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  1. Research Ethics in the Context of Transition: Gaps in Policies and Programs on the Protection of Research Participants in the Selected Countries of Central and Eastern Europe.Andrei Famenka - 2016 - Science and Engineering Ethics 22 (6):1689-1706.
    This paper examines the ability of countries in Central and Eastern Europe to ensure appropriate protection of research participants in the field of increasingly globalizing biomedical research. By applying an analytical framework for identifying gaps in policies and programs for human subjects protection to four countries of CEE—Belarus, Latvia, Lithuania, and Poland, substantial gaps in the scope and content of relevant policies and major impediments to program performance have been revealed. In these countries, public policies on the protection of research (...)
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  • The evaluation of complex clinical trial protocols: resources available to research ethics committees and the use of clinical trial registries—a case study.Núria Homedes & Antonio Ugalde - 2015 - Journal of Medical Ethics 41 (6):464-469.
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  • Non-equivalent stringency of ethical review in the Baltic States: a sign of a systematic problem in Europe?E. Gefenas, V. Dranseika, A. Cekanauskaite, K. Hug, S. Mezinska, E. Peicius, V. Silis, A. Soosaar & M. Strosberg - 2010 - Journal of Medical Ethics 36 (7):435-439.
    We analyse the system of ethical review of human research in the Baltic States by introducing the principle of equivalent stringency of ethical review, that is, research projects imposing equal risks and inconveniences on research participants should be subjected to equally stringent review procedures. We examine several examples of non-equivalence or asymmetry in the system of ethical review of human research: (1) the asymmetry between rather strict regulations of clinical drug trials and relatively weaker regulations of other types of clinical (...)
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  • Broadening the “Infrastructure Effect”: Lessons from the Early Development of Research Ethics in Eastern Europe.Vilius Dranseika, Eugenijus Gefenas & Marcin Waligora - 2016 - American Journal of Bioethics 16 (6):26-28.
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  • Public awareness of and attitudes towards research biobanks in Latvia.S. Mezinska, J. Kaleja, I. Mileiko, D. Santare, V. Rovite & L. Tzivian - 2020 - BMC Medical Ethics 21 (1):1-11.
    BackgroundPublic awareness and engagement are among the main prerequisites for protecting the rights of research participants and for successful and sustainable functioning of research biobanks. The aim of our study was to analyse public awareness and attitudes towards research biobanks in Latvia, and to compare these data with the results of the 2010 Eurobarometer study. We also analysed the influence of awareness and attitudes towards biobanks on willingness to participate in biobank studies and on preferred type of informed consent.MethodsWe developed (...)
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  • (1 other version)Publication Ethics in Biomedical Journals from Countries in Central and Eastern Europe.Mindaugas Broga, Goran Mijaljica, Marcin Waligora, Aime Keis & Ana Marusic - 2014 - Science and Engineering Ethics 20 (1):99-109.
    Publication ethics is an important aspect of both the research and publication enterprises. It is particularly important in the field of biomedical science because published data may directly affect human health. In this article, we examine publication ethics policies in biomedical journals published in Central and Eastern Europe. We were interested in possible differences between East European countries that are members of the European Union and South-East European countries that are not members of the European Union. The most common ethical (...)
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