Microsoft word - paper

Global Public-Private Partnerships for Pharmaceuticals:
Operational and Normative Features, Challenges, and Prospects1,2
Sherri A. Brown3
Abstract
Global public-private partnerships (GPPPs) in health have been created, purportedly, as a response to both market and government failure to provide health care goods and services, particularly in developing countries. They have been created to address issues of product development (vaccines or pharmaceuticals), improve access to healthcare products, assist with global coordination mechanisms, strengthen health care services, provide public advocacy and education, and for regulatory and quality assurance purposes. This paper provides an overview of the emerging features of global public-private partnerships in health and argues that GPPPs have real and potential normative and operational implications for national and global health governance. The paper examines two global public-private partnerships in HIV/AIDS-related pharmaceuticals provision: the Accelerated Access Initiative and the Diflucan Partnership Program. It concludes by considering the prospects and challenges of GPPPs as a mechanism of global health governance in advancing health as a global public good. 1. Introduction

Globalizing forces, including increasing interconnectivity in trade, finance, technology, communications, and population mobility have created impacts and challenges for public health that transcend national boundaries. Neither communicable nor non-communicable diseases (tobacco, food and nutrition related conditions, etc) can be contained or addressed solely within individual states. Furthermore, poverty-related diseases (HIV/AIDS, tuberculosis, malaria, etc), have reached epidemic proportions, and have cross-cutting and complex economic, social, and political determinants and impacts. There is a growing awareness that “institutions matter” in devising responses to complex global health issues (Dodgson, Lee & Drager, 2002; Kickbusch, 1997). One of these, enthusiastically recommended as a model for overcoming existing institutional deficiencies, is the phenomenon of global public-private partnerships in health (GPPPs) (Reinecke and Deng, 2000). A GPPP is a collaborative relationship formed between at least three parties: 1) a corporation or industry association, 2) intergovernmental organizations, and 3) national authorities (Buse & Walt, 2001). Global public-private partnerships are created to develop new products (i.e. drugs and vaccines), improve access to products, assist with global coordination mechanisms, strengthen health care services, provide public advocacy and education, and for regulatory and quality assurance purposes (Nishtar, 2004). GPPPs are seen as a response to both market and government failure to provide health care goods and services, particularly in developing countries. Operating under the premise of ‘mutual benefit’, these partnerships are seen to provide needed resources and expertise in exchange for certain tax, marketing, regulatory, and other benefits. Despite the enthusiasm surrounding GPPPs in health in the UN system, at this stage, no global norms or frameworks have been established to help guide the development, implementation, and regulation of GPPPs. Often; in fact, they operate in 1 This paper is part of my dissertation research which is supported by a Social Sciences and Humanities Research Council (SSHRC) Canada Graduate Scholarship (Doctoral). I also gratefully acknowledge the support of the Department of Political Science and Dr. Daniel Cohn. 2 S.A. Brown 2006. Do not cite or reproduce without the permission of the author. 3 Department of Political Science, Simon Fraser University. Email: [email protected] a highly unregulated and/or ad hoc fashion. The ‘blind faith’ accompanying the rising popularity of GPPPs has obscured the development of such frameworks, and there is a need for critical literature and evaluations of GPPPs, both for their normative and operational issues and impacts, as well as for how GPPPs may, as a mechanism of global health governance, impact global health outcomes and cooperation. This paper provides an overview of the emerging architecture in global health governance and situates GPPPs within this architecture. The paper discusses the features and models of global public-private partnerships in health and discusses their real and potential normative and operational implications for national and global health governance. The paper examines two public-private partnerships for pharmaceuticals provision: the Accelerated Access Initiative (AAI) and the Diflucan partnership. The AAI is an initiative hosted by the Joint United Nations Programme for HIV/AIDS (UNAIDS) to facilitate differential pricing negotiations on anti-retroviral therapies for the treatment of HIV/AIDS. The second partnership, the Diflucan Partnership Program, is a partnership between Pfizer and developing states which provides drug treatments for HIV/AIDS-related opportunistic infections. After analyzing the issues and implications associated with GPPPs and the specific cases, this paper considers the prospects and challenges of GPPPs in advancing health as a global public good. An analysis of GPPPs within the framework of the global public goods (GPG) concept provides insight into how these evolving mechanisms of global health governance contribute to global health outcomes and cooperation. Global public-private partnerships in health have real and potential normative and practical implications for national and global health governance, and in their current state, yield little potential for advancing health as a global public good. 2. A Changing Global Order in Health and Health Governance
Health governance has traditionally been the domain of national and sub-national governments. Governments organize and regulate their health systems, and where necessary, coordinate with international organizations, such as the World Health Organization for the purposes of monitoring and controlling health and disease within their boundaries. International health governance (IHG), via organizations like the World Health Organization, has a long history of monitoring and responding to disease outbreaks, setting standards for health reporting, and developing a knowledge base for country information and technical expertise on global health issues. The underlying premise for national and international health governance is that states possess responsibility for health. Globalization, however, has ushered in new challenges for health and is the driving force behind emerging forms of global health governance. Zacher (1999) argues that globalization is reducing the capacity of the state to provide for the health of their domestic populations. Increasing transborder flows of people, information, products (i.e. tobacco, alcohol), externalities (i.e. pollution), create increases in health risks for domestic populations, and thus new challenges for national health governance. It has also been argued that globalization is sustaining or exacerbating economic inequalities and poverty in and among states (Dodgson, Lee, & Drager, 2002), and is thus driving health and disease epidemics such as HIV/AIDS, malaria, tuberculosis, and so forth. For example, there are now approximately 39.4 million people in the world currently living with HIV/AIDS, of which 95% live in the developing world and 64% in sub-Saharan Africa (UNAIDS/WHO, 2004). HIV/AIDS claimed 3.1 million lives in 2004, however, in absolute numbers and as a percentage of the total population, the burden of disease has massively and disproportionately fallen to sub-Saharan Africa (UNAIDS/WHO, 2004). The Joint United Nations Programme (UNAIDS/WHO, 2004) reports that the pandemic has yet to stabilize, although there have been reductions in incidence and prevalence in some countries and regions of the world. However, there is no country or region in the world that has not been affected by the pandemic. Furthermore, the globalization of disease is not restricted to HIV/AIDS. Disease epidemics in malaria, tuberculosis, and other infectious diseases are exerting enormous pressures on health infrastructures and exacting massive morbidity and mortality tolls. Emerging infectious diseases such as SARS and avian flu have the potential to reach epidemic proportions. Non-communicable diseases including cardiovascular diseases and cancers are also increasing at alarming proportions in developed and developing countries. Developing countries are expected to experience a double-burden: increasing communicable and non-communicable diseases. Ultimately, Lee (1999) argues that globalization is contributing to greater inequities in health, where poor and marginalized countries and populations share an expanding proportion of the global disease and poor health burden. These trends have exposed the limitations of domestic health governance in a globalizing world. Governments are increasingly looking toward new forms of cooperation such as treaties4, global public policy networks, public-private partnerships (PPPs), and other arrangements. Health care promotion and provision is increasingly characterized by a shift from government to governance modalities. Dodgson, Lee, & Drager (2002) distinguish government from governance and describe governance as the “actions and means adopted by a society to promote collective action and deliver collective solutions in pursuit of common goals” (6). Governance can be ‘disentangled’ from government (Reinicke, 1997; Rosenau & Czempiel, 1992) to describe formal or informal activities and mechanisms in the pursuit of common social goals and objectives. There has been a growth in the number and influence of non-state actors in health governance (Dodgson, Lee, & Drager, 2002). Civil society groups, social movements, private corporations, consultancies, think tanks and research institutes, and religious movements are participating in health governance through their roles in advocacy, policy formation, policy implementation, service and product provision, and research and development. Moreover, many of the traditional health governance functions of the state are being devolved to non-state actors (for example, transferring ownership or responsibility for health services to the private sector or non-governmental organizations), or supplemented by non-state actors (new combinations of state and non-state actors in health governance).Dodgson, Lee, & Drager (2002) refer to the latter as the “hybridization of governance” (6), which includes the “growing partnerships of public institutions with the private sector” (McBride, 2004,5). This paper conceptualizes global public-private partnerships as the hybridization of governance (Dodgson, Lee & Drager, 2002) Hybridization and Mixed Actor Governance
The delegation of governance functions to private actors is not an innovative practice. At the domestic level, states have been delegating governance functions to private actors via privatization, de-regulation, and transformations in the public service (i.e. the use of private consultants). Domestic health governance has typically consisted of mixed actors, including public actors (states, bureaucracies, etc) and private actors (community and faith-based organizations, private corporations, health practitioners, associations, etc). Partnerships between 4 For example, the Framework Convention on Tobacco Control specifies principles for global tobacco supply and demand reduction. The Framework entered into force in February 2005 and currently consists of 126 parties (as of May 16, 2006). the public and private sector (particularly corporations) at the domestic level have become commonplace, particularly in western developed countries. Although these governance combinations are not new at the domestic level, they are relatively new at the international level (Börzel & Risse, 2005; Witte & Reinicke, 2005). These new partnerships are referred to as ‘global’ (rather than ‘international’) public-private partnerships because they involve non-state actors5 which are generally of a transnational character. These partnerships delegate specific tasks and roles to private actors, particularly transnational corporations and private foundations. Börzel & Risse (2005) identify three main purposes of global public private partnerships: 1) rule and standard setting, 2) rule implementation, and 3) service provision. Global public-private partnerships are an example of a relatively new form of health governance that involves a combination of state and non-state actors. Under globalization, the traditional state-centric system of health governance is transforming, both in terms of the complexity of the health challenges that states encounter, and the responses, which are increasingly global and mixed actor in nature. Global public-private partnerships are gaining considerable popularity as an institutional mechanism of global health governance to address global health issues. However, there are a multitude of challenges associated with these new forms of governance, which are explored in the subsequent sections of this paper. 3. Global Public-Private Partnerships in Health: An Overview

