Suchergebnisse

This case is an example of using quantitative research on democracies, and it is based on my PhD study in political science. In the study, I used a comparative method, through a large-n, outcome-centric research design, to examine which factors affect the varying levels of the quality of democracy in the stable democracies around the world. This case study illustrates how a researcher can develop their research agenda from identifying the research subject to formulating the research question for the study. In the case, I describe different research steps that were used in my PhD study, such as how the research design was developed, how the operationalization of the concept quality of democracy was performed, how the theoretical model for explaining the variation in the quality of democracy was developed, and how the empirical analyses by using statistical analysis were performed. During the research journey, there were also several methodological challenges to handle, and in this case study, I also describe and comment on how I handled these challenges. As a pedagogical tool, the aim of this case is to be helpful in improving future research that uses a large-n research design and analyzes the data using statistical analysis.

This Article argues that pharmaceutical marketing to doctors should be more critically evaluated and entitled to less First Amendment protection, contrary to a trend dating back to the Supreme Court's 2011 decision in Sorrell. In particular, the Article argues that more information to doctors in the form of pharmaceutical marketing does not necessarily result in better patient outcomes. The Article adds a significant critique based on the existence and impact of cognitive bias literature that has thus far not been recognized in this area. If courts fully embrace this understanding, they should recognize that the government, through the Food and Drug Administration, has a right to limit statements that may encourage doctors to prescribe unapproved uses of drugs with potentially fatal consequences. This Article reveals that recent expansion of First Amendment jurisprudence is based on key cognitive biases and assumptions. First, courts, and even some doctors themselves, improperly assume that doctors are adequately sophisticated, such that doctors are protected from self-interested marketing, which this Article demonstrates as inconsistent with reality. Second, current case law assumes that the availability of more information necessarily promotes better decisions so long as it is not patently false, a proposition that this Article shows is especially unfounded in the unique market of prescription drugs. Importantly, such assumptions can have critical health consequences since they promote uses of drugs for which there is often inadequate scientific basis and serious health consequences. Finally, this Article builds upon the revealed cognitive biases to suggest empirically-informed changes to cabin the expansion of First Amendment protection of pharmaceutical marketing as well as broader structural reform. This Article proposes to treat potentially misleading information differently than entirely truthful speech, thus giving states greater discretion to regulate potentially misleading information. In addition, this Article proposes that the burden of proof in such cases should be reversed, so that courts will no longer consider disclaimers as a true alternative to speech restriction without proof that companies will actually promote more informed decisions. The Article also suggests structural changes to medical education, drug development, and marketing informed by the cognitive biases revealed here.

This Article provides valuable insight to the broader discussion of reforming investor-state disputes. Many have noted that the system is in a crisis due to a lack of democratic accountability and inconsistent decisions, which create a chilling effect on legitimate domestic law and policy. Despite substantial discussion in recent years concerning how to reform investor-state disputes, there is only limited discussion concerning the extent to which such disputes challenge domestic intellectual property (IP) limits, as well as global IP norms. Moreover, even among those who recognize the challenge to IP limits, the relevance of human rights is generally not addressed. This Article begins to fill this gap from two angles. First, it aims to promote a better understanding of how such disputes undermine the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) at an important time when policymakers are recommending reliance on policy space under TRIPS. Second, it considers whether human rights might help to protect this policy space using the facts of Eli Lilly v. Canada.

This Article provides valuable insight to the broader discussion of reforming investor-state disputes. Many have noted that the system is in a crisis due to a lack of democratic accountability and inconsistent decisions, which create a chilling effect on legitimate domestic law and policy. Despite substantial discussion in recent years concerning how to reform investor-state disputes, there is only limited discussion concerning the extent to which such disputes challenge domestic intellectual property (IP) limits, as well as global IP norms. Moreover, even among those who recognize the challenge to IP limits, the relevance of human rights is generally not addressed. This Article begins to fill this gap from two angles. First, it aims to promote a better understanding of how such disputes undermine the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) at an important time when policymakers are recommending reliance on policy space under TRIPS. Second, it considers whether human rights might help to protect this policy space using the facts of Eli Lilly v. Canada.