Readability of informed consent documents and its impact on consent refusal rate by Yash V. Kamath, Yashashri C. Shetty, Ishita C. Lanjewar, Ankita Kulkarni

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Research Ethics: Ideas and Practices of Russian Young Scientists by E. V. Popova, D. M. Matsepuro

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Gaps in the ethical governance of pharmaceutical clinical trials in Europe by Rosemarie D. L. C. Bernabe, Rosemarie D. L. C. Bernabe, Shereen A. Dawkins-Cox, Christine C. Gispen-de Wied

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A Retrospective Aspect at the Evaluations of a University Clinical Research Ethics Committee: The Unseen Reasons Behind the Disapproved Studies by Canan Uluoğlu, Ali Kağan Coşkun, Utku Aykan

Subjects: “…ethics committee…”
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Evaluating cognitive bias in clinical ethics supports: a scoping review by Louise Giaume, Antoine Lamblin, Nathalie Pinol, Frédérique Gignoux-Froment, Marion Trousselard

Subjects: “…Cognitive bias; Deliberation; Clinical ethical committees and supports…”
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Ethical aspects of clinical trials in Russia and BRICS countries: an overview by Sergey Y. Simeniv, Alexander L. Khokhlov, Olga N. Soldatova, Nathalia V. Pyatigorskaya

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Requirements and special considerations for drug trials with children across six jurisdictions: 2. Ethics review in the regulatory approval process by Breanne Stewart, Pirkko Lepola, Gunter F. Egger, Fahimeda Ali, Albert J. Allen, Albert J. Allen, Alysha K. Croker, Andrew J. Davidson, Pamela Dicks, Saul N. Faust, Saul N. Faust, Dionna Green, Collin Hovinga, Collin Hovinga, Agnes V. Klein, Robyn Langham, Hidefumi Nakamura, Laura Pioppo, Shiva Ramroop, Michiyo Sakiyama, Isabel Sanchez Vigil de la Villa, Junko Sato, Donna L. Snyder, Mark A. Turner, Mark A. Turner, Sarah Zaidi, Kanecia Zimmerman, Kanecia Zimmerman, Thierry Lacaze-Masmonteil

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