Global public-private partnerships are voluntary and collaborative relationships (Dodgson, Lee, & Drager, 2002; Nelson, 2002) that bring together state and non-state actors to undertake specific functions in health governance. Nelson (2002) suggests that partners agree to “share risks, responsibilities, resources, competencies and benefits” (47). There is considerable confusion, as well as controversy surrounding the definition and parameters of global public-private partnerships. Richter (2004) suggests that the term “partnership” for these configurations is ‘value-laden’ (47) because it assumes that the roles, responsibilities, and benefits of partnership are equal. Hence, the use of the term ‘partnership’ carries a positive or neutral connotation, which potentially obscures the negative or problematic aspects of the arrangements. Martens (2003) criticizes the term, noting that it elevates and legitimizes the status of private actors, while concomitantly downgrading the status of the public sector in the area or issues of health governance are addressed by the partnership. At a meeting of public-private partnerships participants involved in drug delivery, Buse (2001) reflected on some of the confusion surrounding the critical attributes of partnerships. Meeting participants failed to arrive at a consensus on whether partnerships needed to be based on shared goals, shared decision-making, a division of labour, and/or mutual contributions of human, physical, and capital resources (Buse, 2001:7). A more detailed discussion about the appropriateness of the term ‘partnership’ to describe these configurations is beyond the scope of this paper, however, it is important to note that the term, in its most positive or even neutral connotations, inevitably belies the need for more thorough and critical evaluations of the normative and practical implications of GPPPs for national and global health governance. The proliferation of global public-private partnerships in health reached an apex in 2000, with the addition of 17 new partnerships. Fifty of the partnerships were established between the 5 Partnerships for pharmaceuticals provision are primarily composed of private sector (commercial and/or corporate foundation) partners. years 1998 and 2003.6 Most of the 92 existing partnerships in health address infectious diseases.
Out of the 92 GPPPs, 84 address infectious or communicable diseases, with the remaining eight
covering issues such as chemical safety, injection safety and syringes, harmonization of drug
applications, diarrhea, counterfeit and substandard drugs, health systems and policies,
micronutrient or vitamin deficiencies, and technical support. 7 HIV/AIDS is the main disease
addressed by public-private partnerships. Nineteen (19) of the public-private partnerships
identify HIV/AIDS as the health condition addressed by the partnership. Furthermore, 59 of the
92 partnerships are devoted to drug, health products or vaccine development or distribution, and
30 address health systems, services, or policies. There are several different configurations of
global public-private partnerships; however, Evans & Chen (2005) describe two broad
groupings. The first type, partnerships operated by International Agencies, invites participation
of private sector actors. These partnerships are under the administrative and financial control the
United Nations, or World Bank staff and systems (Evans & Chen, 2005). The Roll Back Malaria
Initiative, Stop TB Initiative, and the Accelerated Access Initiative (AAI) are examples of this
type of partnership. The other grouping includes partnerships that are independently structured
non-profit entities with private governance, operations, and financing (Evans & Chen, 2005),
such as the Diflucan Partnership, which will be discussed in a later section of the paper.

Rationale for Partnership

The rationale for global PPPs in health is that they are a response to both market failure (Evans & Chen, 2005) and institutional failure or lethargy (Holm, 2001; Evans & Chen, 2005) to
provide health care goods and services, particularly in developing countries. Other explanations
for the development and growth of GPPPS suggest that neo-liberalism, and its emphasis on the
retrenchment of the public sector in social policy and programs (including health) has shifted
responsibility and engendered opportunity for private sector involvement (Holm, 2001; Evans &
Chen, 2005). Finally, GPPPs are seen as an “unavoidable necessity” in harnessing the necessary
resources to address increasingly complex, inter-related, global health issues (Brundtland, 2002).
The United Nations lists GPPPs on their list of approaches to make UN agencies more efficient
and effective, and increasingly UN agencies are promoting closer ties with the business
community (Richter, 2004).

