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Regulating international clinical research: an ethical framework for policy-makers
  1. Bernardo Aguilera1,
  2. David DeGrazia1,2,
  3. Annette Rid1
  1. 1Department of Bioethics, The Clinical Center, National Institutes of Health, Bethesda, Maryland, USA
  2. 2Department of Philosophy, George Washington University, Washington, DC, USA
  1. Correspondence to Dr Annette Rid; annette.rid{at}


The global distribution of clinical trials is shifting to low-income and middle-income countries (LMICs), and adequate regulations are essential for protecting the rights and interests of research participants in these countries. However, policy-makers in LMICs can face an ethical trade-off: stringent regulatory protections for participants can lead researchers or sponsors to conduct their research elsewhere, potentially depriving the local population of the opportunity to benefit from international clinical research. In this paper, we propose a three-step ethical framework that helps policy-makers to navigate this trade-off. We use a recent set of regulatory protections in Chile to illustrate the practical value of our proposed framework, providing original ethical analysis and previously unpublished data from Chile obtained through freedom of information requests.

  • health policy
  • health services research
  • clinical trial

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Summary box

  • The global distribution of clinical trials is shifting to low-income and middle-income countries (LMICs), and adequate regulations are essential for protecting research participants.

  • Policy-makers in LMICs often face an ethical trade-off: stringent regulatory protections can lead sponsors to conduct their research elsewhere, depriving LMICs of the potential benefits of international research.

  • We develop a three-step ethical framework to guide policy-makers in dealing with key ethical considerations involved in navigating this trade-off.

  • Using a recent set of regulatory protections in Chile, we illustrate the practical value of our proposed framework, providing original ethical analysis and previously unpublished data.

  • The proposed ethical framework helps policy-makers strike an appropriate balance between protecting research participants and reaping the benefits of appropriate clinical research.


The global distribution of clinical trials is changing. Trials are shifting to low-income and middle-income countries (LMICs), where markets are expanding; participants are easily recruited; and research costs remain low.1 2 This shift has raised concerns about sponsors and researchers ‘outsourcing’ trials and possibly taking unfair advantage of vulnerable populations.3 For example, some researchers from high-income countries (HICs) have been criticised for using ‘double standards’ by conducting trials in LMICs that would not be ethically approvable in their home countries, such as placebo-controlled trials that withhold or delay the best proven treatments.4 5

In response, some LMICs have introduced stringent regulatory protections for clinical trial participants. For example, in 2012, India required that sponsors provide free clinical care to participants injured during a trial, whether or not the injury was research-related.6 However, stringent protections can lead sponsors to conduct their research elsewhere, depriving LMICs of the potential benefits of hosting studies. In India, for instance, clinical trial registrations fell sharply after the new protections were introduced.6

At the time, the dominant reaction was negative: India might lose the benefits of international research.7 Indeed, international research is often regarded as an important means of improving infrastructure, training and enhancing economic activity in LMICs.8 9 Thus, the ethical challenge is to balance the goals of protecting research participants and reaping the benefits of appropriate clinical research.10 This paper explores Chile’s recent experience to address this issue and develops ethical guidance for policy-makers. While especially useful for policy-makers in LMICs, our proposed ethical framework can also guide policy-makers in HICs who seek to protect participants while promoting beneficial research.

Emerging economies and research regulation: the case of Chile

Clinical trials have expanded most rapidly in ‘emerging economies’, where appropriate healthcare infrastructure and skilled research workforces attract private sponsors.11–13 As an emerging economy with a high density of externally sponsored clinical trials,14 Chile helpfully illustrates how countries in the current landscape of international research face ethical trade-offs in clinical trial regulation.

Chile passed its first law on clinical research in 2006. Criticised for insufficiently focusing on ‘the protection of persons’,15 this law has been succeeded by further research regulations. In 2015, Law 20.850 introduced changes regarding compensation for research-related injuries and post-trial access to treatments that are remarkably stringent.16 As in other Latin American countries, the regulations are more stringent than international guidelines (table 1), indicating a regional trend towards greater protections for research participants.17

Table 1

Comparison of the WMA’s Declaration of Helsinki,59 the CIOMS‘s International Ethical Guidelines for Health-related Research Involving Humans21 and Chile’s Law 20.85016

Stricter protections, fewer trials?

