of specific products?

   Dr Gillespie: It is a good question and I wish I had a good answer to it. Unfortunately, we do not, we simply do not know.


 
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