Benefits to the Private Sector

Partnerships afford numerous benefits to private sector partners, including direct financial returns, whether through tax breaks or payment for services or products (for example, some partnerships between pharmaceutical companies and states negotiate discounted drug pricing instead of donations). Buse & Walt (2000) refer to the fact that many of the contributions made by private sector partners are tax deductible. Partnerships allow the private sector to penetrate a market that may have previously been inaccessible, and promote their image and brand (Buse & Walt, 2000). Partnerships provide enhanced corporate legitimacy and authority with institutions such as the United Nations and other bodies (Buse & Walt, 2000). Indeed, Buse & Walt (2000) argue that the costs associated with many of the private sector contributions are relatively small compared to the benefits arising out these partnerships. For example, Bristol-Myers Squibb’s 6 www.ippph.org/index.cfm?page=/ippph/partnerships/date_established 7 Initiative for Public-Private Partnerships in Health Partnerships Database: www.ippph.org/index.cfm?page=/ippph/partnerships/disease annual contribution of US$20 million represents 0.1% of the companies US$18.3 billion in
annual sales (Buse & Walt, 2000:706).
Benefits to National and Global Health

Partnerships provide resources to national and global health governance in the form of drugs, supplies, services, or funds (Holm, 2001). Partnerships also provide skills, expertise, and
management to health interventions. For example, the African Comprehensive HIV/AIDS
partnership (ACHAP)8, a partnership between the Bill and Melinda Gates Foundation and Merck
Foundation, has provided training to over 500 Government, NGO and other actors in project
development, monitoring, evaluation, proposal development, media training, and computer
skills, as well as training for over 1200 health care workers.9 ACHAP reports that over 12,000
people have been enrolled into the national anti-retroviral treatment program. Partnerships, such
as the Mectizan® Donation program, have largely contributed to the eradication of blinding
onchocerciasis (Buse & Walt, 2000:706).

4. Operational Issues and Challenges of GPPPS: Governing Arrangements, Transparency,
Accountability, Outcome Orientations, and Sustainability

Much of the criticism launched against public-private partnerships pertains to their governing arrangements. There are concerns with GPPPs in terms of real and potential conflict of interest situations, accountability, transparency, decision-making structures and participation, sustainability, and outcome orientations. In terms of membership, there are substantial problems with the selection and representation of partners. Richter (2004) contends that corporate partners are not adequately scrutinized by international agency partners for potential conflicts of interest. Buse’s (2004) study supports Richter’s claim, noting that only four (4) out of the nineteen (19) partnerships in his study undertook formal assessments of the background of their commercial partners. Buse (2004) notes that this oversight is occurring in both international agency and non-profit entity partnerships, and suggests that where guidelines exist in international agencies governing corporate selection, “they are not widely adhered to” (238). Furthermore, as Buse (2004) notes, there is a “gross under representation of southern stakeholders” (240) in the governing arrangements of GPPPs. Out of the 92 global public-private partnerships in health listed in the Initiative for Public Private Partnerships in Health (IPPPH) database, all but four (4) have Secretariats in northern countries (North America and Western Europe).10 Only two (2) of the partnerships have Secretariats in Africa (Kenya and South Africa). Approximately 40% of the partnership secretariats are located in the United States and 35% are located in Switzerland11. What is the nature of ‘partnership’ and the potential for meaningful involvement and representation in the processes of decision-making for developing countries when the loci of decision-making are concentrated in northern countries? Kickbusch (1997) argues that one of the critical processes associated with the globalization of health is that decision-making processes are increasingly inaccessible to the public. GPPPs have the potential for exacerbating the problems of transparency and 8 The ACHAP website is located at: www.achap.org 9 www.ippph.org/index.cfm?page=/ippph/partnerships/name&thechoice=show&id=49&typobj=0 10 Access to the Initiative for Public-Private Partnerships in Health (IPPPH) database is available to the public, but requires registration with the Secretariat. Permission to use the database was obtained on November 2, 2005. Database: http://www.ippph.org/index.cfm?page=/ippph/partnerships 11 Data obtained from the www.ippph.org and calculated by the author. representation in decision-making. While partnerships make basic information (profile, programmes, partners, contacts, public relations material) 12 available on their websites, few partnerships post annual budgets or program evaluation/impact documentation. Where publications are posted to the website, they largely resemble public relations material detailing the ‘successes’ of the programs. In a study by Buse (2004) he found that none of the partnerships with independent legal status make available the minutes of their deliberations (237). Buse (2004) also notes that while auditing practices are common in GPPPs, they are not practiced by all partnerships. Buse (2004) concludes that regardless of whether the partnership is a publicly or privately hosted partnership, very little information is made publicly available on the partnerships’ governing arrangements. There is considerable discussion on the issue of accountability of GPPPs in the literature (Nishtar, 2004; Buse, 2004; Evans & Chen, 2005; Buse & Walt, 2000). Questions are raised as to whom the partners are actually accountable to, as well as the availability and employment of reporting mechanisms (Buse, 2004). Are the funders accountable to the partner countries or international agencies or to their own stakeholders? What are the measures of accountability? Are they purely fiscal or are there other evaluations of performance? How and to whom are these reported? Who are the partnering countries/agencies accountable to? To their citizens/constituent members and/or the funders? How are these reported? What are the consequences of poor performance by partners? By what criteria are the partners judged on measures of accountability? These and other questions have yet to be resolved and will continue to call into question the legitimacy and feasibility of GPPPs as a mechanism of global health governance. There are also challenges and controversies with the outcome orientations of GPPPS. Partnerships in general report effectiveness in terms of value-added contributions (see Holm, 2001). Partnerships often report on the number of drug units distributed, the number of personnel trained, the total funds distributed, and other quantitative impacts.13 For example, the AAI and Diflucan Partnership make this type of information available, but offer very little publicly available information on partnership governing arrangements and other operational aspects. There is little information on whether the partnerships actually contribute to improvements in the quality and efficiency of drug donations, health services, research, public information and advocacy, and product development. There is very little empirical data or even anecdotal information on how partnerships interface with national health governance institutions and structures. Very little consideration is afforded to the potential problems or unintended side-effects of partnerships; partnerships tend to emphasize their value-added and functional contributions. Further complicating these issues, Holm (2001) notes that there is very little baseline data upon which to conduct research on the effectiveness of partnerships in their specific contributions to health or health outcomes. There are serious concerns surrounding the sustainability of the partnerships. Some of the partnerships do not have stated timelines, some have guaranteed drug donation until there is evidence of disease eradication (i.e. Merck & Co. Mectizan® donation) , while others have between three and six year life spans, after which the partnership is either terminated, or extended by agreement of the parties involved. Some partnerships, such as Global Alliance for Vaccines and Immunizations (GAVI) have been criticized for not only their organizational 12 See www.achap.org (African Comprehensive HIV/AIDS Partnership); www.securethefuture.com (Secure the Future); www.diflucanpartnership.com Diflucan Partnership, www.lillymdr-tb.com/ Eli Lilly Multi-Drug Resistant Tuberculosis Partnership; www.iavi.org International AIDS Vaccine Initiative, for a small cross-section of partnership websites. Note that not all partnerships have websites. 13 See www.ippph.org health partnerships database for information on partnership impacts (including publications on impact). sustainability, but for their financial sustainability as well. Nishtar (2004) looks at GAVI as an
example of a GPPP that emphasizes high technology vaccines, relies heavily on the private
sector, and “runs the risk of compounding health inequities in developing countries” (5). Yamey
(2001) makes similar conclusions in his study of GAVI, revealing that the vaccines were being
sent to countries that already had some basic immunization coverage, while the poorest countries
that lacked even basic immunization coverage (tetanus, polio, diphtheria) were not covered under
GAVI. Furthermore, there is a question of whether drug donations are sustainable models for the
provision of essential medicines (Gardiner, 2003). These partnerships, despite providing needed
resources for the treatment of diseases and health conditions, are nonetheless a charity model of
health, rather than a model of global collective action and responsibility for health. This model
necessitates dependency on the donor, who may or may not continue their programs upon
expiration. Policy levers or instruments compelling the donors to continue their programs are
non-existent, and short of moralsuasion and tax-breaks, leave the recipient countries and
agencies largely at the mercy of the donors. GPPPs have responded (see Holm, 2001) to
criticisms of sustainability, noting that many public sector organizations often do not make
program commitments for longer than five years. While public sector organizations could
potentially be charged with many of the same governance deficiencies and controversies as the
partnerships, there is at minimum, accountability expectations and mechanisms in public sector
organizations that do not necessarily exist in the partnerships, particularly those that are
independent non-profit entities.