Several Chilean parliament members and academics raised concerns that Law 20.850 might disincentivise clinical research.18 Data from the Chilean Institute of Public Health, obtained through freedom of information requests, seem to support these concerns. Based on the Institute’s mandatory registry of clinical trials involving investigational drugs, we found that the mean number of trials registered per year dropped from 95.5 (SD 6.9) before Law 20.850 was enacted to 75.8 (SD 6.2) (figure 1). The decline occurred mainly in phase 3/4 clinical trials, which decreased from an average of 71.2 (SD 2.9) between 2010 and 2015 to 53 (SD 6.9) between 2016 and 2019. Clinical trial sponsorship remained stable during both time periods, with a mean of 97% trials per year sponsored by pharmaceutical companies from outside Chile.

Figure 1

Number and phase of clinical trials registered in Chile between 2010 and 2019. Research sponsors are legally required to register all trials of drugs that have not been licensed by the Chilean Institute of Public Health (equivalent to the Food and Drug Administration in the USA) or are used outside their licensed indication. The arrow indicates when Chile’s Law 20.850 was enacted. The total number of trials (2010–2019) was N=876. Three trials (n=2 (2011), n=1 (2017)) were excluded since they were not reported as corresponding to phases 1–4. Data were obtained by freedom of information requests.

Can the new regulatory protections for participants explain this decline in international clinical research? This is a difficult question, as the absolute number of trials in Chile is low and our observation period is relatively short. Nonetheless, several considerations support a causal relationship.

The decrease in clinical trial numbers immediately followed the introduction of Law 20.850, with new trial registrations remaining below 87 annually, the lowest number of registrations observed in any of the previous years (figure 1). The sharpest decline has occurred in phase 3/4 clinical trials, for which the new regulatory protections are most relevant. Phase 3/4 trials can involve large numbers of participants, increasing the likelihood that sponsors must compensate for injuries. Study drugs are also more likely to prove beneficial in later trial phases, triggering post-trial access requirements. The increased prospect of substantial additional costs might have led sponsors to discontinue trials or move them to countries with less stringent regulatory protections, as occurred in India.10 Finally, other factors do not seem to explain the decline in clinical trial registrations in Chile. There was neither a wider downward trend in clinical research activity (indeed, global trial numbers have grown steadily in recent years19) nor wider economic or political instability in Chile that could have deterred research sponsors, and the Chilean clinical trial market is not yet considered saturated.20

Ethical trade-offs between protecting participants and reaping research benefits

Most laws and regulations have some negative consequences. In the present case, Law 20.850 might have disincentivised international research sponsors from registering new clinical trials in Chile. We recommend that policy-makers balance the goals of protecting research participants and reaping the benefits of appropriate clinical research using the following three-step framework (table 2). Using Law 20.850 as an example (table 1), we discuss how policy-makers should evaluate the need to revise existing protections.

Table 2

A three-step ethical framework for evaluating existing regulatory protections for clinical research

Supplemental material

Supplemental material

Step 1: do the regulatory protections have a sound ethical rationale?

Policy-makers should determine, first, whether the regulatory protections are prima facie ethically defensible. Are the protections consistent with widely accepted ethical standards for clinical research? Do they protect participants’ rights and interests, such as the right to be free of non-consensual experimentation or the interest in maintaining good health? Do the protections meet other ethical criteria, such as a just and fair distribution of research benefits and burdens?

A negative answer to all these questions provides a strong indication that the protections should be revised or revoked. For example, if a regulation excluded illiterate populations from research because of concerns about their decisional capacity, it should be revised. Because literacy is not necessary for making voluntary and informed decisions, excluding these populations prevents them from exercising their rights and, in some trials, promoting their interests by enrolling in potentially beneficial research. A blanket exclusion would also undermine principles of fair participant selection and conflict with recognised international guidelines.21 However, even in prima facie clear-cut cases, policy-makers should engage in an in-depth ethical analysis using our proposed framework. Such analysis can help to decide whether and how a given regulation should be revised, all things considered.

In the present case, the provision of compensation for research-related injuries and post-trial access to proven beneficial treatments are generally consistent with sound ethical standards. However, a careful analysis of Law 20.850 suggests that reasonable people would likely disagree about how the law should spell out these standards.

