The ethical guidelines of the Ministry of Health, Labour and Welfare stipulate that when it is difficult to obtain informed consent from a research subject in medical research, an opportunity to refuse (opt-out) should be provided through disclosing information. This page contains information on medical research conducted at the Kyoto University Center for Genomic Medicine that requires the provision of an opportunity to refuse. Translated with www.DeepL.com/Translator (free version)
Existing samples and information collected through medical research conducted at our facility by the “Ethical Guidelines for Medical Research Involving Human Subjects” and the “Ethical Guidelines for Human Genome and Gene Analysis Research” issued by the Ministry of Health, Labour and Welfare may be used for new research at our center. Such research may involve cases in which it is difficult to obtain consent again from the research subject. In such a case, it is difficult to get the permission of the research subject again. The following does not apply to cases where re-consent has been obtained.