Normative and Operational Interfaces between National Health Governance and Global
Public-Private Partnerships

Interfaces between institutions and structures of national health governance and the partnerships are rarely revealed by the partnerships themselves, and are only beginning to be considered in academic (Nishtar, 2004) and policy (See Holm, 2001; Caines & Lush, 2004) literature. Moreover, very few studies exist that investigate the obstacles and unintended side-effects of implementation, integration, and management of partnerships with existing health governance structures and institutions. Caines & Lush (2004) examine a cross-section of pharmaceutical partnerships in low and middle income countries, and identify several issues with how these partnerships impact health governance. For example, their report reveals evidence that partnerships faced a low level of trust between governments and the pharmaceutical industry, and affected local competition of pharmaceutical sales (Caines & Lush, 2004). Perhaps partly due to the emphasis on the ‘value-added’ aspects of partnerships, very little consideration is given to the actual costs of involvement. Partnerships have the potential to overwhelm the capacity of the national health system (Holm, 2001; Caines & Lush, 2004). Sturchio & Cotarella (undated) note in their assessment of the Merck’s Ivermectin donation program that poor community health infrastructure in many of the countries most affected by river blindness impeded drug distribution. Thus, partnerships, particularly those in developing countries, are likely to confront inadequate health infrastructure, and have the potential to overwhelm already overextended health personnel and infrastructure. Moreover, because very few partnerships14 actually address more than one aspect of health (product development, access to products, health systems and services, research, public information and advocacy, and coordination), the 14 Four of the 92 partnerships listed with the IPPPH address more than one aspect of health. Figure obtained from the Initiative for Public-Private Partnerships in Health Database partnerships are, for the most part, vertical programs that require integration into existing health infrastructures and strategies, and could possibly contribute to the fragmentation of health systems (Buse, 2004; Nishtar). Nishtar (2004) considers the potential normative implications of GPPPS, and argues that they have the potential to alter public priorities, redirect national policies, and shift public
responsibility for health to the private sector. GPPPs have the potential to contribute to the
further commercialization and privatization of health governance by weakening the role of the
public sector in providing essential health services and treatments and by transferring this
responsibility to private sectors partners. Given what we already know about some of the
negative impacts of economic globalization and global restructuring on national health systems
(See Bienan & Shelton, 2001; Birdsall & Lawrence, 1999; Coburn, 2000; Haddad & Mohindra,
2001), are GPPPs contributing to or mitigating against the hollowing out of the state’s capacity
and autonomy to deliver health services? This is a question for future research, but one that
deserves closer investigation. Are GPPPs simply new forms of developing country dependency
on developed countries? Given that very few of the partnerships involve real transfers in
knowledge, or building of new infrastructure, and that the intellectual property generated by
these partnerships (i.e. in vaccine development) will be largely retained by researchers in the
north, how do these partnerships, beyond the value-added component, contribute to the building
of equitable, sustainable health systems in developing countries? The literature on public-private
partnerships has yet to answer these questions.

Normative and Operational Interfaces between Global Health Governance and Global Public-
Private Partnerships