Law 20.850 requires research sponsors to obtain insurance that compensates for research-related injuries, ‘even when they result from facts or circumstances that could not have been foreseen or avoided according to the technical and scientific knowledge available at the time’.16 This ‘no-fault’ compensation scheme is widely considered ethically sound because it protects participants by reducing the harms of research-related injuries and helps to distribute research risks and potential benefits fairly.22 However, Law 20.850 goes beyond ‘no-fault’ compensation by stipulating that ‘once the injury is confirmed, it will be presumed that it was produced by the study’.16 The law only specifies that ‘the opportunity to prosecute … will expire ten years after the injury manifests’, leaving open the possibility of prosecuting injuries that manifest at any point after a study.16 These provisions arguably place an excessive burden on research sponsors, as they might be held liable for conditions that arise unrelated to the research.

Law 20.850 also mandates that sponsors provide participants the investigational treatment—or, at a later point, the licensed drug—‘free of charge and for as long as its therapeutic utility remains’ after the study has ended.16 These provisions are prima facie sound insofar as they protect the interests of patients and compensate for their participation in research. However, reasonable people might disagree as to whether the sole responsibility for providing post-trial access to treatments should be placed on sponsors. For example, when local authorities or institutions can contribute to ensuring post-trial access, the resulting burden on sponsors could reasonably be considered excessive. Moreover, it can be argued that the supply of effective treatments is sustainable only when sponsors and local actors actively engage in a collaborative partnership.23 24

In sum, while a prima facie case for Law 20.850 can be made, certain aspects of the protections it sets out can reasonably be considered to place excessive burdens on researchers and sponsors.

Step 2: what are the benefits and costs of implementing the regulatory protections?

After scrutinising the prima facie ethical case for the given regulatory protections, policy-makers should survey all the relevant facts regarding their effects. Specifically, policy-makers should examine systematically who benefits from the protections and who incurs costs, including how significant the benefits and costs are. We understand benefits and costs broadly: have the affected people fared better or worse after the protections were introduced, as compared with how they would have fared if the protections had not been enacted? This analysis should encompass everyone affected: not only research participants but also patients and the wider community who can receive benefits or incur costs from international clinical research (table 2).

We limit our discussion of Law 20.850 to the Chilean population, as this is the primary focus for Chilean policy-makers and the law’s global impact is less certain. However, depending on policy-makers’ needs, our framework can be applied on a national, regional, or global level.

Research participants

Although participants are the intended beneficiaries of Law 20.850, we are unaware of empirical data demonstrating that more participants have received appropriate compensation for research-related injuries or post-trial access to beneficial interventions. However, even assuming good-faith implementation of the law, it is unlikely that it made participants substantially better off than they otherwise would have been. Previous regulations already had a ‘no fault’ scheme of compensation for research-related injuries (though less stringent),25 and post-trial access to investigational drugs was authorised (though not required).26 Since no more than two-thirds of investigational drugs prove beneficial even in late-phase trials,27 this suggests that the law’s benefits to research participants are limited.

Potential research participants might be worse off if the decline in clinical trials following Law 20.850 deprived them from the benefits of enrolment. Yet evidence suggests that clinical outcomes are neither better nor worse in clinical trials than in routine care.28 Moreover, the Chilean healthcare system provides meaningful access to health services,29 so that potential participants’ clinical needs can reasonably be met outside the research context. And the financial compensation that potential participants might obtain by enrolling in research is typically small and limited to reimbursements for time or expenses incurred—particularly in phase 3/4 trials,30 which declined most sharply after Law 20.850 was introduced. Thus, it seems unlikely that the law made potential participants noticeably worse-off.

Conversely, potential participants might be better off if the decline in trials meant they incurred fewer research-related risks. While robust evidence on the psychological and social risks of participating in research is lacking, the risk of serious health-related harm is generally low in late-phase clinical trials.31 Taken together, this suggests that Law 20.850 has led to limited benefits for clinical trial participants. Additionally, the law has likely had no noticeable impact on potential participants who have been deprived of the opportunity to enrol in research.


