- Post-trial period surveillance for randomised controlled cardiovascular studies: submitted protocols, consent forms and the role of the ethics board.M. I. Zia, R. Heslegrave & G. E. Newton - 2011 - Journal of Medical Ethics 37 (12):762-765.details
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Pharmaceutical Companies vs. the State: Who Is Responsible for Post-Trial Provision of Drugs in Brazil?Daniel Wei L. Wang & Octavio Luiz Motta Ferraz - 2012 - Journal of Law, Medicine and Ethics 40 (2):188-196.details
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Pharmaceutical Companies vs. the State: Who is Responsible for Post-Trial Provision of Drugs in Brazil?Daniel Wei L. Wang & Octavio Luiz Motta Ferraz - 2012 - Journal of Law, Medicine and Ethics 40 (2):188-196.details
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Reasons Why Post-Trial Access to Trial Drugs Should, or Need not be Ensured to Research Participants: A Systematic Review.N. Sofaer & D. Strech - 2011 - Public Health Ethics 4 (2):160-184.details
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Investigation of post-trial access views among study participants and stakeholders using photovoice and semistructured interviews.Nothando Ngwenya, Collins Iwuji, Nabeel Petersen, Nompilo Myeni, Samukelisiwe Nxumalo, Ursula Ngema & Janet Seeley - 2022 - Journal of Medical Ethics 48 (10):712-717.details
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Post‐trial obligations in the Declaration of Helsinki 2013: classification, reconstruction and interpretation.Ignacio Mastroleo - 2016 - Developing World Bioethics 16 (2):80-90.details
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Motives and risk perceptions of participants in a phase 1 trial for Hepatitis C Virus investigational therapy in pregnancy.Yasaswi Kislovskiy, Catherine Chappell, Emily Flaherty, Megan E. Hamm, Flor de Abril Cameron, Elizabeth Krans & Judy C. Chang - 2021 - Sage Publications Ltd: Research Ethics 18 (2):132-150.details
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Motives and risk perceptions of participants in a phase 1 trial for Hepatitis C Virus investigational therapy in pregnancy.Yasaswi Kislovskiy, Catherine Chappell, Emily Flaherty, Megan E. Hamm, Flor de Abril Cameron, Elizabeth Krans & Judy C. Chang - 2022 - Research Ethics 18 (2):132-150.details
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The Post-Research Ethical Obligations of the Research Enterprise in Developing Countries.Nida Khan - 2014 - Journal of Clinical Research and Bioethics 5 (4).details
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When the Trial Ends: The Case for Post-Trial Provisions in Clinical Psychedelic Research.Edward Jacobs, Ashleigh Murphy-Beiner, Ian Rouiller, David Nutt & Meg J. Spriggs - 2023 - Neuroethics 17 (1):1-17.details
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The clinical investigator-subject relationship: a contextual approach.David B. Resnik - 2009 - Philosophy, Ethics, and Humanities in Medicine 4:16-.details
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Post-trial access to study medication: a Brazilian e-survey with major stakeholders in clinical research.Sonia M. Dainesi & Moises Goldbaum - 2012 - Journal of Medical Ethics 38 (12):757-762.details
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Canadian research ethics board members’ attitudes toward benefits from clinical trials.Kori Cook, Jeremy Snyder & John Calvert - 2015 - BMC Medical Ethics 16 (1):1-7.details
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Attitudes toward Post‐Trial Access to Medical Interventions: A Review of Academic Literature, Legislation, and International Guidelines. [REVIEW]Kori Cook, Jeremy Snyder & John Calvert - 2015 - Developing World Bioethics 16 (2):70-79.details
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Marking Shifts in Human Research Ethics in the Development of Biobanking.D. Chalmers, M. Burgess, K. Edwards, J. Kaye, E. M. Meslin & D. Nicol - 2015 - Public Health Ethics 8 (1):63-71.details
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Human dignity as a basis for providing post-trial access to healthcare for research participants: a South African perspective.Pamela Andanda & Jane Wathuta - 2018 - Medicine, Health Care and Philosophy 21 (1):139-155.details
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Benefit Sharing – From Biodiversity to Human Genetics.Doris Schroeder & Julie Cook Lucas (eds.) - 2013 - Dordrecht, Netherlands: Springer.details
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Normative and Non-normative Concepts: Paternalism and Libertarian Paternalism.Kalle Grill - 2013 - In Daniel Strech, Irene Hirschberg & Georg Marckmann (eds.), Ethics in Public Health and Health Policy. Springer. pp. 27-46.details
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La obligación de continuidad de tratamiento beneficioso hacia los sujetos de investigación.Ignacio Mastroleo - 2012 - Dissertation, Universidad de Buenos Airesdetails
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Acceso post investigación obligatorio para los participantes de las investigaciones biomédicas: la discusión en torno al párrafo 30 de la Declaración de Helsinki.Ignacio Mastroleo - 2008 - Cuadernos de Trabajo Del Centro de Investigaciones Éticas 11:27-43.details
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