Global public-private partnerships in health have implications for global health governance vis-à-vis their enhanced role in global public policy making. Given their growing popularity as a mechanism of health governance, there are reasonable concerns over enhanced corporate influence in setting the global health agenda (Richter, 2004). Buse & Walt (2000) argue that partnerships have increased corporate influence in policy making at global and national levels. Furthermore, there are implications for global health governance institutions in embracing the use of GPPPs. Richter (2004) argues that GPPPs pose a risk to the “integrity, independence, and reputation” of the United Nations (48). Buse & Walt (2000) question the appropriateness of using public money (in the partnership arrangements) to support corporate legitimacy. These partnerships open up considerable space for private sector influence in global health decision-making, and Buse & Walt (2000) argue that this weakens the ‘universality’ of multilateral institutions, and could potentially undermine traditional support for the UN. The latter part of their argument is rather unconvincing, however, given that governments around the world are increasingly employing public-private partnerships as a mechanism of service delivery. Despite the issues and implications with public-private partnerships, governments and multilateral institutions at this point seem to be readily embracing them. Dodgson, Lee & Drager (2002) argue that there is a need for “consensus about the underlying moral and ethical principles that guide global health cooperation” (21). Currently, the de facto consensus in the UN system supports the use and proliferation of global public-private partnerships in health. At this time, there is very little empirical data available with which to test and assess these claims. This paper forms part of a larger research program that will examine the normative and operational issues and challenges of partnerships through an investigation of two selected public-private partnerships in pharmaceuticals provision: the Accelerated Access Initiative and the Diflucan Partnership. The next section of the paper overviews these two partnerships, including their real and potential normative and operational implications for national and global health governance. 5. Public-Private Partnerships in Health and Access to Pharmaceuticals
It is now widely acknowledged that over one-third of the world’s population lacks access to essential medicines, including HIV/AIDS-related medicines (Sterckx, 2004). Of this group, over 50% live in the least developed countries in Africa and Asia (Sterckx, 2004). Drug access, particularly for those living in countries with endemic infectious diseases, including HIV/AIDS, malaria, and tuberculosis, has become a matter of life and death. Fifteen years following the first case of AIDS15, new hope emerged with the advent of highly active antiretroviral therapies. These ARV therapies were successful in providing life-sustaining support for people living with HIV/AIDS. While these therapies have been available since 1996, high prices of these drugs have made them out of reach for the majority of people living with HIV/AIDS. In the western developed world, ARV treatments can cost between $10,000-15,000 per person per year (Joseph, 2003). In a 1993 Report, “Investing in Health," the World Bank reported that per capita spending on health was as low as US$8 in the least developed countries. Clearly, these and other developing countries, as well as countries with economies in transition, were ill-equipped to offer these drugs as part of their health care delivery. Moreover, the high cost of these drugs made them largely prohibitive for the majority of individuals residing in these countries. Currently, 440,000 people in low and middle-income countries have access to anti-retroviral treatment (ARV), however, this means that 9 out of 10 people who need ARV currently do not have access (UNAIDS/WHO, 2004). If access to ARV remains at this level, approximately five to six million people are projected to die within the next two years (UNAIDS/WHO, 2004). Pharmaceutical companies initially advanced an economic/property narrative on the issue of drug access. They argued that there was no relationship between the drug prices and access; rather, they claimed, that social, political, and infrastructural barriers impeded the broad rollout of complicated HIV/AIDS medications (Gellman, 2000; Joseph, 2003). Eventually, pharmaceutical companies conceded that prices charged for their drugs in developing countries made them largely prohibitive. However, they also argued that patent protection was necessary to stimulate drug research and development. International and domestic civil society organizations, including the Treatment Action Campaign (TAC) in South Africa16, Oxfam17, and Médecins Sans Frontieres18 had conceptualized the issue differently and drew attention to the issue of patent protection, patent abuses, and the lack of generic competition in constraining access to HIV/AIDS-related pharmaceuticals. Furthermore, groups, such as the Harvard Consensus group refuted claims that it was not possible to administer widespread HIV treatment in poor countries.19 The claim by pharmaceutical companies that patent protection is necessary to 15 The first recorded case of AIDS was in 1981. 16 See http://www.tac.org.za 17 See http://www.oxfam.org 18 See http://www.msf.org 19 Consensus Statement on Antiretroviral Treatment for AIDS in Poor Countries By Individual Members of the Faculty of Harvard University, 2001.See: www.hsph.harvard.edu/bioethics/pdf/consensus_aids_therapy.pdf stimulate research and development has also been challenged.20 Ultimately, however, the problem became defined as one of affordability for developing countries. The natural solution was therefore to provide deep price discounts or donations to developing countries to enhance access to these drugs. The Accelerated Access Initiative and Diflucan Partnerships emerged in these contexts to provide deeply discounted or donated HIV/AIDS-related pharmaceuticals. The Accelerated Access Initiative
The Accelerated Access Initiative and the Diflucan Partnership were intended to ‘problem-solve’ the ‘accessibility’ issue of HIV/AIDS related pharmaceutical products. AAI was intended to increase access to anti-retroviral therapies which provide life-sustaining support to people living with HIV/AIDS. The Diflucan Partnership provides fluconazole (brand name ‘Diflucan’), an anti-fungal drug for the treatment of HIV/AIDS-related opportunistic infections. The Accelerated Access Initiative was announced in May 2000 and consists of a partnership between five UN organizations21 and six pharmaceutical companies22. The partnership, according to the Initiative for Public-Private Partnerships23, was intended to address issues of drug access and affordability in the “hardest hit regions of the world.”24 Currently, 17 countries are participating in the AAI (See Table 1.0). The AAI does not have separate legal status, and is coordinated by the Secretariat of the Joint United Nations Programme on HIV/AIDS (UNAIDS) in Geneva, Switzerland. The AAI works with governments, international organizations and the private sector to negotiate differential drug prices. Thus, all funding for HIV/AIDS pharmaceuticals comes from the countries themselves. Although the international public sector partners are involved in negotiating drug discounts, these negotiations occur primarily on a bilateral basis. Differential pricing negotiations are conducted with individual pharmaceutical companies on a country-by-country basis, although there is some indication that the Initiative may be working towards a regional collaboration approach. AAI indicates that these negotiations are available to countries that can “provide proof they have the health services to handle the complicated HIV/AIDS medicines.”25 This is an important equity consideration of the AAI. Partnerships that select countries on the basis of existing health infrastructure inherently exclude countries that may desperately need discounted drugs, but are unable to access them because of ‘inadequate’ health systems and thus could exacerbate global health inequities. It is important to 20 For example, Bettcher, Yach & Guindon (2000) argue that the premises of patent protection, (to stimulate innovation and generate money for research and development), fail to recognize that considerable research and development is conducted using government monies, that patents and intellectual property rights are relatively recent phenomena, that innovation and research and development has occurred in the absence of patent protection, and that intellectual property rights are afforded only when a country has achieved a certain level of economic development. 21 World Health Organization, United Nations Children’s Fund, United Nations Population Fund, the World Bank, and the Secretariat of the Joint United Nations Programme for HIV/AIDS UNAIDS 22 Abbott Laboratories, Boehringer Ingelheim, Bristol-Myers Squibb, F. Hoffman-La Roche, GlaxoSmithKline and Merck and Co., Inc 23 The Initiative (IPPPH), defunct as of December 2004, was set up by the Global Forum for Health Research (http://www.globalforumhealth.org/Site/000__Home.php), an independent international foundation promoting global health research. The IPPPH website is www.ippph.org . The website houses a publicly accessible ‘health partnerships’ database which contains information on global public-private partnerships and is updated by the Global Forum on Health Research. 