Due to the decline in clinical trials following Law 20.850, patients might be worse off due to a reduced access to successful products. However, these costs to patients are likely limited. New drugs can be licensed in Chile whether or not they have undergone local testing.32 Moreover, even if local data were required for licensure, the research currently being conducted does not address patients’ most pressing health needs. According to our data, at most 13.5% of the trials registered in Chile between 2016 and 2019 addressed one of the top 10 causes of disability-adjusted life years in the country33 (table 3). Moreover, around 30% of investigational drugs that undergo pivotal trials in Latin America are not licensed in the countries where they are tested, and licensed products remain unaffordable for most of the local population.34

Table 3

Top 10 causes of death and disability combined in Chile,33 matched with the number and percentage of clinical trials that address the given cause between 2016 and 2019 (ie, after Law 20.850 was introduced)

Further, with a decline in clinical trial numbers, fewer patients might benefit from the improvements in clinical care that result from the organisational culture, systems and expertise fostered by research.35 However, in Chile, the associated costs are likely limited. Evidence about research-related improvements in clinical care comes mostly from HICs, which may be better equipped to implement quality improvements.36 Moreover, many reports of research-related clinical capacity building involve publicly funded trials.37 It is unclear to what extent private sponsors—which fund 97% of clinical trials in Chile—achieve similar results. Likewise, the decline in clinical trial numbers likely had no noticeable benefits for patients from research staff moving to provide routine clinical care, as Chile has no shortage of trained clinicans.38

Finally, patients might be worse off due to the decline in clinical trials and the resulting loss in research capacity building for the development of locally relevant drugs. Yet, only 2.5% of publications from externally sponsored trials in Chile list a local researcher as a coauthor, suggesting that local research involvement is limited.39 Moreover, according to our data, more than 70% of clinical trials in Chile are phase 3/4 trials. Because these trials test existing hypotheses, rather than generating new ones, they provide local researchers limited opportunities for developing their research skills.40 Indeed, Chilean researchers worry that local ‘efforts for building a scientific and entrepreneurial development in Chile would … be wiped out’ because the requirements of Law 20.850 are too difficult for local researchers and sponsors to meet.41

In sum, the decline in clinical trials after Law 20.850 was introduced does not seem to have led to major costs or harms for patients.

Wider population

The wider population might be worse off economically if Law 20.850 deprived them of clinical trial activity and the associated financial and economic benefits. Privately sponsored trials can provide drugs and services free of charge and thereby save costs for healthcare payers.42 43 While there is no corresponding evidence from Chile, we expect some such cost savings to occur. According to some reports from HICs, clinical research activities also significantly boost the national economy.44 45 In Chile, pharmaceutical industry sources claim that private investment is ‘annually around US$30 million in clinical studies and provides jobs to more than 2100 Chilean professionals and technicians’.46 Moreover, local healthcare professionals might receive compensation from pharmaceutical companies for recruiting participants.47 Law 20.850 therefore likely led to noticeable economic costs for the wider population. However, considering a labour force of >9 million people and a GDP of >$277 billion,48 these costs seem relatively small on a national scale.

Step 3: are the regulatory protections ethically justified, all things considered?

In the final step of our proposed framework, policy-makers should consider whether the given regulatory protections are, all things considered, ethically justified. While step 2 mostly involves descriptive fact-finding, step 3 involves ethical judgement in light of the relevant facts. Specifically, policy-makers should weigh the benefits of the given protections against the costs. They should then consider how these benefits and costs are distributed across different population groups, and to what extent that distribution creates new injustices or exacerbates existing ones—for example, by worsening the lot of the least advantaged in society.49 Finally, policy-makers should judge whether the costs to individuals or certain groups amount to a violation of their rights or vital moral safeguards, such as the right not to be exposed to risks and burdens that are disproportionate to the potential benefits of the research.50–55

If the benefits do not outweigh the costs, the protections create new injustices or exacerbate existing ones, or the protections violate the rights of individuals or certain groups, there is reason to revise or amend the protections. If, however, none of these ethical problems is evident and the protections’ benefits seem to outweigh the costs, then the protections are ethically justified. Table 4 provides examples of rights and justice considerations that are relevant for making these judgements. However, because rights and justice considerations are highly context-specific, policy-makers should carefully (and critically) consider the given legal, political and social contexts.