24 www.ippph.org/index.cfm?page=/ippph/partnerships/name&thechoice=show&id=2&typobj=0&id_ chapter= abstract 25 Ibid. note that of the 17 countries participating in the AAI, only 626 are considered ‘high HIV/AIDS burden’ countries by the World Health Organization (WHO, 2005). The WHO lauds the success of the Initiative, claiming that a total of 427,000 people living with HIV/AIDS in developing countries receive ARV treatment provided by AAI companies.27 It is not clear how many of these people were recipients of treatment as a direct result of AAI-facilitated negotiations. However, the Initiative emphasizes the value-added benefits of the partnerships and claims that since its establishment there has been as 23-fold increase in the number of people receiving treatment from AAI companies.28 The Initiative also claims that it has achieved significant price reductions on HIV/AIDS-related pharmaceutical products.29 The AAI, from a functional or problem-solving perspective, has been quite effective. By negotiating lower drug prices, the Initiative has facilitated greater access to HIV/AIDS-related medicines. However, as discussed in section 4.0, there are normative and operational issues and challenges associated with the AAI. In terms of its governing arrangements, Buse (2004) notes that the executive of the AAI is not accountable to the governing body of the partnership (the Secretariat) but to the host organization. Buse (2004) argues that this limits the extent to which the partners can hold the Secretariat accountable for the workings of the partnership. The AAI also does not make available information on the management of its governing bodies or decision-making processes, nor does it publish (on Internet sites) its sources of funding or negotiated drug prices. Thomas (2002) identifies real concerns with bargaining procedures and implications of the AAI and criticizes the AAI as an institution which reinforces and perpetuates structural inequality. Thomas (2002) argues that requiring countries to negotiate with individual pharmaceutical companies compromises their negotiating position. Table 2.0 presents total revenues and net incomes of AAI participating pharmaceutical companies from 2004 and 200530. When contrasting these figures to countries’ GNI and GDP, it can be seen that only 6 of the 17 countries’ GNI from 2004 is equal to or greater than the pharmaceutical company with lowest total revenues in 2004 (Boehringer Ingelheim at $10.3 billion). Furthermore, 7 of the 17 countries are classified as severely indebted by the World Bank, 4 are moderately indebted, and 5 are less indebted (World Bank List of Economies, July 2005). This rather crude comparison nonetheless demonstrates the unequal bargaining positions of developing countries and pharmaceutical companies. Table 1.0: Accelerated Access Initiative Country Participants
AAI Participants
2004 GNI-31
Atlas Method
($US dollars)
GNI Per Capita
($US dollars)
($US Dollars)
26 See Table 1.0. High burden countries are identified by ‘hbc’ in the AAI participants column. 27 See AAI fact sheet for more information: www.who.int/entity/hiv/AAI_fs_4Q2005.pdf 28 Ibid. 29 www.ippph.org/index.cfm?page=/ippph/partnerships/name&thechoice=show&id=2&typobj= 0&id_chapter=impact 30 Pfizer, Inc. is not a participating company in the AAI. Data from Pfizer, Inc is presented in this Table in reference to the Diflucan Partnership. 31 All economic data obtained from the World Bank website on country data: http://web.worldbank.org/WBSITE/EXTERNAL/COUNTRIES/0,,pagePK:180619~theSitePK:136917,00.html Burkina Faso hbc
Burundi- hbc
Cameroon- hbc
Republic of Congo
Democratic Republic of Congo
Cote d’Ivoire- hbc
Rwanda- hbc
Trinidad & Tobago
Uganda- hbc
Table 2.0: Pharmaceutical Companies Total Revenues and Net Incomes from 2004 & 2005
Pharmaceutical Company32
Total Revenues 2005
Net Income 2005
Total Revenues 2004
($US Dollars)33
($US Dollars)
Abbott Laboratories
Boehringer Ingelheim35
Bristol-Myers Squibb
F. Hoffman-La37 Roche
GlaxoSmithKline38
Merck and Co., Inc
Pfizer Inc.
While Buse (2004) notes that the AAI was one of only four partnerships in his study39 to undertake a formal assessment of the commercial partners in the partnership, he also refers to the 32 Financial data from pharmaceutical companies has been obtained from 2005 Annual Reports. All reports are publicly available on company websites: Abbott- www.abbott.com; Boehringer Ingelheim www.boehringer-ingelheim.com; Bristol Myers Squibb- www.bms.com; F. Hoffman-LaRoche- www.roche.com; GlaxoSmithKline- www.gsk.com; Merck and Co., Inc- www.merck.com; Pfizer- www.pfizer.com. 33 All figures in the table have been rounded down to the nearest million. 34 Net income amounts from 2005 and 2004 are reported as ‘after tax’ income. 35 Amounts in Annual Report presented in Euros. Table reflects conversion to US$ based on nominal exchange rate of 1.1841 (rate from December 30, 2005). Conversion tables obtained from Bank of Canada Rates and Statistics: www.bankofcanada.ca/en/rates/exchform.html 36 Net income amounts from 2005 and 2004 are reported as ‘after tax’ income. 37 Amounts in Annual Report presented in Swiss Francs. Table reflects conversion to US$ based on nominal exchange rate of 0.7598 (rate from December 30, 2005). Conversion tables obtained from Bank of Canada Rates and Statistics: www.bankofcanada.ca/en/rates/exchform.html 38 Amounts in Annual Report presented in U.K. pounds. Table reflects conversion to US$ based on nominal exchange rate of 0.7598 (rate from December 30, 2005). Conversion tables obtained from Bank of Canada Rates and Statistics: www.bankofcanada.ca/en/rates/exchform.html 39 Buse’s (2004) study undertook an analysis of the governing arrangements of nineteen global public-private partnerships. limited pool of partner choices given the monopoly positions and patent protection afforded to pharmaceutical companies. At this point, there are several normative and operational challenges, including governing arrangements, transparency, sustainability, accountability, southern representation and bargaining procedures, outcome orientations and equity considerations. Continuing research on the AAI will examine the normative and operational interfaces and impacts of the partnership on national health governance, including health systems, policy and decision-making and local pharmaceutical markets and distribution systems. The Diflucan Partnership
The Diflucan Partnership40 is actually more appropriately conceptualized as a donation programme. It was launched in December 2000 by Pfizer Inc.41 in South Africa and has since expanded to over twenty-nine developing countries. Diflucan, also known as fluconazole, is an antifungal medicine for the treatment of fungal opportunistic infections such as cryptococcal meningitis and esophageal candidiasis. These infections regularly present in people living with HIV/AIDS. Although the partnership does not have dollar or time estimates, Pfizer has estimated the total cost of its partnership commitments to be US$103 million (as of 2004), which represents 0.19% of total revenues for Pfizer in 2004.42 Of what little information is available on the partnership, Pfizer claims that it has distributed 7 million free doses of Diflucan to 1,100 sites in 42 developing countries across Africa, Asia, Latin America and the Caribbean.43 The programme also trains health personnel in the treatment of opportunistic infections and appropriate dosing protocols. Pfizer, Inc. estimates the initial cost of training at US$2 million. Weartheimer, Santella & Lauver (2004) note that the program has since expanded and trained and additional 9,000 health care workers. The Diflucan Partnership makes available this type of ‘value-added’ information on its website, yet like the AAI, offers no information on its negotiating and governing arrangements. Furthermore, there is no empirical data available to assess equity considerations in partnership development (i.e. how are these drugs being made available within the country? and to whom?), or in terms of the impact of partnerships on health governance structures, including policy and decision-making structures, local pharmaceutical markets, and health care systems. Pfizer makes their drugs available only to public sector and NGO partners, and thus there are likely effects on local pharmaceutical markets. Furthermore, there is also the question of the long-term sustainability of drug donation models (Gardiner, 2003). In addition to some of the issues identified with public-private partnerships in section 4.0, an analysis of this partnership reveals how social relations figured significantly into its genesis. In South Africa, where the partnership was first launched, initially high prices of fluconazole constrained widespread access. The Treatment Action Campaign launched a major campaign against the high price of fluconazole on March 13, 200044. Initially, TAC demanded that Pfizer, Inc. reduce its drug prices45, citing significantly lower prices in the public sector in South Africa 40 www.diflucanpartnership.org 41 Pfizer, Inc., is the world’s largest pharmaceutical company (See Table 2.0). 42 Based on data obtained from Pfizer Annual Report 2005 43 www.ippph.org/index.cfm?page=/ippph/partnerships/name&thechoice=show&id=73&typobj=0 44 Obtained from: www.tac.org.za 45 TAC launched a major campaign on March 13,2000 to reduce the price of fluconazole. In written correspondence to the and internationally46. When Pfizer, Inc., failed to meet their requests, the Treatment Action Campaign demanded generic competition of fluconazole47,48. The campaign resulted in mass protests to demand that the Medicines Control Council of South Africa grant a ‘Section 21’ exemption to the generic importation of fluconazole (‘biozole’) from Thailand. Within weeks of the filing, Pfizer announced that it would donate fluconazole to the public sector for people with cryptococcal meningitis and systemic thrush.49 The donation programme would provide drugs only to the public sector, and Pfizer refused to grant a voluntary license for fluconazole production in South Africa. However, when Pfizer, Inc., failed to roll out its donation programme in a timely manner, TAC began importing generic fluconazole for distribution.50 Pfizer eventually responded and accelerated its donation distribution. Because Pfizer’s patent on fluconazole expired in 200451, it has been eager to gain a market threshold in many other developing countries, and continues to expand its donation programme. The Diflucan Partnership is therefore not merely a ‘functional’ or ‘problem-solving’ response to high drug prices. The partnership is, in some senses, an institutional compromise
midwifed by conflict between public and private interests. The South African government has
not, and likely will not, exercise its options under the TRIPs safeguards52. If the South African
government were to exercise its options, this would substantially drive down the prices of the
drugs through generic competition. Until such time as Pfizer withdraws from the partnership, the
South African government and peoples are beholden to Pfizer, dependent upon its potentially
fickle generosity. Pfizer’s private interests in the market are secured and enhanced by the
partnership53; they are insulated from compulsory licensing and parallel importation and generic
competition; the partnership provides much needed favourable publicity, and offers lucrative tax
deductions on their donations in the United States, all at very little cost to their bottom line. The
normative and operational impacts of these partnerships for national and global health
governance require further investigation, although, it can be argued at this point, that there are
important normative and operational issues which necessitate scrutiny, and hence, reform.

6. Concepts of Health and Cooperation in Global Health

Global Public Goods (GPG) Framework for Global Health Cooperation

In traditional economic theory, public goods are goods that are non-excludable (no one can be excluded from using them) and non-rivalrous, meaning that one person’s consumption does not prevent anyone else’s (non-rivalrous) (Smith, 2003; 475). Public goods are undersupplied by the market because there is no commercial incentive to produce them and thus require public provision or financing (Labonte, 2004). Health economists have long recognized 46 TAC listed fluconazole at R28.57 per 200mg capsule in the public sector, 80.24 in the private sector, and R1.78 in Thailand. 47 See www.tac.org.za and conduct a search on ‘fluconazole’ 48 Press release dated November 19, 2000 which indicates that TAC filed a Section 21 Exemption to the Medicines Control Council. 49 Press Release, dated November 28, 2000. www.tac.org.za 50 Correspondence on TAC website indicates that Morne Visser, TAC supporter and activist, brought in generic fluconazole on January 13,2001. 51 See: www.cptech.org/ip/health/fluconazole/info.html 52 The Agreement on Trade-Related Aspects of Intellectual Property contains provisions to allow countries to issue compulsory licenses or parallel import patented products in situations of a national emergency. 53 The African markets for pharmaceuticals are very small in comparison to European and North American markets, but have been steadily growing and the demand for pharmaceuticals is projected to increase substantially. that the provision of health care goods and services often results in a market failure. Market failure occurs when the market fails to efficiently allocate goods and services.54 The government intervenes to provide public goods either through direct public provision of the good, through taxation, financing, or licensing (Smith, 2003: 475). Classic examples of public goods are a lighthouse, peace, and security. Health products and services are also undersupplied as a result of government failure. Governments, particularly those in developing countries, often lack the fiscal or organizational capacity to provide for the health of their populations. Hence, the need arises for support from other actors to help promote and protect the health of these populations. Global public goods are goods whose benefits transcend borders, benefit all countries, population groups, and generations (Türmen, 1999: 9). Global public goods include clean air, and peace and security and can be supplied through transnational agreements and protocols and other forms of collective action (Barrett, 2004). At the global level, there is no equivalent institution with the power to levy taxes to provide public goods. Thus, the global public goods (GPG) concept is intended to provide a rationale and framework for collective action on global health issues. By demonstrating that health risks, particularly in the context of globalization (Türmen, 1999), transcend national borders; the GPG concept encourages the global community to support efforts for disease eradication, health promotion and health protection. The GPG concept is part of the agenda promoted by the United Nations Development Programme (UNDP) (Woodward et al, 2001) and serves as a framework for action, as well as a normative premise and a “paradigmatic shift in the conceptualization of public health” (Brando, 2004:11). Under the UNDP agenda, the GPG concept is intended to improve outcomes in global health as well provide intermediate products and services through collective action. There are various types of goods, including private goods, national public goods, intermediate public goods, and final global public goods (Kaul & Mendoza, 2003). Intermediate public goods are public goods that are non-excludable, but rivalrous (Brando, 2004). Intermediate public goods are seen to “bring us partially to the goal of global public health” (Brando, 2004:3), by providing health services and products that contribute to global health. Global public-private partnerships provide intermediate public goods, including disease surveillance, disease control, disease eradication or elimination, disease treatment, and resistance avoidance (Barrett, 2004a: 1). Ultimately, however, the pursuit of intermediate public goods through global public-private partnerships has several negative externalities for the attainment of global health outcomes and global cooperation in health. Global public-private partnerships are not global in design or implementation. The design and governance of GPPPs is highly asymmetrical, with governance of the GPPPs primarily residing in North American and Western European countries. While some GPPPs can claim that they have incorporated national health governance priorities and voices (for example, ACHAP) in the design and implementation of their programs, GPPPs continue to be criticized for the lack of representation and participation of southern stakeholders in both the design and governance of programs. GPPPs are intended to serve as a pathway to global health outcomes, yet ultimately may reinforce existing power and decision-making imbalances, rather than advancing true global cooperation in health. Global health governance should not serve as a euphemism for ‘northern’ health governance, and thus GPPPs offer little prospect in their current state for broader global health governance and cooperation. 54 Ensor, Tim. “Microeconomics and Market Failure in Health.” [on-line]. Accessed April 4, 2004. http://www1.worldbank.org/hnp/hsd/documents/MFailure.pdf Instead of contributing to greater global health cooperation, drug donation programs reinforce the charity model of health, and potentially intensify dependency relations. Few partnerships address state capacity building and health infrastructure development which would support developing states in providing for the health of their populations, and enhance their role in both national and global health governance. While some GPPPs train healthcare personnel and work with national and sub-national health governance authorities and institutions to provide a broader array of services, a large contingent of GPPPs provide vertical programs, which do not, in and of themselves, strengthen health systems. Indeed, these programs often entail significant costs, by requiring states to integrate programs into often overextended health systems. Thus, as an intermediate step towards global health cooperation, GPPPs offer much of the same in the way of existing power and social relations, and thus do not truly advance global health cooperation, but rather northern dominance and economic privilege in health governance. The intermediate goods and services that are provided by GPPPs are largely palliative; they do not address the underlying social determinants of health that render populations, particularly the poor, vulnerable to ill health. The World Health Organization defines health as “a state of complete physical, mental and social well-being and not merely the absence of disease or infirmity”55 In policy and practice, health interventions have largely been focused on the latter aspects of the definition. Disease and morbidity eradication have achieved primacy in our notions and evaluations of health as evidenced by the proliferation and increasing reliance on pharmaceutical and therapeutic interventions (drugs, chemical treatments, surgery, etc). The provision of intermediate public goods via global public-private partnerships contains a strong biomedical and technological bias; health interventions are overwhelmingly focused on providing remedies (drugs, health services, vaccines), but very little attention is devoted to health promotion via the social determinants of health. At best, they provide gender or population-sensitive solutions (for vulnerable or marginalized populations), but do not access the root causes of vulnerability to ill health which drive the expression of epidemics and infectious diseases. GPPPs, as a pathway towards global health outcomes, are conceivably matching epidemiological, but not necessarily social priorities of health. If the WHO’s definition is employed as a measure of the effectiveness of GPPPs in advancing global health outcomes, it is clear that they advance a narrow conceptualization of health, and in the case of pharmaceutical companies, advance their own interests for the continued reliance on drug interventions to support health. GPPPs might respond that it is not within their mandate to focus on the social determinants of health given their core competencies, and are only in a position to offer biomedical and technological solutions. Global and national health governance institutions are thus left with the task of addressing the most complex aspects of health. Without the attendant national and global health architecture to support and provide interventions to address the social determinants of health, GPPPs role as an intermediate institutional pathway to health leads global health governance largely into the management of illness rather than the promotion and protection of health. Finally, GPPPs do not necessarily include equity considerations in their program design and evaluation. Like the AAI, partnerships often choose countries that already have existing health infrastructure to administer and deliver their programs and products, and thus the poorest countries may be excluded (See Yamey, 2001 for a discussion of GAVI). Moreover, it is difficult to measure how equitably products and services are distributed within the country under partnership arrangements. Equity evaluations have been a critical oversight in the outcome and 55 World Health Organization (WHO) Constitution (www.who.int/about/definition/en/) Accessed November 19, 2005 evaluation orientations of GPPPs. As discussed earlier, most GPPPs lack a research or outcome orientation that goes beyond measuring the value-added aspect of the partnership, and fail to consider the negative externalities of partnership, including the potential for compounding health inequities. The global public goods concept has an inherent equity component, in that the goods must be non-excludable. Intermediate goods are non-excludable but rivalrous; however, GPPPs provide goods and services that are excludable. Global public-private partnerships have the potential to exacerbate health inequities, and thus as a ‘pathway’ to global health outcomes, may undermine global health equity. Global public-private partnerships provide life-saving and therapeutic interventions and resources for thousands of people and it is thus, at first blush, inconceivable to criticize them. However, evaluations of global public-private partnerships must incorporate normative and operational considerations, in addition to the value-added aspect, in order to carefully and thoughtfully evaluate their role in the emerging global health architecture. This discussion of the conceptualization of health is critical to global health cooperation; because how we conceptualize health will bear profound implications for the types of responses
that are employed. Historically, it has been difficult to obtain collective action for public goods.
The global public goods concept, as advanced by the UNDP, attempts to provide a framework
for collective action based on common need. The global public goods concept, however, does
little to advance a policy model based on entitlement or a human right to health. We need new
conceptions and theories of global health cooperation, including critical theories that question the
interests served by various discourses in the international normative order on health, as well as
conceptions of health that explore alternative frameworks for global health cooperation.