Table 4

Examples of rights and justice considerations when evaluating regulatory protections for clinical research

All things considered, our analysis suggests that the decline in clinical trials after Law 20.850 was introduced likely resulted in limited benefits to research participants and limited costs to patients, but noticeable costs to the wider population (online supplementary appendix 1). These findings support the common idea that LMICs can be made worse off by regulatory protections that disincentivise international clinical research, but with four important qualifications. First, since we did not conduct a formal cost–benefit analysis, our findings remain tentative. Second, both benefits and costs appear to be relatively small and might not be significant overall. This could be different in other countries, especially those with higher trial numbers. Third, in an emerging economy like Chile, costs resulting from fewer clinical trials seem to be mainly due to economic losses, instead of forgone benefits to participants and patients. Again, this could be different in other contexts, for example, resource-poorer LMICs where trials might help to meet basic health needs. Finally, both the benefits and costs of Law 20.850 could change over time. For example, clinical trial numbers might recover as sponsors adapt to the law, raising the question whether the limited aggregate costs during an expected transition period are a ‘price worth paying’ for the additional protections for participants.

Our findings also highlight the important fact that the benefits and costs of research regulations can be of multiple kinds and degrees, and that they are distributed across different populations. This brings out considerations of rights and justice. Partly because the benefits and costs of Law 20.850 are relatively small, our analysis does not suggest that it led to injustices or rights violations. However, where protections have more important benefits and costs, policy-makers should evaluate their distribution and moral significance by drawing on relevant notions of justice and rights.

Finally, our analysis raises concerns about how international clinical research in Chile is currently being conducted. Specifically, the costs of implementing Law 20.850 are limited mainly because the decline in clinical trials does not entail significant losses in research capacity building and research that is responsive to local health needs. This is cause for concern, given the potential of local research capacity to improve health and reduce health disparities in Chile.56

In sum, we believe that building a strong ethical case for revising Law 20.850 remains elusive. However, dispensing with those aspects of the law that can be reasonably considered too burdensome, while upholding appropriate protections regarding research-related injuries and post-trial access, might help to remove disincentives for conducting international clinical research in Chile. Any regulatory changes in this direction should ideally be associated with measures to actively promote local research capacity building and the conduct of research that is responsive to local health needs. For this to happen, Chilean policy-makers might strengthen research institutions, set clear research priorities, provide adequate research funding, and promote innovative partnerships with research sponsors.57


Policy-makers should be aware of the ethical trade-offs involved in regulating clinical research. We have proposed a three-step ethical framework for balancing the goals of protecting research participants and reaping the benefits of hosting clinical trials. This framework guides policy-makers in integrating key ethical and practical considerations, including which population groups are affected by a given set of regulatory protections, how different types of benefits and costs are distributed across these groups, and whether the rights of individuals or groups are being violated. Our framework could helpfully be expanded, for example, by further specifying notions of justice and rights, or incorporating elements of more formal cost–benefit analysis.58 However, policy-makers often have to make decisions with limited information and under time constraints. In this context, our framework provides useful ethical insights, which policy-makers might need to weigh with political or other considerations. Of note, although we use Chile as an illustrative example, our framework applies in LMICs as well as HICs and can be used to evaluate the need to revise existing protections with a national, regional or global scope. Similarly, the framework can be adapted so that policy-makers can evaluate new protections under consideration (online supplementary appendix 2).


Thanks to Benjamin Berkman, Alberto Lecaros, Joseph Millum, Christina Roadevin, Sofía Salas, Rodrigo Salinas and three anonymous reviewers for their help and comments during the preparation of this paper.



  • Handling editor Seye Abimbola

  • Twitter @bedobardo, @anetrid

  • Contributors BA and AR conceived the idea for the paper. BA acquired and analysed the data and wrote the first draft. AR and DDG revised the paper critically for important intellectual content. All authors approved of the final version and agreed to be accountable for all aspects of the work.

  • Funding This work was supported by the Clinical Center Department of Bioethics, which is in the Intramural Program of the National Institutes of Health.

  • Disclaimer The views expressed here are those of the authors and do not necessarily reflect the policies of the National Institutes of Health or the U.S. Department of Health and Human Services.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement The datasets analyzed during the current study are available from the authors on reasonable request.