7. Conclusions and Recommendations

Given the operational and normative implications of global public-private partnerships for national and global health governance, what is the way forward? What are the implications for policy and practice surrounding GPPPs? Richter (2003) argues that UN agencies should abandon the public-private partnership paradigm altogether, while Buse & Waxman (2001) argue that a moratorium on GPPPs should be imposed while further research is conducted. Reforming GPPPs through transforming their research and outcome orientations would require the full cooperation of partners. At this point, the World Health Organization must develop a framework for the design, implementation, and evaluation of partnerships, including an equity evaluation component, as well as a component that addresses the interfaces of the partnership with national health governance. At minimum, partnerships must involve national health authorities in their design, implementation, and evaluation. Currently, partnerships often originate at the international level, potentially excluding developing states in these processes (Widdus, 2003). The question of who will monitor global public-private partnerships is a difficult one. Global health governance institutions are operating under tight budgets, and a solution does not immediately present itself. Relying on public-private partnerships to self-discipline and report seems unlikely. Therefore, the World Health Organization must exercise leadership in this domain, and appoint some form of oversight body/group to research and report on the partnerships. This would also include compiling and distributing information on best practices, lessons learned, and so forth. This paper has provided a preliminary investigation and analysis of some of the real and potential operational and normative implications of global public-private partnerships for national and global health governance and thus offers insight into some of the areas that require attention, and possibly reform. There are significant gaps in our knowledge about global public-private partnerships. Considerably more research needs to be conducted on the partnerships, particularly research about partnerships on the ground (Widdus, 2003). We need to develop criteria and measures of effectiveness for GPPPs to evaluate both the specific contributions of GPPPs to their stated objectives as well as for their contributions to global health goals and cooperation. Furthermore, it is important to challenge the functional narrative of partnerships by investigating and revealing the ethical, social, and normative underpinnings of partnerships. The knowledge deficit also applies to other institutions and actors of global health governance. While the literature contains a sufficient array of studies examining the individual
actors and institutions in global health governance, very few examine the interfaces, conflicts,
and methods of cooperation and integration among and between these actors and institutions.
Even fewer assess how these contradictions, conflicts, and cooperation affect national health
governance or the normative basis of global health governance. Globalization is the driving force
behind the emergence of global health governance, and global public-private partnerships give
evidence to the emergence of a global polity. Growing interconnectedness between states and
non-state actors in health has the potential to yield improvements in global health outcomes and
cooperation. However, dependency on private sector corporations and actors in global health
governance may also result in a weakening of efforts to hold them accountable for their practices
and actions (Richter, 2004). While it could be argued that these partnerships reflect the
inclination of corporations to become ‘good corporate citizens’ they are not in and of themselves
a proxy for good corporate citizenship in the global polity. Accordingly, there must be sufficient
research and oversight to evaluate and monitor their normative and operational contributions to
the emerging global health governance architecture.
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Source: http://www.cpsa-acsp.ca/papers-2006/Brown.pdf

1997 aavp program

American Association of Veterinary Parasitologists Saturday, July 19, 1997 4:45 (6) Development of a Swine Animal Peppermill Hotel & Casino Model Where Opportunistic Invasion of the Colon by Campylobacter jejuni Occurs Spontaneously 12:00-3:00 AAVP Board Meeting 1:00-8:00 Speaker Prep Refreshments 2:00 Registration - Ballroom Lobby 5:15 (7) Anthelmintic Use on Saskatc

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FORMULAIRE REGLEMENT PARTICULIER DE TOURNOI REGION LIEGE DE L'A.F.T. Document à compléter et à mettre sur www.tournoi.org lors de la demande de souscription en ligne de votre tournoi Ce document sera consulté par les affiliés lors de l'inscription en ligne à votre tournoi. Matricule club : Nom du club : Le tournoi se joue sous le patronage et selon les règles de l'A.F.

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